Component
Lycopene
Lycopene. Species, exposure and limitations are retained in each linked claim.
57 recorded relationships. Experimental role, claim status and evidence remain attached to each record.
How nutrients influence it
Every nutrient with a recorded effect on this component, credited to the nutrient that acted rather than the chapter that recorded it. Open a nutrient to see the findings and the conditions they were measured under.
Other things that act on it
Enzymes, hormones, genes, and other components with a recorded effect. These are not nutrients, so they do not count toward the arrows above. Each finding names the chapter that recorded it.
How nutrients reach it in more than one step
Chains of two or more recorded steps that end here, grouped by the nutrient they start from. Each step is a separate finding, so a chain is a route a mechanism could take, not proof that it does.
Tracing routes…
What it does
Every recorded relationship this component is part of, grouped by its role. Plain wording comes first; the technical statement follows.
What it acts on
Lycopene reduced IGF-I-stimulated AP-1 binding capacity in MCF7 cells.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/10798222.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "f9229468bbed86c3c4fdbb24f80d139f5cac41e1692195090d19a195bcd144e8", "start_char": 0, "end_char": 1731, "text_sha256": "f9229468bbed86c3c4fdbb24f80d139f5cac41e1692195090d19a195bcd144e8"}
- experimental_model
- Growth-factor stimulation and signaling assays
- exposure
- IGF-I stimulation with lycopene exposure
- limitations
- Cell-line mechanism; not proof of lowered human serum IGF-I or cancer treatment.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human MCF7 breast cancer cells
- plain_language
- A downstream gene-regulatory response also fell.
- primary_references
- [lycopene-p10798222] Lycopene interferes with cell cycle progression and insulin-like growth factor I signaling in mammary cancer cells. (2000). https://pubmed.ncbi.nlm.nih.gov/10798222/ DOI: 10.1207/s15327914nc3601_14
- tissue_or_cell_type
- IRS1 phosphorylation, AP-1 and cell cycle
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 676–687
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Growth-factor stimulation and signaling assays · source_derived_draft · unverified_draft
### lycopene-ap1 Lycopene reduced IGF-I-stimulated AP-1 binding capacity in MCF7 cells. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: A downstream gene-regulatory response also fell. organism: Human MCF7 breast cancer cells tissue_or_cell_type: IRS1 phosphorylation, AP-1 and cell cycle experimental_model: Growth-factor stimulation and signaling assays limitations: Cell-line mechanism; not proof of lowered human serum IGF-I or cancer treatment. exposure: IGF-I stimulation with lycopene exposure evidence_span: {"source_cache": "artifacts/lycopene-research/10798222.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "f9229468bbed86c3c4fdbb24f80d139f5cac41e1692195090d19a195bcd144e8", "start_char": 0, "end_char": 1731, "text_sha256": "f9229468bbed86c3c4fdbb24f80d139f5cac41e1692195090d19a195bcd144e8"} [lycopene-p10798222] Lycopene interferes with cell cycle progression and insulin-like growth factor I signaling in mammary cancer cells. (2000). https://pubmed.ncbi.nlm.nih.gov/10798222/ DOI: 10.1207/s15327914nc3601_14
Complete structured claim and evidenceLycopene treatment increased ARE-driven reporter expression in transfected cancer cells.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/15657364.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "a25b93d6074a1e560bf1e163aa70c511e99199b9bb62ccdffdbe70e51fcc7c32", "start_char": 0, "end_char": 1890, "text_sha256": "a25b93d6074a1e560bf1e163aa70c511e99199b9bb62ccdffdbe70e51fcc7c32"}
- experimental_model
- Reporter, expression and dominant-negative transcription-factor experiments
- exposure
- Lycopene and ethanolic derivative extract
- limitations
- Unidentified derivative extract was active; direct binding of intact lycopene to KEAP1 was not established.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human cancer cell cultures
- plain_language
- Cells activated a protective gene program in this experiment.
- primary_references
- [lycopene-p15657364] Carotenoids activate the antioxidant response element transcription system. (2005). https://pubmed.ncbi.nlm.nih.gov/15657364/ DOI: 10.1158/1535-7163.177.4.1
- tissue_or_cell_type
- ARE transcription and phase II enzyme expression
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 442–453
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Reporter, expression and dominant-negative transcription-factor experiments · source_derived_draft · unverified_draft
### lycopene-are-reporter Lycopene treatment increased ARE-driven reporter expression in transfected cancer cells. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: Cells activated a protective gene program in this experiment. organism: Human cancer cell cultures tissue_or_cell_type: ARE transcription and phase II enzyme expression experimental_model: Reporter, expression and dominant-negative transcription-factor experiments limitations: Unidentified derivative extract was active; direct binding of intact lycopene to KEAP1 was not established. exposure: Lycopene and ethanolic derivative extract evidence_span: {"source_cache": "artifacts/lycopene-research/15657364.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "a25b93d6074a1e560bf1e163aa70c511e99199b9bb62ccdffdbe70e51fcc7c32", "start_char": 0, "end_char": 1890, "text_sha256": "a25b93d6074a1e560bf1e163aa70c511e99199b9bb62ccdffdbe70e51fcc7c32"} [lycopene-p15657364] Carotenoids activate the antioxidant response element transcription system. (2005). https://pubmed.ncbi.nlm.nih.gov/15657364/ DOI: 10.1158/1535-7163.177.4.1
Complete structured claim and evidenceBasal nitric-oxide responses were unchanged in the CVD trial arm.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/24911964.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "d96a112b2d48544349cd136e7078ac9cdac3ecbedb41f2983db742b36e1cd8a9", "start_char": 0, "end_char": 1849, "text_sha256": "d96a112b2d48544349cd136e7078ac9cdac3ecbedb41f2983db742b36e1cd8a9"}
- experimental_model
- Double-blind placebo-controlled trial
- exposure
- 7 mg lycopene daily for two months
- limitations
- Surrogate physiology, not cardiovascular events; CVD and healthy populations analyzed separately.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human, 36 statin-treated CVD patients and 36 healthy volunteers
- plain_language
- Improved stimulated dilation did not establish a general rise in nitric oxide.
- primary_references
- [lycopene-p24911964] Effects of oral lycopene supplementation on vascular function in patients with cardiovascular disease and healthy volunteers: a randomised controlled trial. (2014). https://pubmed.ncbi.nlm.nih.gov/24911964/ DOI: 10.1371/journal.pone.0099070
- tissue_or_cell_type
- Forearm vascular responses
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 1001–1012
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Double-blind placebo-controlled trial · source_derived_draft · unverified_draft
### lycopene-basal-no-null Basal nitric-oxide responses were unchanged in the CVD trial arm. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: Improved stimulated dilation did not establish a general rise in nitric oxide. organism: Human, 36 statin-treated CVD patients and 36 healthy volunteers tissue_or_cell_type: Forearm vascular responses experimental_model: Double-blind placebo-controlled trial limitations: Surrogate physiology, not cardiovascular events; CVD and healthy populations analyzed separately. exposure: 7 mg lycopene daily for two months evidence_span: {"source_cache": "artifacts/lycopene-research/24911964.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "d96a112b2d48544349cd136e7078ac9cdac3ecbedb41f2983db742b36e1cd8a9", "start_char": 0, "end_char": 1849, "text_sha256": "d96a112b2d48544349cd136e7078ac9cdac3ecbedb41f2983db742b36e1cd8a9"} [lycopene-p24911964] Effects of oral lycopene supplementation on vascular function in patients with cardiovascular disease and healthy volunteers: a randomised controlled trial. (2014). https://pubmed.ncbi.nlm.nih.gov/24911964/ DOI: 10.1371/journal.pone.0099070
Complete structured claim and evidenceThe beta-carotene serum AUC did not differ when beta-carotene was taken alone or with lycopene.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/9278568.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "e318f6fef0bfed88403fa2adf46f9713ebddfe6ea586c29614e820442c57d056", "start_char": 0, "end_char": 1510, "text_sha256": "e318f6fef0bfed88403fa2adf46f9713ebddfe6ea586c29614e820442c57d056"}
- experimental_model
- Randomized-order double-blind crossover dosing experiment
- exposure
- 60 mg beta-carotene, 60 mg lycopene, or 60 mg of each together
- limitations
- Acute high-dose study; does not justify routine co-supplementation or establish universal competition rules.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human, ten healthy men
- plain_language
- The measured interaction was not symmetrical.
- primary_references
- [lycopene-p9278568] Ingestion by men of a combined dose of beta-carotene and lycopene does not affect the absorption of beta-carotene but improves that of lycopene. (1997). https://pubmed.ncbi.nlm.nih.gov/9278568/ DOI: 10.1093/jn/127.9.1833
- tissue_or_cell_type
- Serum carotenoid AUC over 24 hours
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 793–804
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Randomized-order double-blind crossover dosing experiment · source_derived_draft · unverified_draft
### lycopene-beta-carotene-response-null The beta-carotene serum AUC did not differ when beta-carotene was taken alone or with lycopene. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: The measured interaction was not symmetrical. organism: Human, ten healthy men tissue_or_cell_type: Serum carotenoid AUC over 24 hours experimental_model: Randomized-order double-blind crossover dosing experiment limitations: Acute high-dose study; does not justify routine co-supplementation or establish universal competition rules. exposure: 60 mg beta-carotene, 60 mg lycopene, or 60 mg of each together evidence_span: {"source_cache": "artifacts/lycopene-research/9278568.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "e318f6fef0bfed88403fa2adf46f9713ebddfe6ea586c29614e820442c57d056", "start_char": 0, "end_char": 1510, "text_sha256": "e318f6fef0bfed88403fa2adf46f9713ebddfe6ea586c29614e820442c57d056"} [lycopene-p9278568] Ingestion by men of a combined dose of beta-carotene and lycopene does not affect the absorption of beta-carotene but improves that of lycopene. (1997). https://pubmed.ncbi.nlm.nih.gov/9278568/ DOI: 10.1093/jn/127.9.1833
Complete structured claim and evidenceLycopene delayed cell-cycle progression without accompanying apoptotic or necrotic cell death in the tested MCF7 cultures.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/10798222.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "f9229468bbed86c3c4fdbb24f80d139f5cac41e1692195090d19a195bcd144e8", "start_char": 0, "end_char": 1731, "text_sha256": "f9229468bbed86c3c4fdbb24f80d139f5cac41e1692195090d19a195bcd144e8"}
- experimental_model
- Growth-factor stimulation and signaling assays
- exposure
- IGF-I stimulation with lycopene exposure
- limitations
- Cell-line mechanism; not proof of lowered human serum IGF-I or cancer treatment.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human MCF7 breast cancer cells
- plain_language
- Slower growth was distinguished from simply killing the cells.
- primary_references
- [lycopene-p10798222] Lycopene interferes with cell cycle progression and insulin-like growth factor I signaling in mammary cancer cells. (2000). https://pubmed.ncbi.nlm.nih.gov/10798222/ DOI: 10.1207/s15327914nc3601_14
- tissue_or_cell_type
- IRS1 phosphorylation, AP-1 and cell cycle
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 702–713
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Growth-factor stimulation and signaling assays · source_derived_draft · unverified_draft
### lycopene-cell-cycle Lycopene delayed cell-cycle progression without accompanying apoptotic or necrotic cell death in the tested MCF7 cultures. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: Slower growth was distinguished from simply killing the cells. organism: Human MCF7 breast cancer cells tissue_or_cell_type: IRS1 phosphorylation, AP-1 and cell cycle experimental_model: Growth-factor stimulation and signaling assays limitations: Cell-line mechanism; not proof of lowered human serum IGF-I or cancer treatment. exposure: IGF-I stimulation with lycopene exposure evidence_span: {"source_cache": "artifacts/lycopene-research/10798222.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "f9229468bbed86c3c4fdbb24f80d139f5cac41e1692195090d19a195bcd144e8", "start_char": 0, "end_char": 1731, "text_sha256": "f9229468bbed86c3c4fdbb24f80d139f5cac41e1692195090d19a195bcd144e8"} [lycopene-p10798222] Lycopene interferes with cell cycle progression and insulin-like growth factor I signaling in mammary cancer cells. (2000). https://pubmed.ncbi.nlm.nih.gov/10798222/ DOI: 10.1207/s15327914nc3601_14
Complete structured claim and evidenceThe alpha-tocopherol combination effect was not reproduced with beta-tocopherol, ascorbic acid or probucol.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/9784387.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "51bb94173c1f98ab622ff028dfefaa016eb3fb5021f40f79e1d7d02bceaa7c15", "start_char": 0, "end_char": 701, "text_sha256": "51bb94173c1f98ab622ff028dfefaa016eb3fb5021f40f79e1d7d02bceaa7c15"}
- experimental_model
- Combined-compound proliferation assay
- exposure
- Lycopene below 1 micromolar and alpha-tocopherol 50 micromolar
- limitations
- Reported in-vitro synergy; not proof of cancer prevention or a safe/effective supplement combination.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human DU-145 and PC-3 prostate carcinoma cells
- plain_language
- The result cannot be generalized to every antioxidant partner.
- primary_references
- [lycopene-p9784387] Lycopene in association with alpha-tocopherol inhibits at physiological concentrations proliferation of prostate carcinoma cells. (1998). https://pubmed.ncbi.nlm.nih.gov/9784387/ DOI: 10.1006/bbrc.1998.9351
- tissue_or_cell_type
- Cultured cell proliferation
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 884–895
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Combined-compound proliferation assay · source_derived_draft · unverified_draft
### lycopene-combination-specificity The alpha-tocopherol combination effect was not reproduced with beta-tocopherol, ascorbic acid or probucol. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: The result cannot be generalized to every antioxidant partner. organism: Human DU-145 and PC-3 prostate carcinoma cells tissue_or_cell_type: Cultured cell proliferation experimental_model: Combined-compound proliferation assay limitations: Reported in-vitro synergy; not proof of cancer prevention or a safe/effective supplement combination. exposure: Lycopene below 1 micromolar and alpha-tocopherol 50 micromolar evidence_span: {"source_cache": "artifacts/lycopene-research/9784387.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "51bb94173c1f98ab622ff028dfefaa016eb3fb5021f40f79e1d7d02bceaa7c15", "start_char": 0, "end_char": 701, "text_sha256": "51bb94173c1f98ab622ff028dfefaa016eb3fb5021f40f79e1d7d02bceaa7c15"} [lycopene-p9784387] Lycopene in association with alpha-tocopherol inhibits at physiological concentrations proliferation of prostate carcinoma cells. (1998). https://pubmed.ncbi.nlm.nih.gov/9784387/ DOI: 10.1006/bbrc.1998.9351
Complete structured claim and evidenceIn statin-treated CVD patients, lycopene improved endothelium-dependent vasodilation by 53% versus placebo, 95% CI 9% to 93%.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/24911964.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "d96a112b2d48544349cd136e7078ac9cdac3ecbedb41f2983db742b36e1cd8a9", "start_char": 0, "end_char": 1849, "text_sha256": "d96a112b2d48544349cd136e7078ac9cdac3ecbedb41f2983db742b36e1cd8a9"}
- experimental_model
- Double-blind placebo-controlled trial
- exposure
- 7 mg lycopene daily for two months
- limitations
- Surrogate physiology, not cardiovascular events; CVD and healthy populations analyzed separately.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human, 36 statin-treated CVD patients and 36 healthy volunteers
- plain_language
- A blood-vessel response improved in the patient group.
- primary_references
- [lycopene-p24911964] Effects of oral lycopene supplementation on vascular function in patients with cardiovascular disease and healthy volunteers: a randomised controlled trial. (2014). https://pubmed.ncbi.nlm.nih.gov/24911964/ DOI: 10.1371/journal.pone.0099070
- tissue_or_cell_type
- Forearm vascular responses
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 962–973
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Double-blind placebo-controlled trial · source_derived_draft · unverified_draft
### lycopene-cvd-edv In statin-treated CVD patients, lycopene improved endothelium-dependent vasodilation by 53% versus placebo, 95% CI 9% to 93%. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: A blood-vessel response improved in the patient group. organism: Human, 36 statin-treated CVD patients and 36 healthy volunteers tissue_or_cell_type: Forearm vascular responses experimental_model: Double-blind placebo-controlled trial limitations: Surrogate physiology, not cardiovascular events; CVD and healthy populations analyzed separately. exposure: 7 mg lycopene daily for two months evidence_span: {"source_cache": "artifacts/lycopene-research/24911964.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "d96a112b2d48544349cd136e7078ac9cdac3ecbedb41f2983db742b36e1cd8a9", "start_char": 0, "end_char": 1849, "text_sha256": "d96a112b2d48544349cd136e7078ac9cdac3ecbedb41f2983db742b36e1cd8a9"} [lycopene-p24911964] Effects of oral lycopene supplementation on vascular function in patients with cardiovascular disease and healthy volunteers: a randomised controlled trial. (2014). https://pubmed.ncbi.nlm.nih.gov/24911964/ DOI: 10.1371/journal.pone.0099070
Complete structured claim and evidenceEndothelium-independent vasodilation did not change with lycopene in the CVD trial arm.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/24911964.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "d96a112b2d48544349cd136e7078ac9cdac3ecbedb41f2983db742b36e1cd8a9", "start_char": 0, "end_char": 1849, "text_sha256": "d96a112b2d48544349cd136e7078ac9cdac3ecbedb41f2983db742b36e1cd8a9"}
- experimental_model
- Double-blind placebo-controlled trial
- exposure
- 7 mg lycopene daily for two months
- limitations
- Surrogate physiology, not cardiovascular events; CVD and healthy populations analyzed separately.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human, 36 statin-treated CVD patients and 36 healthy volunteers
- plain_language
- The trial distinguished different ways blood vessels relax.
- primary_references
- [lycopene-p24911964] Effects of oral lycopene supplementation on vascular function in patients with cardiovascular disease and healthy volunteers: a randomised controlled trial. (2014). https://pubmed.ncbi.nlm.nih.gov/24911964/ DOI: 10.1371/journal.pone.0099070
- tissue_or_cell_type
- Forearm vascular responses
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 988–999
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Double-blind placebo-controlled trial · source_derived_draft · unverified_draft
### lycopene-eidv-null Endothelium-independent vasodilation did not change with lycopene in the CVD trial arm. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: The trial distinguished different ways blood vessels relax. organism: Human, 36 statin-treated CVD patients and 36 healthy volunteers tissue_or_cell_type: Forearm vascular responses experimental_model: Double-blind placebo-controlled trial limitations: Surrogate physiology, not cardiovascular events; CVD and healthy populations analyzed separately. exposure: 7 mg lycopene daily for two months evidence_span: {"source_cache": "artifacts/lycopene-research/24911964.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "d96a112b2d48544349cd136e7078ac9cdac3ecbedb41f2983db742b36e1cd8a9", "start_char": 0, "end_char": 1849, "text_sha256": "d96a112b2d48544349cd136e7078ac9cdac3ecbedb41f2983db742b36e1cd8a9"} [lycopene-p24911964] Effects of oral lycopene supplementation on vascular function in patients with cardiovascular disease and healthy volunteers: a randomised controlled trial. (2014). https://pubmed.ncbi.nlm.nih.gov/24911964/ DOI: 10.1371/journal.pone.0099070
Complete structured claim and evidenceLycopene at 0.1 micromolar stimulated gap-junction communication in human fetal skin fibroblasts.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/10620348.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "dfd11c7c19dcd07e092a601ff44e9c900b5ecd717d3661ac2aca48d5cac72011", "start_char": 0, "end_char": 1295, "text_sha256": "dfd11c7c19dcd07e092a601ff44e9c900b5ecd717d3661ac2aca48d5cac72011"}
- experimental_model
- Gap-junction and promoter/mRNA assays
- exposure
- Lycopene 0.1 micromolar; acyclo-retinoic acid 1 or 50 micromolar depending on endpoint
- limitations
- Communication, mRNA stability and RAR reporter responses are distinct; very high metabolite doses are not physiological proof.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human fetal skin fibroblasts and reporter systems
- plain_language
- Neighboring cells exchanged small signals more readily in this model.
- primary_references
- [lycopene-p10620348] Stimulation of gap junctional communication: comparison of acyclo-retinoic acid and lycopene. (2000). https://pubmed.ncbi.nlm.nih.gov/10620348/ DOI: 10.1006/abbi.1999.1510
- tissue_or_cell_type
- Connexin-related intercellular communication
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 611–622
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Gap-junction and promoter/mRNA assays · source_derived_draft · unverified_draft
### lycopene-gap-junction Lycopene at 0.1 micromolar stimulated gap-junction communication in human fetal skin fibroblasts. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: Neighboring cells exchanged small signals more readily in this model. organism: Human fetal skin fibroblasts and reporter systems tissue_or_cell_type: Connexin-related intercellular communication experimental_model: Gap-junction and promoter/mRNA assays limitations: Communication, mRNA stability and RAR reporter responses are distinct; very high metabolite doses are not physiological proof. exposure: Lycopene 0.1 micromolar; acyclo-retinoic acid 1 or 50 micromolar depending on endpoint evidence_span: {"source_cache": "artifacts/lycopene-research/10620348.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "dfd11c7c19dcd07e092a601ff44e9c900b5ecd717d3661ac2aca48d5cac72011", "start_char": 0, "end_char": 1295, "text_sha256": "dfd11c7c19dcd07e092a601ff44e9c900b5ecd717d3661ac2aca48d5cac72011"} [lycopene-p10620348] Stimulation of gap junctional communication: comparison of acyclo-retinoic acid and lycopene. (2000). https://pubmed.ncbi.nlm.nih.gov/10620348/ DOI: 10.1006/abbi.1999.1510
Complete structured claim and evidenceLycopene at 0.1 micromolar was inactive in the connexin-43 mRNA-stabilization assay.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/10620348.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "dfd11c7c19dcd07e092a601ff44e9c900b5ecd717d3661ac2aca48d5cac72011", "start_char": 0, "end_char": 1295, "text_sha256": "dfd11c7c19dcd07e092a601ff44e9c900b5ecd717d3661ac2aca48d5cac72011"}
- experimental_model
- Gap-junction and promoter/mRNA assays
- exposure
- Lycopene 0.1 micromolar; acyclo-retinoic acid 1 or 50 micromolar depending on endpoint
- limitations
- Communication, mRNA stability and RAR reporter responses are distinct; very high metabolite doses are not physiological proof.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human fetal skin fibroblasts and reporter systems
- plain_language
- Improved communication does not establish every proposed connexin mechanism.
- primary_references
- [lycopene-p10620348] Stimulation of gap junctional communication: comparison of acyclo-retinoic acid and lycopene. (2000). https://pubmed.ncbi.nlm.nih.gov/10620348/ DOI: 10.1006/abbi.1999.1510
- tissue_or_cell_type
- Connexin-related intercellular communication
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 624–635
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Gap-junction and promoter/mRNA assays · source_derived_draft · unverified_draft
### lycopene-gja1-stability-null Lycopene at 0.1 micromolar was inactive in the connexin-43 mRNA-stabilization assay. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: Improved communication does not establish every proposed connexin mechanism. organism: Human fetal skin fibroblasts and reporter systems tissue_or_cell_type: Connexin-related intercellular communication experimental_model: Gap-junction and promoter/mRNA assays limitations: Communication, mRNA stability and RAR reporter responses are distinct; very high metabolite doses are not physiological proof. exposure: Lycopene 0.1 micromolar; acyclo-retinoic acid 1 or 50 micromolar depending on endpoint evidence_span: {"source_cache": "artifacts/lycopene-research/10620348.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "dfd11c7c19dcd07e092a601ff44e9c900b5ecd717d3661ac2aca48d5cac72011", "start_char": 0, "end_char": 1295, "text_sha256": "dfd11c7c19dcd07e092a601ff44e9c900b5ecd717d3661ac2aca48d5cac72011"} [lycopene-p10620348] Stimulation of gap junctional communication: comparison of acyclo-retinoic acid and lycopene. (2000). https://pubmed.ncbi.nlm.nih.gov/10620348/ DOI: 10.1006/abbi.1999.1510
Complete structured claim and evidenceSupplementation reduced CETP activity in HDL2 and HDL3 fractions.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/35978954.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "ed024b652760ea2f5ab124162690901b3e88995ea9648bea05b59f240de08c3a", "start_char": 0, "end_char": 2778, "text_sha256": "ed024b652760ea2f5ab124162690901b3e88995ea9648bea05b59f240de08c3a"}
- experimental_model
- Randomized diet/supplement trial biomarker analysis
- exposure
- Low tomato control; 224-350 mg/week food lycopene; or 70 mg/week supplement
- limitations
- Food and supplement doses differ; enzyme activities and particle sizes are surrogate endpoints, not proof of fewer events.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human, 225 adults aged 40-65 years
- plain_language
- A lipid-transfer measurement changed without proving the whole pathway is beneficial.
- primary_references
- [lycopene-p35978954] Lycopene-rich diets modulate HDL functionality and associated inflammatory markers without affecting lipoprotein size and distribution in moderately overweight, disease-free, middle-aged adults: A randomized controlled trial. (2022). https://pubmed.ncbi.nlm.nih.gov/35978954/ DOI: 10.3389/fnut.2022.954593
- tissue_or_cell_type
- HDL fractions and plasma lipoproteins
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 1040–1051
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Randomized diet/supplement trial biomarker analysis · source_derived_draft · unverified_draft
### lycopene-hdl-cetp Supplementation reduced CETP activity in HDL2 and HDL3 fractions. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: A lipid-transfer measurement changed without proving the whole pathway is beneficial. organism: Human, 225 adults aged 40-65 years tissue_or_cell_type: HDL fractions and plasma lipoproteins experimental_model: Randomized diet/supplement trial biomarker analysis limitations: Food and supplement doses differ; enzyme activities and particle sizes are surrogate endpoints, not proof of fewer events. exposure: Low tomato control; 224-350 mg/week food lycopene; or 70 mg/week supplement evidence_span: {"source_cache": "artifacts/lycopene-research/35978954.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "ed024b652760ea2f5ab124162690901b3e88995ea9648bea05b59f240de08c3a", "start_char": 0, "end_char": 2778, "text_sha256": "ed024b652760ea2f5ab124162690901b3e88995ea9648bea05b59f240de08c3a"} [lycopene-p35978954] Lycopene-rich diets modulate HDL functionality and associated inflammatory markers without affecting lipoprotein size and distribution in moderately overweight, disease-free, middle-aged adults: A randomized controlled trial. (2022). https://pubmed.ncbi.nlm.nih.gov/35978954/ DOI: 10.3389/fnut.2022.954593
Complete structured claim and evidenceThe lycopene-supplement arm increased HDL3-associated LCAT activity.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/35978954.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "ed024b652760ea2f5ab124162690901b3e88995ea9648bea05b59f240de08c3a", "start_char": 0, "end_char": 2778, "text_sha256": "ed024b652760ea2f5ab124162690901b3e88995ea9648bea05b59f240de08c3a"}
- experimental_model
- Randomized diet/supplement trial biomarker analysis
- exposure
- Low tomato control; 224-350 mg/week food lycopene; or 70 mg/week supplement
- limitations
- Food and supplement doses differ; enzyme activities and particle sizes are surrogate endpoints, not proof of fewer events.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human, 225 adults aged 40-65 years
- plain_language
- A cholesterol-handling enzyme changed in this fraction.
- primary_references
- [lycopene-p35978954] Lycopene-rich diets modulate HDL functionality and associated inflammatory markers without affecting lipoprotein size and distribution in moderately overweight, disease-free, middle-aged adults: A randomized controlled trial. (2022). https://pubmed.ncbi.nlm.nih.gov/35978954/ DOI: 10.3389/fnut.2022.954593
- tissue_or_cell_type
- HDL fractions and plasma lipoproteins
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 1027–1038
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Randomized diet/supplement trial biomarker analysis · source_derived_draft · unverified_draft
### lycopene-hdl-lcat The lycopene-supplement arm increased HDL3-associated LCAT activity. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: A cholesterol-handling enzyme changed in this fraction. organism: Human, 225 adults aged 40-65 years tissue_or_cell_type: HDL fractions and plasma lipoproteins experimental_model: Randomized diet/supplement trial biomarker analysis limitations: Food and supplement doses differ; enzyme activities and particle sizes are surrogate endpoints, not proof of fewer events. exposure: Low tomato control; 224-350 mg/week food lycopene; or 70 mg/week supplement evidence_span: {"source_cache": "artifacts/lycopene-research/35978954.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "ed024b652760ea2f5ab124162690901b3e88995ea9648bea05b59f240de08c3a", "start_char": 0, "end_char": 2778, "text_sha256": "ed024b652760ea2f5ab124162690901b3e88995ea9648bea05b59f240de08c3a"} [lycopene-p35978954] Lycopene-rich diets modulate HDL functionality and associated inflammatory markers without affecting lipoprotein size and distribution in moderately overweight, disease-free, middle-aged adults: A randomized controlled trial. (2022). https://pubmed.ncbi.nlm.nih.gov/35978954/ DOI: 10.3389/fnut.2022.954593
Complete structured claim and evidenceBoth lycopene intervention routes increased serum and HDL3-associated PON1 activity.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/35978954.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "ed024b652760ea2f5ab124162690901b3e88995ea9648bea05b59f240de08c3a", "start_char": 0, "end_char": 2778, "text_sha256": "ed024b652760ea2f5ab124162690901b3e88995ea9648bea05b59f240de08c3a"}
- experimental_model
- Randomized diet/supplement trial biomarker analysis
- exposure
- Low tomato control; 224-350 mg/week food lycopene; or 70 mg/week supplement
- limitations
- Food and supplement doses differ; enzyme activities and particle sizes are surrogate endpoints, not proof of fewer events.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human, 225 adults aged 40-65 years
- plain_language
- The activity of an enzyme carried by HDL changed.
- primary_references
- [lycopene-p35978954] Lycopene-rich diets modulate HDL functionality and associated inflammatory markers without affecting lipoprotein size and distribution in moderately overweight, disease-free, middle-aged adults: A randomized controlled trial. (2022). https://pubmed.ncbi.nlm.nih.gov/35978954/ DOI: 10.3389/fnut.2022.954593
- tissue_or_cell_type
- HDL fractions and plasma lipoproteins
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 1014–1025
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Randomized diet/supplement trial biomarker analysis · source_derived_draft · unverified_draft
### lycopene-hdl-pon1 Both lycopene intervention routes increased serum and HDL3-associated PON1 activity. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: The activity of an enzyme carried by HDL changed. organism: Human, 225 adults aged 40-65 years tissue_or_cell_type: HDL fractions and plasma lipoproteins experimental_model: Randomized diet/supplement trial biomarker analysis limitations: Food and supplement doses differ; enzyme activities and particle sizes are surrogate endpoints, not proof of fewer events. exposure: Low tomato control; 224-350 mg/week food lycopene; or 70 mg/week supplement evidence_span: {"source_cache": "artifacts/lycopene-research/35978954.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "ed024b652760ea2f5ab124162690901b3e88995ea9648bea05b59f240de08c3a", "start_char": 0, "end_char": 2778, "text_sha256": "ed024b652760ea2f5ab124162690901b3e88995ea9648bea05b59f240de08c3a"} [lycopene-p35978954] Lycopene-rich diets modulate HDL functionality and associated inflammatory markers without affecting lipoprotein size and distribution in moderately overweight, disease-free, middle-aged adults: A randomized controlled trial. (2022). https://pubmed.ncbi.nlm.nih.gov/35978954/ DOI: 10.3389/fnut.2022.954593
Complete structured claim and evidenceLycopene interventions reduced HDL3-associated serum amyloid A.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/35978954.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "ed024b652760ea2f5ab124162690901b3e88995ea9648bea05b59f240de08c3a", "start_char": 0, "end_char": 2778, "text_sha256": "ed024b652760ea2f5ab124162690901b3e88995ea9648bea05b59f240de08c3a"}
- experimental_model
- Randomized diet/supplement trial biomarker analysis
- exposure
- Low tomato control; 224-350 mg/week food lycopene; or 70 mg/week supplement
- limitations
- Food and supplement doses differ; enzyme activities and particle sizes are surrogate endpoints, not proof of fewer events.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human, 225 adults aged 40-65 years
- plain_language
- An HDL-associated inflammatory marker decreased.
- primary_references
- [lycopene-p35978954] Lycopene-rich diets modulate HDL functionality and associated inflammatory markers without affecting lipoprotein size and distribution in moderately overweight, disease-free, middle-aged adults: A randomized controlled trial. (2022). https://pubmed.ncbi.nlm.nih.gov/35978954/ DOI: 10.3389/fnut.2022.954593
- tissue_or_cell_type
- HDL fractions and plasma lipoproteins
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 1053–1064
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Randomized diet/supplement trial biomarker analysis · source_derived_draft · unverified_draft
### lycopene-hdl-saa Lycopene interventions reduced HDL3-associated serum amyloid A. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: An HDL-associated inflammatory marker decreased. organism: Human, 225 adults aged 40-65 years tissue_or_cell_type: HDL fractions and plasma lipoproteins experimental_model: Randomized diet/supplement trial biomarker analysis limitations: Food and supplement doses differ; enzyme activities and particle sizes are surrogate endpoints, not proof of fewer events. exposure: Low tomato control; 224-350 mg/week food lycopene; or 70 mg/week supplement evidence_span: {"source_cache": "artifacts/lycopene-research/35978954.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "ed024b652760ea2f5ab124162690901b3e88995ea9648bea05b59f240de08c3a", "start_char": 0, "end_char": 2778, "text_sha256": "ed024b652760ea2f5ab124162690901b3e88995ea9648bea05b59f240de08c3a"} [lycopene-p35978954] Lycopene-rich diets modulate HDL functionality and associated inflammatory markers without affecting lipoprotein size and distribution in moderately overweight, disease-free, middle-aged adults: A randomized controlled trial. (2022). https://pubmed.ncbi.nlm.nih.gov/35978954/ DOI: 10.3389/fnut.2022.954593
Complete structured claim and evidenceHealthy volunteers did not show an improvement in endothelium-dependent vasodilation after lycopene.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/24911964.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "d96a112b2d48544349cd136e7078ac9cdac3ecbedb41f2983db742b36e1cd8a9", "start_char": 0, "end_char": 1849, "text_sha256": "d96a112b2d48544349cd136e7078ac9cdac3ecbedb41f2983db742b36e1cd8a9"}
- experimental_model
- Double-blind placebo-controlled trial
- exposure
- 7 mg lycopene daily for two months
- limitations
- Surrogate physiology, not cardiovascular events; CVD and healthy populations analyzed separately.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human, 36 statin-treated CVD patients and 36 healthy volunteers
- plain_language
- The finding was not universal across participants.
- primary_references
- [lycopene-p24911964] Effects of oral lycopene supplementation on vascular function in patients with cardiovascular disease and healthy volunteers: a randomised controlled trial. (2014). https://pubmed.ncbi.nlm.nih.gov/24911964/ DOI: 10.1371/journal.pone.0099070
- tissue_or_cell_type
- Forearm vascular responses
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 975–986
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Double-blind placebo-controlled trial · source_derived_draft · unverified_draft
### lycopene-healthy-edv-null Healthy volunteers did not show an improvement in endothelium-dependent vasodilation after lycopene. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: The finding was not universal across participants. organism: Human, 36 statin-treated CVD patients and 36 healthy volunteers tissue_or_cell_type: Forearm vascular responses experimental_model: Double-blind placebo-controlled trial limitations: Surrogate physiology, not cardiovascular events; CVD and healthy populations analyzed separately. exposure: 7 mg lycopene daily for two months evidence_span: {"source_cache": "artifacts/lycopene-research/24911964.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "d96a112b2d48544349cd136e7078ac9cdac3ecbedb41f2983db742b36e1cd8a9", "start_char": 0, "end_char": 1849, "text_sha256": "d96a112b2d48544349cd136e7078ac9cdac3ecbedb41f2983db742b36e1cd8a9"} [lycopene-p24911964] Effects of oral lycopene supplementation on vascular function in patients with cardiovascular disease and healthy volunteers: a randomised controlled trial. (2014). https://pubmed.ncbi.nlm.nih.gov/24911964/ DOI: 10.1371/journal.pone.0099070
Complete structured claim and evidenceCancer prevalence on repeat biopsy was similar between groups.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/26422197.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "1327af281ec573be44c88b10fc7973e82e4963aab7bef3f7d14122e6c2a3dbea", "start_char": 0, "end_char": 1542, "text_sha256": "1327af281ec573be44c88b10fc7973e82e4963aab7bef3f7d14122e6c2a3dbea"}
- experimental_model
- Randomized six-month repeat-biopsy trial
- exposure
- Tomato extract containing 30 mg/day lycopene versus placebo
- limitations
- Small surrogate-endpoint study; exploratory histological extent findings were not established cancer prevention.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human, 58 completers with high-grade prostatic intraepithelial neoplasia
- plain_language
- This trial did not demonstrate cancer prevention.
- primary_references
- [lycopene-p26422197] A Phase II Randomized Trial of Lycopene-Rich Tomato Extract Among Men with High-Grade Prostatic Intraepithelial Neoplasia. (2015). https://pubmed.ncbi.nlm.nih.gov/26422197/ DOI: 10.1080/01635581.2015.1075560
- tissue_or_cell_type
- Serum biomarkers and prostate biopsies
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 1170–1181
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Randomized six-month repeat-biopsy trial · source_derived_draft · unverified_draft
### lycopene-hgp-cancer-null Cancer prevalence on repeat biopsy was similar between groups. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: This trial did not demonstrate cancer prevention. organism: Human, 58 completers with high-grade prostatic intraepithelial neoplasia tissue_or_cell_type: Serum biomarkers and prostate biopsies experimental_model: Randomized six-month repeat-biopsy trial limitations: Small surrogate-endpoint study; exploratory histological extent findings were not established cancer prevention. exposure: Tomato extract containing 30 mg/day lycopene versus placebo evidence_span: {"source_cache": "artifacts/lycopene-research/26422197.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "1327af281ec573be44c88b10fc7973e82e4963aab7bef3f7d14122e6c2a3dbea", "start_char": 0, "end_char": 1542, "text_sha256": "1327af281ec573be44c88b10fc7973e82e4963aab7bef3f7d14122e6c2a3dbea"} [lycopene-p26422197] A Phase II Randomized Trial of Lycopene-Rich Tomato Extract Among Men with High-Grade Prostatic Intraepithelial Neoplasia. (2015). https://pubmed.ncbi.nlm.nih.gov/26422197/ DOI: 10.1080/01635581.2015.1075560
Complete structured claim and evidenceSerum IGF-I and IGF-binding protein 3 did not meaningfully differ between groups.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/26422197.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "1327af281ec573be44c88b10fc7973e82e4963aab7bef3f7d14122e6c2a3dbea", "start_char": 0, "end_char": 1542, "text_sha256": "1327af281ec573be44c88b10fc7973e82e4963aab7bef3f7d14122e6c2a3dbea"}
- experimental_model
- Randomized six-month repeat-biopsy trial
- exposure
- Tomato extract containing 30 mg/day lycopene versus placebo
- limitations
- Small surrogate-endpoint study; exploratory histological extent findings were not established cancer prevention.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human, 58 completers with high-grade prostatic intraepithelial neoplasia
- plain_language
- Cell-culture IGF signaling findings did not translate into these blood measurements.
- primary_references
- [lycopene-p26422197] A Phase II Randomized Trial of Lycopene-Rich Tomato Extract Among Men with High-Grade Prostatic Intraepithelial Neoplasia. (2015). https://pubmed.ncbi.nlm.nih.gov/26422197/ DOI: 10.1080/01635581.2015.1075560
- tissue_or_cell_type
- Serum biomarkers and prostate biopsies
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 1144–1155
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Randomized six-month repeat-biopsy trial · source_derived_draft · unverified_draft
### lycopene-hgp-igf-null Serum IGF-I and IGF-binding protein 3 did not meaningfully differ between groups. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: Cell-culture IGF signaling findings did not translate into these blood measurements. organism: Human, 58 completers with high-grade prostatic intraepithelial neoplasia tissue_or_cell_type: Serum biomarkers and prostate biopsies experimental_model: Randomized six-month repeat-biopsy trial limitations: Small surrogate-endpoint study; exploratory histological extent findings were not established cancer prevention. exposure: Tomato extract containing 30 mg/day lycopene versus placebo evidence_span: {"source_cache": "artifacts/lycopene-research/26422197.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "1327af281ec573be44c88b10fc7973e82e4963aab7bef3f7d14122e6c2a3dbea", "start_char": 0, "end_char": 1542, "text_sha256": "1327af281ec573be44c88b10fc7973e82e4963aab7bef3f7d14122e6c2a3dbea"} [lycopene-p26422197] A Phase II Randomized Trial of Lycopene-Rich Tomato Extract Among Men with High-Grade Prostatic Intraepithelial Neoplasia. (2015). https://pubmed.ncbi.nlm.nih.gov/26422197/ DOI: 10.1080/01635581.2015.1075560
Complete structured claim and evidenceNo meaningful between-group PSA difference appeared after six months.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/26422197.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "1327af281ec573be44c88b10fc7973e82e4963aab7bef3f7d14122e6c2a3dbea", "start_char": 0, "end_char": 1542, "text_sha256": "1327af281ec573be44c88b10fc7973e82e4963aab7bef3f7d14122e6c2a3dbea"}
- experimental_model
- Randomized six-month repeat-biopsy trial
- exposure
- Tomato extract containing 30 mg/day lycopene versus placebo
- limitations
- Small surrogate-endpoint study; exploratory histological extent findings were not established cancer prevention.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human, 58 completers with high-grade prostatic intraepithelial neoplasia
- plain_language
- A prostate blood marker did not show a meaningful benefit.
- primary_references
- [lycopene-p26422197] A Phase II Randomized Trial of Lycopene-Rich Tomato Extract Among Men with High-Grade Prostatic Intraepithelial Neoplasia. (2015). https://pubmed.ncbi.nlm.nih.gov/26422197/ DOI: 10.1080/01635581.2015.1075560
- tissue_or_cell_type
- Serum biomarkers and prostate biopsies
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 1131–1142
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Randomized six-month repeat-biopsy trial · source_derived_draft · unverified_draft
### lycopene-hgp-psa-null No meaningful between-group PSA difference appeared after six months. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: A prostate blood marker did not show a meaningful benefit. organism: Human, 58 completers with high-grade prostatic intraepithelial neoplasia tissue_or_cell_type: Serum biomarkers and prostate biopsies experimental_model: Randomized six-month repeat-biopsy trial limitations: Small surrogate-endpoint study; exploratory histological extent findings were not established cancer prevention. exposure: Tomato extract containing 30 mg/day lycopene versus placebo evidence_span: {"source_cache": "artifacts/lycopene-research/26422197.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "1327af281ec573be44c88b10fc7973e82e4963aab7bef3f7d14122e6c2a3dbea", "start_char": 0, "end_char": 1542, "text_sha256": "1327af281ec573be44c88b10fc7973e82e4963aab7bef3f7d14122e6c2a3dbea"} [lycopene-p26422197] A Phase II Randomized Trial of Lycopene-Rich Tomato Extract Among Men with High-Grade Prostatic Intraepithelial Neoplasia. (2015). https://pubmed.ncbi.nlm.nih.gov/26422197/ DOI: 10.1080/01635581.2015.1075560
Complete structured claim and evidenceSerum lycopene rose 0.55 micromolar with tomato extract and fell 0.29 micromolar with placebo.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/26422197.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "1327af281ec573be44c88b10fc7973e82e4963aab7bef3f7d14122e6c2a3dbea", "start_char": 0, "end_char": 1542, "text_sha256": "1327af281ec573be44c88b10fc7973e82e4963aab7bef3f7d14122e6c2a3dbea"}
- experimental_model
- Randomized six-month repeat-biopsy trial
- exposure
- Tomato extract containing 30 mg/day lycopene versus placebo
- limitations
- Small surrogate-endpoint study; exploratory histological extent findings were not established cancer prevention.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human, 58 completers with high-grade prostatic intraepithelial neoplasia
- plain_language
- The intervention clearly changed exposure.
- primary_references
- [lycopene-p26422197] A Phase II Randomized Trial of Lycopene-Rich Tomato Extract Among Men with High-Grade Prostatic Intraepithelial Neoplasia. (2015). https://pubmed.ncbi.nlm.nih.gov/26422197/ DOI: 10.1080/01635581.2015.1075560
- tissue_or_cell_type
- Serum biomarkers and prostate biopsies
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 1118–1129
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Randomized six-month repeat-biopsy trial · source_derived_draft · unverified_draft
### lycopene-hgp-serum Serum lycopene rose 0.55 micromolar with tomato extract and fell 0.29 micromolar with placebo. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: The intervention clearly changed exposure. organism: Human, 58 completers with high-grade prostatic intraepithelial neoplasia tissue_or_cell_type: Serum biomarkers and prostate biopsies experimental_model: Randomized six-month repeat-biopsy trial limitations: Small surrogate-endpoint study; exploratory histological extent findings were not established cancer prevention. exposure: Tomato extract containing 30 mg/day lycopene versus placebo evidence_span: {"source_cache": "artifacts/lycopene-research/26422197.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "1327af281ec573be44c88b10fc7973e82e4963aab7bef3f7d14122e6c2a3dbea", "start_char": 0, "end_char": 1542, "text_sha256": "1327af281ec573be44c88b10fc7973e82e4963aab7bef3f7d14122e6c2a3dbea"} [lycopene-p26422197] A Phase II Randomized Trial of Lycopene-Rich Tomato Extract Among Men with High-Grade Prostatic Intraepithelial Neoplasia. (2015). https://pubmed.ncbi.nlm.nih.gov/26422197/ DOI: 10.1080/01635581.2015.1075560
Complete structured claim and evidenceProstate epithelial MCM-2 and p27 expression did not differ between treatment groups.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/26422197.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "1327af281ec573be44c88b10fc7973e82e4963aab7bef3f7d14122e6c2a3dbea", "start_char": 0, "end_char": 1542, "text_sha256": "1327af281ec573be44c88b10fc7973e82e4963aab7bef3f7d14122e6c2a3dbea"}
- experimental_model
- Randomized six-month repeat-biopsy trial
- exposure
- Tomato extract containing 30 mg/day lycopene versus placebo
- limitations
- Small surrogate-endpoint study; exploratory histological extent findings were not established cancer prevention.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human, 58 completers with high-grade prostatic intraepithelial neoplasia
- plain_language
- These tissue growth markers did not respond detectably.
- primary_references
- [lycopene-p26422197] A Phase II Randomized Trial of Lycopene-Rich Tomato Extract Among Men with High-Grade Prostatic Intraepithelial Neoplasia. (2015). https://pubmed.ncbi.nlm.nih.gov/26422197/ DOI: 10.1080/01635581.2015.1075560
- tissue_or_cell_type
- Serum biomarkers and prostate biopsies
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 1157–1168
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Randomized six-month repeat-biopsy trial · source_derived_draft · unverified_draft
### lycopene-hgp-tissue-null Prostate epithelial MCM-2 and p27 expression did not differ between treatment groups. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: These tissue growth markers did not respond detectably. organism: Human, 58 completers with high-grade prostatic intraepithelial neoplasia tissue_or_cell_type: Serum biomarkers and prostate biopsies experimental_model: Randomized six-month repeat-biopsy trial limitations: Small surrogate-endpoint study; exploratory histological extent findings were not established cancer prevention. exposure: Tomato extract containing 30 mg/day lycopene versus placebo evidence_span: {"source_cache": "artifacts/lycopene-research/26422197.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "1327af281ec573be44c88b10fc7973e82e4963aab7bef3f7d14122e6c2a3dbea", "start_char": 0, "end_char": 1542, "text_sha256": "1327af281ec573be44c88b10fc7973e82e4963aab7bef3f7d14122e6c2a3dbea"} [lycopene-p26422197] A Phase II Randomized Trial of Lycopene-Rich Tomato Extract Among Men with High-Grade Prostatic Intraepithelial Neoplasia. (2015). https://pubmed.ncbi.nlm.nih.gov/26422197/ DOI: 10.1080/01635581.2015.1075560
Complete structured claim and evidenceLycopene increased membrane-associated IGF-binding proteins without changing IGF-I receptor number or affinity.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/10798222.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "f9229468bbed86c3c4fdbb24f80d139f5cac41e1692195090d19a195bcd144e8", "start_char": 0, "end_char": 1731, "text_sha256": "f9229468bbed86c3c4fdbb24f80d139f5cac41e1692195090d19a195bcd144e8"}
- experimental_model
- Growth-factor stimulation and signaling assays
- exposure
- IGF-I stimulation with lycopene exposure
- limitations
- Cell-line mechanism; not proof of lowered human serum IGF-I or cancer treatment.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human MCF7 breast cancer cells
- plain_language
- The experiment points to altered signal regulation rather than fewer receptors.
- primary_references
- [lycopene-p10798222] Lycopene interferes with cell cycle progression and insulin-like growth factor I signaling in mammary cancer cells. (2000). https://pubmed.ncbi.nlm.nih.gov/10798222/ DOI: 10.1207/s15327914nc3601_14
- tissue_or_cell_type
- IRS1 phosphorylation, AP-1 and cell cycle
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 689–700
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Growth-factor stimulation and signaling assays · source_derived_draft · unverified_draft
### lycopene-igfbp Lycopene increased membrane-associated IGF-binding proteins without changing IGF-I receptor number or affinity. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: The experiment points to altered signal regulation rather than fewer receptors. organism: Human MCF7 breast cancer cells tissue_or_cell_type: IRS1 phosphorylation, AP-1 and cell cycle experimental_model: Growth-factor stimulation and signaling assays limitations: Cell-line mechanism; not proof of lowered human serum IGF-I or cancer treatment. exposure: IGF-I stimulation with lycopene exposure evidence_span: {"source_cache": "artifacts/lycopene-research/10798222.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "f9229468bbed86c3c4fdbb24f80d139f5cac41e1692195090d19a195bcd144e8", "start_char": 0, "end_char": 1731, "text_sha256": "f9229468bbed86c3c4fdbb24f80d139f5cac41e1692195090d19a195bcd144e8"} [lycopene-p10798222] Lycopene interferes with cell cycle progression and insulin-like growth factor I signaling in mammary cancer cells. (2000). https://pubmed.ncbi.nlm.nih.gov/10798222/ DOI: 10.1207/s15327914nc3601_14
Complete structured claim and evidenceLycopene reduced IGF-I-stimulated IRS1 tyrosine phosphorylation in MCF7 cells.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/10798222.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "f9229468bbed86c3c4fdbb24f80d139f5cac41e1692195090d19a195bcd144e8", "start_char": 0, "end_char": 1731, "text_sha256": "f9229468bbed86c3c4fdbb24f80d139f5cac41e1692195090d19a195bcd144e8"}
- experimental_model
- Growth-factor stimulation and signaling assays
- exposure
- IGF-I stimulation with lycopene exposure
- limitations
- Cell-line mechanism; not proof of lowered human serum IGF-I or cancer treatment.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human MCF7 breast cancer cells
- plain_language
- The growth signal was weaker at an intracellular relay.
- primary_references
- [lycopene-p10798222] Lycopene interferes with cell cycle progression and insulin-like growth factor I signaling in mammary cancer cells. (2000). https://pubmed.ncbi.nlm.nih.gov/10798222/ DOI: 10.1207/s15327914nc3601_14
- tissue_or_cell_type
- IRS1 phosphorylation, AP-1 and cell cycle
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 663–674
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Growth-factor stimulation and signaling assays · source_derived_draft · unverified_draft
### lycopene-irs1 Lycopene reduced IGF-I-stimulated IRS1 tyrosine phosphorylation in MCF7 cells. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: The growth signal was weaker at an intracellular relay. organism: Human MCF7 breast cancer cells tissue_or_cell_type: IRS1 phosphorylation, AP-1 and cell cycle experimental_model: Growth-factor stimulation and signaling assays limitations: Cell-line mechanism; not proof of lowered human serum IGF-I or cancer treatment. exposure: IGF-I stimulation with lycopene exposure evidence_span: {"source_cache": "artifacts/lycopene-research/10798222.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "f9229468bbed86c3c4fdbb24f80d139f5cac41e1692195090d19a195bcd144e8", "start_char": 0, "end_char": 1731, "text_sha256": "f9229468bbed86c3c4fdbb24f80d139f5cac41e1692195090d19a195bcd144e8"} [lycopene-p10798222] Lycopene interferes with cell cycle progression and insulin-like growth factor I signaling in mammary cancer cells. (2000). https://pubmed.ncbi.nlm.nih.gov/10798222/ DOI: 10.1207/s15327914nc3601_14
Complete structured claim and evidenceApproximately 79% ± 9% of plasma lycopene was associated with LDL in seven participants.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/7562097.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "a8e551bad4ddb5e7eb7d3c8d796a94532e7f4701e891d9daae92a44bfb04179b", "start_char": 0, "end_char": 1620, "text_sha256": "a8e551bad4ddb5e7eb7d3c8d796a94532e7f4701e891d9daae92a44bfb04179b"}
- experimental_model
- Plasma lipoprotein fractionation and ex-vivo incubation
- exposure
- Native plasma distributions and incubation experiments
- limitations
- Small descriptive study; distribution is not proof that raising LDL improves delivery or health.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human, seven normolipidemic participants
- plain_language
- Lycopene travels with blood lipoproteins; a blood measurement also reflects its carriers.
- primary_references
- [lycopene-p7562097] Distributions of carotenoids and alpha-tocopherol among lipoproteins do not change when human plasma is incubated in vitro. (1995). https://pubmed.ncbi.nlm.nih.gov/7562097/ DOI: 10.1093/jn/125.10.2610
- tissue_or_cell_type
- Plasma LDL, HDL and VLDL
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 247–258
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Plasma lipoprotein fractionation and ex-vivo incubation · source_derived_draft · unverified_draft
### lycopene-ldl-carriage Approximately 79% ± 9% of plasma lycopene was associated with LDL in seven participants. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: Lycopene travels with blood lipoproteins; a blood measurement also reflects its carriers. organism: Human, seven normolipidemic participants tissue_or_cell_type: Plasma LDL, HDL and VLDL experimental_model: Plasma lipoprotein fractionation and ex-vivo incubation limitations: Small descriptive study; distribution is not proof that raising LDL improves delivery or health. exposure: Native plasma distributions and incubation experiments evidence_span: {"source_cache": "artifacts/lycopene-research/7562097.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "a8e551bad4ddb5e7eb7d3c8d796a94532e7f4701e891d9daae92a44bfb04179b", "start_char": 0, "end_char": 1620, "text_sha256": "a8e551bad4ddb5e7eb7d3c8d796a94532e7f4701e891d9daae92a44bfb04179b"} [lycopene-p7562097] Distributions of carotenoids and alpha-tocopherol among lipoproteins do not change when human plasma is incubated in vitro. (1995). https://pubmed.ncbi.nlm.nih.gov/7562097/ DOI: 10.1093/jn/125.10.2610
Complete structured claim and evidenceLipoprotein subclass distributions and sizes did not change with the interventions.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/35978954.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "ed024b652760ea2f5ab124162690901b3e88995ea9648bea05b59f240de08c3a", "start_char": 0, "end_char": 2778, "text_sha256": "ed024b652760ea2f5ab124162690901b3e88995ea9648bea05b59f240de08c3a"}
- experimental_model
- Randomized diet/supplement trial biomarker analysis
- exposure
- Low tomato control; 224-350 mg/week food lycopene; or 70 mg/week supplement
- limitations
- Food and supplement doses differ; enzyme activities and particle sizes are surrogate endpoints, not proof of fewer events.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human, 225 adults aged 40-65 years
- plain_language
- Changes in enzyme activity were not the same as changes in particle size.
- primary_references
- [lycopene-p35978954] Lycopene-rich diets modulate HDL functionality and associated inflammatory markers without affecting lipoprotein size and distribution in moderately overweight, disease-free, middle-aged adults: A randomized controlled trial. (2022). https://pubmed.ncbi.nlm.nih.gov/35978954/ DOI: 10.3389/fnut.2022.954593
- tissue_or_cell_type
- HDL fractions and plasma lipoproteins
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 1066–1077
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Randomized diet/supplement trial biomarker analysis · source_derived_draft · unverified_draft
### lycopene-lipoprotein-size-null Lipoprotein subclass distributions and sizes did not change with the interventions. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: Changes in enzyme activity were not the same as changes in particle size. organism: Human, 225 adults aged 40-65 years tissue_or_cell_type: HDL fractions and plasma lipoproteins experimental_model: Randomized diet/supplement trial biomarker analysis limitations: Food and supplement doses differ; enzyme activities and particle sizes are surrogate endpoints, not proof of fewer events. exposure: Low tomato control; 224-350 mg/week food lycopene; or 70 mg/week supplement evidence_span: {"source_cache": "artifacts/lycopene-research/35978954.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "ed024b652760ea2f5ab124162690901b3e88995ea9648bea05b59f240de08c3a", "start_char": 0, "end_char": 2778, "text_sha256": "ed024b652760ea2f5ab124162690901b3e88995ea9648bea05b59f240de08c3a"} [lycopene-p35978954] Lycopene-rich diets modulate HDL functionality and associated inflammatory markers without affecting lipoprotein size and distribution in moderately overweight, disease-free, middle-aged adults: A randomized controlled trial. (2022). https://pubmed.ncbi.nlm.nih.gov/35978954/ DOI: 10.3389/fnut.2022.954593
Complete structured claim and evidenceLycopene-containing diets increased intestinal ISX expression relative to the vitamin-A-deficient control group.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/37269907.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "36b39754d4d3b4ed8721a15f8dffe03bfd387dcbef3ff50918daabb45c48e756", "start_char": 0, "end_char": 1986, "text_sha256": "36b39754d4d3b4ed8721a15f8dffe03bfd387dcbef3ff50918daabb45c48e756"}
- experimental_model
- Carotenoid-enzyme knockout comparison and vitamin-A diet experiment
- exposure
- 1 mg lycopene in cottonseed oil daily for two weeks; separate vitamin-A-deficient versus sufficient diets
- limitations
- Mouse knockout distribution does not directly quantify human cleavage; increased ISX signaling does not prove conversion to vitamin A.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Mouse
- plain_language
- Carotenoid exposure intersected a vitamin-A-responsive regulatory system.
- primary_references
- [lycopene-p37269907] Lycopene Accumulation in Transgenic Mice Lacking One or Both Carotenoid Cleaving Enzymes. (2023). https://pubmed.ncbi.nlm.nih.gov/37269907/ DOI: 10.1016/j.tjnut.2023.05.025
- tissue_or_cell_type
- Liver, other tissues and intestinal gene expression
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 845–856
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Carotenoid-enzyme knockout comparison and vitamin-A diet experiment · source_derived_draft · unverified_draft
### lycopene-mouse-isx Lycopene-containing diets increased intestinal ISX expression relative to the vitamin-A-deficient control group. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: Carotenoid exposure intersected a vitamin-A-responsive regulatory system. organism: Mouse tissue_or_cell_type: Liver, other tissues and intestinal gene expression experimental_model: Carotenoid-enzyme knockout comparison and vitamin-A diet experiment limitations: Mouse knockout distribution does not directly quantify human cleavage; increased ISX signaling does not prove conversion to vitamin A. exposure: 1 mg lycopene in cottonseed oil daily for two weeks; separate vitamin-A-deficient versus sufficient diets evidence_span: {"source_cache": "artifacts/lycopene-research/37269907.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "36b39754d4d3b4ed8721a15f8dffe03bfd387dcbef3ff50918daabb45c48e756", "start_char": 0, "end_char": 1986, "text_sha256": "36b39754d4d3b4ed8721a15f8dffe03bfd387dcbef3ff50918daabb45c48e756"} [lycopene-p37269907] Lycopene Accumulation in Transgenic Mice Lacking One or Both Carotenoid Cleaving Enzymes. (2023). https://pubmed.ncbi.nlm.nih.gov/37269907/ DOI: 10.1016/j.tjnut.2023.05.025
Complete structured claim and evidenceLycopene was enriched three- to fivefold in hepatic mitochondria compared with total hepatic content across the tested genotypes.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/37269907.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "36b39754d4d3b4ed8721a15f8dffe03bfd387dcbef3ff50918daabb45c48e756", "start_char": 0, "end_char": 1986, "text_sha256": "36b39754d4d3b4ed8721a15f8dffe03bfd387dcbef3ff50918daabb45c48e756"}
- experimental_model
- Carotenoid-enzyme knockout comparison and vitamin-A diet experiment
- exposure
- 1 mg lycopene in cottonseed oil daily for two weeks; separate vitamin-A-deficient versus sufficient diets
- limitations
- Mouse knockout distribution does not directly quantify human cleavage; increased ISX signaling does not prove conversion to vitamin A.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Mouse
- plain_language
- Location inside the cell matters as well as the total amount.
- primary_references
- [lycopene-p37269907] Lycopene Accumulation in Transgenic Mice Lacking One or Both Carotenoid Cleaving Enzymes. (2023). https://pubmed.ncbi.nlm.nih.gov/37269907/ DOI: 10.1016/j.tjnut.2023.05.025
- tissue_or_cell_type
- Liver, other tissues and intestinal gene expression
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 832–843
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Carotenoid-enzyme knockout comparison and vitamin-A diet experiment · source_derived_draft · unverified_draft
### lycopene-mouse-mitochondria Lycopene was enriched three- to fivefold in hepatic mitochondria compared with total hepatic content across the tested genotypes. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: Location inside the cell matters as well as the total amount. organism: Mouse tissue_or_cell_type: Liver, other tissues and intestinal gene expression experimental_model: Carotenoid-enzyme knockout comparison and vitamin-A diet experiment limitations: Mouse knockout distribution does not directly quantify human cleavage; increased ISX signaling does not prove conversion to vitamin A. exposure: 1 mg lycopene in cottonseed oil daily for two weeks; separate vitamin-A-deficient versus sufficient diets evidence_span: {"source_cache": "artifacts/lycopene-research/37269907.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "36b39754d4d3b4ed8721a15f8dffe03bfd387dcbef3ff50918daabb45c48e756", "start_char": 0, "end_char": 1986, "text_sha256": "36b39754d4d3b4ed8721a15f8dffe03bfd387dcbef3ff50918daabb45c48e756"} [lycopene-p37269907] Lycopene Accumulation in Transgenic Mice Lacking One or Both Carotenoid Cleaving Enzymes. (2023). https://pubmed.ncbi.nlm.nih.gov/37269907/ DOI: 10.1016/j.tjnut.2023.05.025
Complete structured claim and evidenceCarotenoid treatment promoted Nrf2 nuclear translocation, including colocalization with PML nuclear bodies.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/15657364.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "a25b93d6074a1e560bf1e163aa70c511e99199b9bb62ccdffdbe70e51fcc7c32", "start_char": 0, "end_char": 1890, "text_sha256": "a25b93d6074a1e560bf1e163aa70c511e99199b9bb62ccdffdbe70e51fcc7c32"}
- experimental_model
- Reporter, expression and dominant-negative transcription-factor experiments
- exposure
- Lycopene and ethanolic derivative extract
- limitations
- Unidentified derivative extract was active; direct binding of intact lycopene to KEAP1 was not established.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human cancer cell cultures
- plain_language
- The transcription factor moved toward the compartment where it can affect genes.
- primary_references
- [lycopene-p15657364] Carotenoids activate the antioxidant response element transcription system. (2005). https://pubmed.ncbi.nlm.nih.gov/15657364/ DOI: 10.1158/1535-7163.177.4.1
- tissue_or_cell_type
- ARE transcription and phase II enzyme expression
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 455–466
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Reporter, expression and dominant-negative transcription-factor experiments · source_derived_draft · unverified_draft
### lycopene-nrf2-location Carotenoid treatment promoted Nrf2 nuclear translocation, including colocalization with PML nuclear bodies. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: The transcription factor moved toward the compartment where it can affect genes. organism: Human cancer cell cultures tissue_or_cell_type: ARE transcription and phase II enzyme expression experimental_model: Reporter, expression and dominant-negative transcription-factor experiments limitations: Unidentified derivative extract was active; direct binding of intact lycopene to KEAP1 was not established. exposure: Lycopene and ethanolic derivative extract evidence_span: {"source_cache": "artifacts/lycopene-research/15657364.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "a25b93d6074a1e560bf1e163aa70c511e99199b9bb62ccdffdbe70e51fcc7c32", "start_char": 0, "end_char": 1890, "text_sha256": "a25b93d6074a1e560bf1e163aa70c511e99199b9bb62ccdffdbe70e51fcc7c32"} [lycopene-p15657364] Carotenoids activate the antioxidant response element transcription system. (2005). https://pubmed.ncbi.nlm.nih.gov/15657364/ DOI: 10.1158/1535-7163.177.4.1
Complete structured claim and evidenceApo-6-, 8-, 10-, 12- and 14-prime lycopenals were detected in foods and human plasma; the plasma sum was 1.9 nmol/L.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/20178389.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "eddfd89ee638c7e574f322fcba2dd9b82b006f235f98a845962fe12b47d0987d", "start_char": 0, "end_char": 1451, "text_sha256": "eddfd89ee638c7e574f322fcba2dd9b82b006f235f98a845962fe12b47d0987d"}
- experimental_model
- HPLC-MS/MS measurement of food and human plasma metabolites
- exposure
- Tomato juice for eight weeks; chemically prepared analytical standards
- limitations
- Detection cannot separate absorbed food metabolites from enzymatic or nonenzymatic formation in the body.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human plasma and foods
- plain_language
- Finding a breakdown product in blood does not tell us where it was made.
- primary_references
- [lycopene-p20178389] Identification and quantification of apo-lycopenals in fruits, vegetables, and human plasma. (2010). https://pubmed.ncbi.nlm.nih.gov/20178389/ DOI: 10.1021/jf100415z
- tissue_or_cell_type
- Plasma after tomato juice consumption; food extracts
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 403–414
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · HPLC-MS/MS measurement of food and human plasma metabolites · source_derived_draft · unverified_draft
### lycopene-plasma-apo-detection Apo-6-, 8-, 10-, 12- and 14-prime lycopenals were detected in foods and human plasma; the plasma sum was 1.9 nmol/L. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: Finding a breakdown product in blood does not tell us where it was made. organism: Human plasma and foods tissue_or_cell_type: Plasma after tomato juice consumption; food extracts experimental_model: HPLC-MS/MS measurement of food and human plasma metabolites limitations: Detection cannot separate absorbed food metabolites from enzymatic or nonenzymatic formation in the body. exposure: Tomato juice for eight weeks; chemically prepared analytical standards evidence_span: {"source_cache": "artifacts/lycopene-research/20178389.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "eddfd89ee638c7e574f322fcba2dd9b82b006f235f98a845962fe12b47d0987d", "start_char": 0, "end_char": 1451, "text_sha256": "eddfd89ee638c7e574f322fcba2dd9b82b006f235f98a845962fe12b47d0987d"} [lycopene-p20178389] Identification and quantification of apo-lycopenals in fruits, vegetables, and human plasma. (2010). https://pubmed.ncbi.nlm.nih.gov/20178389/ DOI: 10.1021/jf100415z
Complete structured claim and evidencePlasma malondialdehyde did not change significantly with lycopene.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/21430075.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "c1351b40c0701ce0b8e35bc9346b63650fbd2ee3a9263091aa6b304b9860a5e3", "start_char": 0, "end_char": 1314, "text_sha256": "c1351b40c0701ce0b8e35bc9346b63650fbd2ee3a9263091aa6b304b9860a5e3"}
- experimental_model
- Double-blind placebo-controlled prebiopsy trial
- exposure
- 30 mg/day tomato-oleoresin lycopene for 21 days
- limitations
- Short exposure; tissue and oxidation biomarkers do not establish cancer prevention or clinical benefit.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human, 105 African American male veterans
- plain_language
- A lipid-oxidation marker was also unchanged.
- primary_references
- [lycopene-p21430075] Antioxidant effects of lycopene in African American men with prostate cancer or benign prostate hyperplasia: a randomized, controlled trial. (2011). https://pubmed.ncbi.nlm.nih.gov/21430075/ DOI: 10.1158/1940-6207.capr-10-0288
- tissue_or_cell_type
- Plasma and prostate biopsy
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 1105–1116
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Double-blind placebo-controlled prebiopsy trial · source_derived_draft · unverified_draft
### lycopene-plasma-lipid-oxidation-null Plasma malondialdehyde did not change significantly with lycopene. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: A lipid-oxidation marker was also unchanged. organism: Human, 105 African American male veterans tissue_or_cell_type: Plasma and prostate biopsy experimental_model: Double-blind placebo-controlled prebiopsy trial limitations: Short exposure; tissue and oxidation biomarkers do not establish cancer prevention or clinical benefit. exposure: 30 mg/day tomato-oleoresin lycopene for 21 days evidence_span: {"source_cache": "artifacts/lycopene-research/21430075.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "c1351b40c0701ce0b8e35bc9346b63650fbd2ee3a9263091aa6b304b9860a5e3", "start_char": 0, "end_char": 1314, "text_sha256": "c1351b40c0701ce0b8e35bc9346b63650fbd2ee3a9263091aa6b304b9860a5e3"} [lycopene-p21430075] Antioxidant effects of lycopene in African American men with prostate cancer or benign prostate hyperplasia: a randomized, controlled trial. (2011). https://pubmed.ncbi.nlm.nih.gov/21430075/ DOI: 10.1158/1940-6207.capr-10-0288
Complete structured claim and evidenceSupplementation increased prostate lycopene from 0.45 to 0.59 pmol/mg and plasma lycopene from 0.74 to 1.43 micromolar.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/21430075.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "c1351b40c0701ce0b8e35bc9346b63650fbd2ee3a9263091aa6b304b9860a5e3", "start_char": 0, "end_char": 1314, "text_sha256": "c1351b40c0701ce0b8e35bc9346b63650fbd2ee3a9263091aa6b304b9860a5e3"}
- experimental_model
- Double-blind placebo-controlled prebiopsy trial
- exposure
- 30 mg/day tomato-oleoresin lycopene for 21 days
- limitations
- Short exposure; tissue and oxidation biomarkers do not establish cancer prevention or clinical benefit.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human, 105 African American male veterans
- plain_language
- The substance reached the tissue; delivery alone does not prove benefit.
- primary_references
- [lycopene-p21430075] Antioxidant effects of lycopene in African American men with prostate cancer or benign prostate hyperplasia: a randomized, controlled trial. (2011). https://pubmed.ncbi.nlm.nih.gov/21430075/ DOI: 10.1158/1940-6207.capr-10-0288
- tissue_or_cell_type
- Plasma and prostate biopsy
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 1079–1090
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Double-blind placebo-controlled prebiopsy trial · source_derived_draft · unverified_draft
### lycopene-prostate-delivery Supplementation increased prostate lycopene from 0.45 to 0.59 pmol/mg and plasma lycopene from 0.74 to 1.43 micromolar. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: The substance reached the tissue; delivery alone does not prove benefit. organism: Human, 105 African American male veterans tissue_or_cell_type: Plasma and prostate biopsy experimental_model: Double-blind placebo-controlled prebiopsy trial limitations: Short exposure; tissue and oxidation biomarkers do not establish cancer prevention or clinical benefit. exposure: 30 mg/day tomato-oleoresin lycopene for 21 days evidence_span: {"source_cache": "artifacts/lycopene-research/21430075.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "c1351b40c0701ce0b8e35bc9346b63650fbd2ee3a9263091aa6b304b9860a5e3", "start_char": 0, "end_char": 1314, "text_sha256": "c1351b40c0701ce0b8e35bc9346b63650fbd2ee3a9263091aa6b304b9860a5e3"} [lycopene-p21430075] Antioxidant effects of lycopene in African American men with prostate cancer or benign prostate hyperplasia: a randomized, controlled trial. (2011). https://pubmed.ncbi.nlm.nih.gov/21430075/ DOI: 10.1158/1940-6207.capr-10-0288
Complete structured claim and evidenceNo significant reduction in prostate 8-oxo-deoxyguanosine followed lycopene treatment.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/21430075.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "c1351b40c0701ce0b8e35bc9346b63650fbd2ee3a9263091aa6b304b9860a5e3", "start_char": 0, "end_char": 1314, "text_sha256": "c1351b40c0701ce0b8e35bc9346b63650fbd2ee3a9263091aa6b304b9860a5e3"}
- experimental_model
- Double-blind placebo-controlled prebiopsy trial
- exposure
- 30 mg/day tomato-oleoresin lycopene for 21 days
- limitations
- Short exposure; tissue and oxidation biomarkers do not establish cancer prevention or clinical benefit.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human, 105 African American male veterans
- plain_language
- A DNA-oxidation marker did not improve despite increased exposure.
- primary_references
- [lycopene-p21430075] Antioxidant effects of lycopene in African American men with prostate cancer or benign prostate hyperplasia: a randomized, controlled trial. (2011). https://pubmed.ncbi.nlm.nih.gov/21430075/ DOI: 10.1158/1940-6207.capr-10-0288
- tissue_or_cell_type
- Plasma and prostate biopsy
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 1092–1103
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Double-blind placebo-controlled prebiopsy trial · source_derived_draft · unverified_draft
### lycopene-prostate-dna-oxidation-null No significant reduction in prostate 8-oxo-deoxyguanosine followed lycopene treatment. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: A DNA-oxidation marker did not improve despite increased exposure. organism: Human, 105 African American male veterans tissue_or_cell_type: Plasma and prostate biopsy experimental_model: Double-blind placebo-controlled prebiopsy trial limitations: Short exposure; tissue and oxidation biomarkers do not establish cancer prevention or clinical benefit. exposure: 30 mg/day tomato-oleoresin lycopene for 21 days evidence_span: {"source_cache": "artifacts/lycopene-research/21430075.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "c1351b40c0701ce0b8e35bc9346b63650fbd2ee3a9263091aa6b304b9860a5e3", "start_char": 0, "end_char": 1314, "text_sha256": "c1351b40c0701ce0b8e35bc9346b63650fbd2ee3a9263091aa6b304b9860a5e3"} [lycopene-p21430075] Antioxidant effects of lycopene in African American men with prostate cancer or benign prostate hyperplasia: a randomized, controlled trial. (2011). https://pubmed.ncbi.nlm.nih.gov/21430075/ DOI: 10.1158/1940-6207.capr-10-0288
Complete structured claim and evidenceLycopene quenched singlet oxygen faster per molecule than alpha-tocopherol, but concentration-adjusted plasma capacities were comparable.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/2802626.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "91ad9c300da17ee4e4c78a9ba980a7a4f05eef2328a64b5a9f75d4023abdc521", "start_char": 0, "end_char": 1046, "text_sha256": "91ad9c300da17ee4e4c78a9ba980a7a4f05eef2328a64b5a9f75d4023abdc521"}
- experimental_model
- Cell-free singlet-oxygen quenching comparison
- exposure
- Lycopene, beta-carotene, alpha-tocopherol and albumin-bound bilirubin
- limitations
- Rate constants are solvent/assay-dependent, not a clinical ranking of antioxidant supplements.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Chemical assay and plasma-concentration comparison
- plain_language
- A faster molecule is not automatically the more important antioxidant in blood.
- primary_references
- [lycopene-p2802626] Lycopene as the most efficient biological carotenoid singlet oxygen quencher. (1989). https://pubmed.ncbi.nlm.nih.gov/2802626/ DOI: 10.1016/0003-9861(89)90467-0
- tissue_or_cell_type
- Solution kinetics
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 429–440
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Cell-free singlet-oxygen quenching comparison · source_derived_draft · unverified_draft
### lycopene-quenching-comparison Lycopene quenched singlet oxygen faster per molecule than alpha-tocopherol, but concentration-adjusted plasma capacities were comparable. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: A faster molecule is not automatically the more important antioxidant in blood. organism: Chemical assay and plasma-concentration comparison tissue_or_cell_type: Solution kinetics experimental_model: Cell-free singlet-oxygen quenching comparison limitations: Rate constants are solvent/assay-dependent, not a clinical ranking of antioxidant supplements. exposure: Lycopene, beta-carotene, alpha-tocopherol and albumin-bound bilirubin evidence_span: {"source_cache": "artifacts/lycopene-research/2802626.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "91ad9c300da17ee4e4c78a9ba980a7a4f05eef2328a64b5a9f75d4023abdc521", "start_char": 0, "end_char": 1046, "text_sha256": "91ad9c300da17ee4e4c78a9ba980a7a4f05eef2328a64b5a9f75d4023abdc521"} [lycopene-p2802626] Lycopene as the most efficient biological carotenoid singlet oxygen quencher. (1989). https://pubmed.ncbi.nlm.nih.gov/2802626/ DOI: 10.1016/0003-9861(89)90467-0
Complete structured claim and evidenceLycopene downregulated 5-alpha-reductase expression in the rat prostate tumor model.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/15084515.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "682a0c4c6a001993efa3bada4aa3d381723feb78b410fd703b8de72517eef62c", "start_char": 0, "end_char": 1410, "text_sha256": "682a0c4c6a001993efa3bada4aa3d381723feb78b410fd703b8de72517eef62c"}
- experimental_model
- Dietary intervention and tumor gene-expression analysis
- exposure
- 200 ppm lycopene, 540 ppm vitamin E or both for four weeks
- limitations
- Preclinical gene-expression findings; not established human steroid suppression or cancer treatment.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Rat MatLyLu Dunning prostate tumor model
- plain_language
- A testosterone-activation pathway changed in this animal tumor setting.
- primary_references
- [lycopene-p15084515] Lycopene and vitamin E interfere with autocrine/paracrine loops in the Dunning prostate cancer model. (2004). https://pubmed.ncbi.nlm.nih.gov/15084515/ DOI: 10.1096/fj.03-1116fje
- tissue_or_cell_type
- Tumor tissue
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 897–908
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Dietary intervention and tumor gene-expression analysis · source_derived_draft · unverified_draft
### lycopene-rat-5alpha Lycopene downregulated 5-alpha-reductase expression in the rat prostate tumor model. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: A testosterone-activation pathway changed in this animal tumor setting. organism: Rat MatLyLu Dunning prostate tumor model tissue_or_cell_type: Tumor tissue experimental_model: Dietary intervention and tumor gene-expression analysis limitations: Preclinical gene-expression findings; not established human steroid suppression or cancer treatment. exposure: 200 ppm lycopene, 540 ppm vitamin E or both for four weeks evidence_span: {"source_cache": "artifacts/lycopene-research/15084515.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "682a0c4c6a001993efa3bada4aa3d381723feb78b410fd703b8de72517eef62c", "start_char": 0, "end_char": 1410, "text_sha256": "682a0c4c6a001993efa3bada4aa3d381723feb78b410fd703b8de72517eef62c"} [lycopene-p15084515] Lycopene and vitamin E interfere with autocrine/paracrine loops in the Dunning prostate cancer model. (2004). https://pubmed.ncbi.nlm.nih.gov/15084515/ DOI: 10.1096/fj.03-1116fje
Complete structured claim and evidenceLycopene downregulated local IGF-I expression in the rat tumor experiment.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/15084515.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "682a0c4c6a001993efa3bada4aa3d381723feb78b410fd703b8de72517eef62c", "start_char": 0, "end_char": 1410, "text_sha256": "682a0c4c6a001993efa3bada4aa3d381723feb78b410fd703b8de72517eef62c"}
- experimental_model
- Dietary intervention and tumor gene-expression analysis
- exposure
- 200 ppm lycopene, 540 ppm vitamin E or both for four weeks
- limitations
- Preclinical gene-expression findings; not established human steroid suppression or cancer treatment.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Rat MatLyLu Dunning prostate tumor model
- plain_language
- This was local tumor signaling, not measured human blood IGF-I.
- primary_references
- [lycopene-p15084515] Lycopene and vitamin E interfere with autocrine/paracrine loops in the Dunning prostate cancer model. (2004). https://pubmed.ncbi.nlm.nih.gov/15084515/ DOI: 10.1096/fj.03-1116fje
- tissue_or_cell_type
- Tumor tissue
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 910–921
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Dietary intervention and tumor gene-expression analysis · source_derived_draft · unverified_draft
### lycopene-rat-igf Lycopene downregulated local IGF-I expression in the rat tumor experiment. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: This was local tumor signaling, not measured human blood IGF-I. organism: Rat MatLyLu Dunning prostate tumor model tissue_or_cell_type: Tumor tissue experimental_model: Dietary intervention and tumor gene-expression analysis limitations: Preclinical gene-expression findings; not established human steroid suppression or cancer treatment. exposure: 200 ppm lycopene, 540 ppm vitamin E or both for four weeks evidence_span: {"source_cache": "artifacts/lycopene-research/15084515.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "682a0c4c6a001993efa3bada4aa3d381723feb78b410fd703b8de72517eef62c", "start_char": 0, "end_char": 1410, "text_sha256": "682a0c4c6a001993efa3bada4aa3d381723feb78b410fd703b8de72517eef62c"} [lycopene-p15084515] Lycopene and vitamin E interfere with autocrine/paracrine loops in the Dunning prostate cancer model. (2004). https://pubmed.ncbi.nlm.nih.gov/15084515/ DOI: 10.1096/fj.03-1116fje
Complete structured claim and evidenceLycopene downregulated local IL-6 expression in the rat tumor experiment.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/15084515.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "682a0c4c6a001993efa3bada4aa3d381723feb78b410fd703b8de72517eef62c", "start_char": 0, "end_char": 1410, "text_sha256": "682a0c4c6a001993efa3bada4aa3d381723feb78b410fd703b8de72517eef62c"}
- experimental_model
- Dietary intervention and tumor gene-expression analysis
- exposure
- 200 ppm lycopene, 540 ppm vitamin E or both for four weeks
- limitations
- Preclinical gene-expression findings; not established human steroid suppression or cancer treatment.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Rat MatLyLu Dunning prostate tumor model
- plain_language
- An inflammatory signaling measurement also changed.
- primary_references
- [lycopene-p15084515] Lycopene and vitamin E interfere with autocrine/paracrine loops in the Dunning prostate cancer model. (2004). https://pubmed.ncbi.nlm.nih.gov/15084515/ DOI: 10.1096/fj.03-1116fje
- tissue_or_cell_type
- Tumor tissue
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 923–934
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Dietary intervention and tumor gene-expression analysis · source_derived_draft · unverified_draft
### lycopene-rat-il6 Lycopene downregulated local IL-6 expression in the rat tumor experiment. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: An inflammatory signaling measurement also changed. organism: Rat MatLyLu Dunning prostate tumor model tissue_or_cell_type: Tumor tissue experimental_model: Dietary intervention and tumor gene-expression analysis limitations: Preclinical gene-expression findings; not established human steroid suppression or cancer treatment. exposure: 200 ppm lycopene, 540 ppm vitamin E or both for four weeks evidence_span: {"source_cache": "artifacts/lycopene-research/15084515.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "682a0c4c6a001993efa3bada4aa3d381723feb78b410fd703b8de72517eef62c", "start_char": 0, "end_char": 1410, "text_sha256": "682a0c4c6a001993efa3bada4aa3d381723feb78b410fd703b8de72517eef62c"} [lycopene-p15084515] Lycopene and vitamin E interfere with autocrine/paracrine loops in the Dunning prostate cancer model. (2004). https://pubmed.ncbi.nlm.nih.gov/15084515/ DOI: 10.1096/fj.03-1116fje
Complete structured claim and evidenceLycopene had a reported singlet-oxygen quenching constant of 31 billion per molar per second in the assay.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/2802626.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "91ad9c300da17ee4e4c78a9ba980a7a4f05eef2328a64b5a9f75d4023abdc521", "start_char": 0, "end_char": 1046, "text_sha256": "91ad9c300da17ee4e4c78a9ba980a7a4f05eef2328a64b5a9f75d4023abdc521"}
- experimental_model
- Cell-free singlet-oxygen quenching comparison
- exposure
- Lycopene, beta-carotene, alpha-tocopherol and albumin-bound bilirubin
- limitations
- Rate constants are solvent/assay-dependent, not a clinical ranking of antioxidant supplements.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Chemical assay and plasma-concentration comparison
- plain_language
- It can remove excitation energy from this reactive oxygen species.
- primary_references
- [lycopene-p2802626] Lycopene as the most efficient biological carotenoid singlet oxygen quencher. (1989). https://pubmed.ncbi.nlm.nih.gov/2802626/ DOI: 10.1016/0003-9861(89)90467-0
- tissue_or_cell_type
- Solution kinetics
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 416–427
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Cell-free singlet-oxygen quenching comparison · source_derived_draft · unverified_draft
### lycopene-singlet-quenching Lycopene had a reported singlet-oxygen quenching constant of 31 billion per molar per second in the assay. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: It can remove excitation energy from this reactive oxygen species. organism: Chemical assay and plasma-concentration comparison tissue_or_cell_type: Solution kinetics experimental_model: Cell-free singlet-oxygen quenching comparison limitations: Rate constants are solvent/assay-dependent, not a clinical ranking of antioxidant supplements. exposure: Lycopene, beta-carotene, alpha-tocopherol and albumin-bound bilirubin evidence_span: {"source_cache": "artifacts/lycopene-research/2802626.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "91ad9c300da17ee4e4c78a9ba980a7a4f05eef2328a64b5a9f75d4023abdc521", "start_char": 0, "end_char": 1046, "text_sha256": "91ad9c300da17ee4e4c78a9ba980a7a4f05eef2328a64b5a9f75d4023abdc521"} [lycopene-p2802626] Lycopene as the most efficient biological carotenoid singlet oxygen quencher. (1989). https://pubmed.ncbi.nlm.nih.gov/2802626/ DOI: 10.1016/0003-9861(89)90467-0
Complete structured claim and evidenceNeither capsule nor paste showed improvement in visual minimal erythema dose over the ten-week UVB study.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/26024575.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "682051a8b59270407b327cf439145fec1ea55459fd3c6e8236b535f985442d00", "start_char": 0, "end_char": 1667, "text_sha256": "682051a8b59270407b327cf439145fec1ea55459fd3c6e8236b535f985442d00"}
- experimental_model
- Randomized comparative capsule-versus-paste study
- exposure
- Ten weeks of capsule or tomato paste
- limitations
- Small study without an untreated placebo group; differs in UV spectrum and outcomes from the 2011 study.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human, 20 enrolled; three withdrew after week four
- plain_language
- Skin protection was not a consistent result across protocols.
- primary_references
- [lycopene-p26024575] Lycopene not in pill, nor in natura has photoprotective systemic effect. (2015). https://pubmed.ncbi.nlm.nih.gov/26024575/ DOI: 10.1007/s00403-015-1578-7
- tissue_or_cell_type
- UVB-induced erythema and serum lycopene
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 1235–1246
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Randomized comparative capsule-versus-paste study · source_derived_draft · unverified_draft
### lycopene-skin-replication-null Neither capsule nor paste showed improvement in visual minimal erythema dose over the ten-week UVB study. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: Skin protection was not a consistent result across protocols. organism: Human, 20 enrolled; three withdrew after week four tissue_or_cell_type: UVB-induced erythema and serum lycopene experimental_model: Randomized comparative capsule-versus-paste study limitations: Small study without an untreated placebo group; differs in UV spectrum and outcomes from the 2011 study. exposure: Ten weeks of capsule or tomato paste evidence_span: {"source_cache": "artifacts/lycopene-research/26024575.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "682051a8b59270407b327cf439145fec1ea55459fd3c6e8236b535f985442d00", "start_char": 0, "end_char": 1667, "text_sha256": "682051a8b59270407b327cf439145fec1ea55459fd3c6e8236b535f985442d00"} [lycopene-p26024575] Lycopene not in pill, nor in natura has photoprotective systemic effect. (2015). https://pubmed.ncbi.nlm.nih.gov/26024575/ DOI: 10.1007/s00403-015-1578-7
Complete structured claim and evidenceThe trial reported improved total sperm count, remaining significant after adjustment.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/31468596.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "43f86ccba4712a72d13292bf7fea87e9feb0c514ff5bebcd79adf94f656522c4", "start_char": 0, "end_char": 1442, "text_sha256": "43f86ccba4712a72d13292bf7fea87e9feb0c514ff5bebcd79adf94f656522c4"}
- experimental_model
- Double-blind placebo-controlled trial
- exposure
- 25 mg/day lycopene for 12 weeks
- limitations
- Small trial; distinguish between-group adjusted results from numerous within-group changes; no live-birth outcome established.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human, 44 men with oligozoospermia
- plain_language
- A semen measurement improved; this does not establish better pregnancy or live-birth rates.
- primary_references
- [lycopene-p31468596] The effects of lycopene supplement on the spermatogram and seminal oxidative stress in infertile men: A randomized, double-blind, placebo-controlled clinical trial. (2019). https://pubmed.ncbi.nlm.nih.gov/31468596/ DOI: 10.1002/ptr.6493
- tissue_or_cell_type
- Semen analysis
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 1248–1259
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Double-blind placebo-controlled trial · source_derived_draft · unverified_draft
### lycopene-sperm-count The trial reported improved total sperm count, remaining significant after adjustment. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: A semen measurement improved; this does not establish better pregnancy or live-birth rates. organism: Human, 44 men with oligozoospermia tissue_or_cell_type: Semen analysis experimental_model: Double-blind placebo-controlled trial limitations: Small trial; distinguish between-group adjusted results from numerous within-group changes; no live-birth outcome established. exposure: 25 mg/day lycopene for 12 weeks evidence_span: {"source_cache": "artifacts/lycopene-research/31468596.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "43f86ccba4712a72d13292bf7fea87e9feb0c514ff5bebcd79adf94f656522c4", "start_char": 0, "end_char": 1442, "text_sha256": "43f86ccba4712a72d13292bf7fea87e9feb0c514ff5bebcd79adf94f656522c4"} [lycopene-p31468596] The effects of lycopene supplement on the spermatogram and seminal oxidative stress in infertile men: A randomized, double-blind, placebo-controlled clinical trial. (2019). https://pubmed.ncbi.nlm.nih.gov/31468596/ DOI: 10.1002/ptr.6493
Complete structured claim and evidenceMean fractional lycopene absorption was 23% ± 6% in the human carbon-13 tracer experiment.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/26561629.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "fdc01c055cd2de5fc7523b3a3f4486ea939d5d197aaf214000328194f9586682", "start_char": 0, "end_char": 2207, "text_sha256": "fdc01c055cd2de5fc7523b3a3f4486ea939d5d197aaf214000328194f9586682"}
- experimental_model
- Stable-isotope tracer and seven-compartment kinetic modeling
- exposure
- 10.2 mg carbon-13 lycopene, 82% all-trans and 18% cis
- limitations
- Small study; model-dependent pool estimates; formulation differs from food-matrix comparisons.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human, eight healthy adults
- plain_language
- Only part of an oral dose reached the body in this study.
- primary_references
- [lycopene-p26561629] Compartmental and noncompartmental modeling of ¹³C-lycopene absorption, isomerization, and distribution kinetics in healthy adults. (2015). https://pubmed.ncbi.nlm.nih.gov/26561629/ DOI: 10.3945/ajcn.114.103143
- tissue_or_cell_type
- Plasma over 28 days and modeled tissue pools
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 195–206
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Stable-isotope tracer and seven-compartment kinetic modeling · source_derived_draft · unverified_draft
### lycopene-tracer-absorption Mean fractional lycopene absorption was 23% ± 6% in the human carbon-13 tracer experiment. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: Only part of an oral dose reached the body in this study. organism: Human, eight healthy adults tissue_or_cell_type: Plasma over 28 days and modeled tissue pools experimental_model: Stable-isotope tracer and seven-compartment kinetic modeling limitations: Small study; model-dependent pool estimates; formulation differs from food-matrix comparisons. exposure: 10.2 mg carbon-13 lycopene, 82% all-trans and 18% cis evidence_span: {"source_cache": "artifacts/lycopene-research/26561629.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "fdc01c055cd2de5fc7523b3a3f4486ea939d5d197aaf214000328194f9586682", "start_char": 0, "end_char": 2207, "text_sha256": "fdc01c055cd2de5fc7523b3a3f4486ea939d5d197aaf214000328194f9586682"} [lycopene-p26561629] Compartmental and noncompartmental modeling of ¹³C-lycopene absorption, isomerization, and distribution kinetics in healthy adults. (2015). https://pubmed.ncbi.nlm.nih.gov/26561629/ DOI: 10.3945/ajcn.114.103143
Complete structured claim and evidenceLycopene did not significantly reduce lutein uptake in the same mixed-micelle assay.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lutein-research/15554873.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "3dfbef37e3c73db4732f66083063e548a1654cb759ff46392c981c50f338d8a0", "start_char": 0, "end_char": 2014, "text_sha256": "3dfbef37e3c73db4732f66083063e548a1654cb759ff46392c981c50f338d8a0"}
- experimental_model
- Mixed-micelle transport across Caco-2 TC-7 monolayers
- exposure
- Micellar lutein 1.5–15 micromolar; antibodies and BLT1
- limitations
- Partial inhibition supports a contribution, not an exclusive route; cell experiments do not set clinical supplement spacing.
- nutrient_topic
- Lutein research collection; topical membership is not evidence of a direct dietary effect. · Lutein
- organism
- Human intestinal cell model
- plain_language
- Shared transport does not mean every pair competes equally.
- primary_references
- [lutein-p15554873] Lutein transport by Caco-2 TC-7 cells occurs partly by a facilitated process involving the scavenger receptor class B type I (SR-BI). (2005). https://pubmed.ncbi.nlm.nih.gov/15554873/ DOI: 10.1042/bj20040554
- tissue_or_cell_type
- Apical intestinal epithelial transport
Lutein: metabolism, signaling and nutrient connections (2026-09-17) · lines 502–513
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Mixed-micelle transport across Caco-2 TC-7 monolayers · source_derived_draft · unverified_draft
### lutein-lycopene-null Lycopene did not significantly reduce lutein uptake in the same mixed-micelle assay. Condition category: normal nutrient_topic: Lutein research collection; topical membership is not evidence of a direct dietary effect. plain_language: Shared transport does not mean every pair competes equally. organism: Human intestinal cell model tissue_or_cell_type: Apical intestinal epithelial transport experimental_model: Mixed-micelle transport across Caco-2 TC-7 monolayers limitations: Partial inhibition supports a contribution, not an exclusive route; cell experiments do not set clinical supplement spacing. exposure: Micellar lutein 1.5–15 micromolar; antibodies and BLT1 evidence_span: {"source_cache": "artifacts/lutein-research/15554873.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "3dfbef37e3c73db4732f66083063e548a1654cb759ff46392c981c50f338d8a0", "start_char": 0, "end_char": 2014, "text_sha256": "3dfbef37e3c73db4732f66083063e548a1654cb759ff46392c981c50f338d8a0"} [lutein-p15554873] Lutein transport by Caco-2 TC-7 cells occurs partly by a facilitated process involving the scavenger receptor class B type I (SR-BI). (2005). https://pubmed.ncbi.nlm.nih.gov/15554873/ DOI: 10.1042/bj20040554
Complete structured claim and evidence
What acts on it
SR-BI antibody or BLT1 inhibited all-E and 5Z lycopene uptake by up to 60% in Caco-2 monolayers.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/18641187.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "7c71fd4fd3be9d14176bceb3c2104143269a788587feec232350a6f1c5913e3d", "start_char": 0, "end_char": 1557, "text_sha256": "7c71fd4fd3be9d14176bceb3c2104143269a788587feec232350a6f1c5913e3d"}
- experimental_model
- Transporter inhibition in Caco-2 cells; intestinal SR-BI transgenic mice
- exposure
- All-E and 5Z lycopene; mice received 0.25 g/kg diet for one month
- limitations
- Partial uptake inhibition is not proof of a sole transporter. Ezetimibe result is a cell assay, not a clinical drug-interaction trial.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human Caco-2 cells
- plain_language
- One intestinal lipid transporter helps lycopene enter these cells.
- primary_references
- [lycopene-p18641187] Lycopene absorption in human intestinal cells and in mice involves scavenger receptor class B type I but not Niemann-Pick C1-like 1. (2008). https://pubmed.ncbi.nlm.nih.gov/18641187/ DOI: 10.1093/jn/138.8.1432
- tissue_or_cell_type
- Intestinal epithelium and plasma
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 104–115
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Transporter inhibition in Caco-2 cells; intestinal SR-BI transgenic mice · source_derived_draft · unverified_draft
### lycopene-srbi-uptake SR-BI antibody or BLT1 inhibited all-E and 5Z lycopene uptake by up to 60% in Caco-2 monolayers. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: One intestinal lipid transporter helps lycopene enter these cells. organism: Human Caco-2 cells tissue_or_cell_type: Intestinal epithelium and plasma experimental_model: Transporter inhibition in Caco-2 cells; intestinal SR-BI transgenic mice limitations: Partial uptake inhibition is not proof of a sole transporter. Ezetimibe result is a cell assay, not a clinical drug-interaction trial. exposure: All-E and 5Z lycopene; mice received 0.25 g/kg diet for one month evidence_span: {"source_cache": "artifacts/lycopene-research/18641187.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "7c71fd4fd3be9d14176bceb3c2104143269a788587feec232350a6f1c5913e3d", "start_char": 0, "end_char": 1557, "text_sha256": "7c71fd4fd3be9d14176bceb3c2104143269a788587feec232350a6f1c5913e3d"} [lycopene-p18641187] Lycopene absorption in human intestinal cells and in mice involves scavenger receptor class B type I but not Niemann-Pick C1-like 1. (2008). https://pubmed.ncbi.nlm.nih.gov/18641187/ DOI: 10.1093/jn/138.8.1432
Complete structured claim and evidence
Where it participates (unsigned role)
Adding avocado to salsa increased mean lycopene TRL AUC 4.4-fold compared with avocado-free salsa.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/15735074.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "31bfa6900bd41221e84a0713fc5ccf97341dfb80d997eecc37a1f2a121b9d814", "start_char": 0, "end_char": 1730, "text_sha256": "31bfa6900bd41221e84a0713fc5ccf97341dfb80d997eecc37a1f2a121b9d814"}
- experimental_model
- Acute crossover meal experiment
- exposure
- Salsa with or without 150 g avocado; 9.5-hour sampling
- limitations
- Food comparison, not a requirement for this quantity of fat or evidence of a specific fatty-acid cofactor.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human, 11 participants in the salsa study
- plain_language
- Eating the carotenoid within a meal containing fat changed absorption.
- primary_references
- [lycopene-p15735074] Carotenoid absorption from salad and salsa by humans is enhanced by the addition of avocado or avocado oil. (2005). https://pubmed.ncbi.nlm.nih.gov/15735074/ DOI: 10.1093/jn/135.3.431
- tissue_or_cell_type
- Postprandial triglyceride-rich lipoproteins
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 767–778
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Acute crossover meal experiment · source_derived_draft · unverified_draft
### lycopene-avocado-absorption Adding avocado to salsa increased mean lycopene TRL AUC 4.4-fold compared with avocado-free salsa. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: Eating the carotenoid within a meal containing fat changed absorption. organism: Human, 11 participants in the salsa study tissue_or_cell_type: Postprandial triglyceride-rich lipoproteins experimental_model: Acute crossover meal experiment limitations: Food comparison, not a requirement for this quantity of fat or evidence of a specific fatty-acid cofactor. exposure: Salsa with or without 150 g avocado; 9.5-hour sampling evidence_span: {"source_cache": "artifacts/lycopene-research/15735074.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "31bfa6900bd41221e84a0713fc5ccf97341dfb80d997eecc37a1f2a121b9d814", "start_char": 0, "end_char": 1730, "text_sha256": "31bfa6900bd41221e84a0713fc5ccf97341dfb80d997eecc37a1f2a121b9d814"} [lycopene-p15735074] Carotenoid absorption from salad and salsa by humans is enhanced by the addition of avocado or avocado oil. (2005). https://pubmed.ncbi.nlm.nih.gov/15735074/ DOI: 10.1093/jn/135.3.431
Complete structured claim and evidencePurified recombinant human BCO1 generated acycloretinal from lycopene, with reported catalytic efficiency similar to beta-carotene.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/24187135.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "cf8ce69a4772c58e274590a2e3f251bed46de77b4d844b54c98d39fcd27e3e91", "start_char": 0, "end_char": 1772, "text_sha256": "cf8ce69a4772c58e274590a2e3f251bed46de77b4d844b54c98d39fcd27e3e91"}
- experimental_model
- Purified recombinant human enzyme kinetics
- exposure
- Substrate panel; product chromatography
- limitations
- Activity in a purified enzyme system does not establish dominant in-vivo flux; acycloretinal is not retinal or vitamin A.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human BCO1 expressed in E. coli
- plain_language
- This product lacks the ring of vitamin-A retinal; cleavage does not make lycopene a vitamin A source.
- primary_references
- [lycopene-p24187135] Substrate specificity of purified recombinant human β-carotene 15,15'-oxygenase (BCO1). (2013). https://pubmed.ncbi.nlm.nih.gov/24187135/ DOI: 10.1074/jbc.m113.507160
- tissue_or_cell_type
- Cell-free carotenoid cleavage
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 377–388
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Purified recombinant human enzyme kinetics · source_derived_draft · unverified_draft
### lycopene-bco1-acycloretinal Purified recombinant human BCO1 generated acycloretinal from lycopene, with reported catalytic efficiency similar to beta-carotene. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: This product lacks the ring of vitamin-A retinal; cleavage does not make lycopene a vitamin A source. organism: Human BCO1 expressed in E. coli tissue_or_cell_type: Cell-free carotenoid cleavage experimental_model: Purified recombinant human enzyme kinetics limitations: Activity in a purified enzyme system does not establish dominant in-vivo flux; acycloretinal is not retinal or vitamin A. exposure: Substrate panel; product chromatography evidence_span: {"source_cache": "artifacts/lycopene-research/24187135.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "cf8ce69a4772c58e274590a2e3f251bed46de77b4d844b54c98d39fcd27e3e91", "start_char": 0, "end_char": 1772, "text_sha256": "cf8ce69a4772c58e274590a2e3f251bed46de77b4d844b54c98d39fcd27e3e91"} [lycopene-p24187135] Substrate specificity of purified recombinant human β-carotene 15,15'-oxygenase (BCO1). (2013). https://pubmed.ncbi.nlm.nih.gov/24187135/ DOI: 10.1074/jbc.m113.507160
Complete structured claim and evidenceCo-dosing beta-carotene increased the 24-hour lycopene AUC relative to lycopene alone.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/9278568.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "e318f6fef0bfed88403fa2adf46f9713ebddfe6ea586c29614e820442c57d056", "start_char": 0, "end_char": 1510, "text_sha256": "e318f6fef0bfed88403fa2adf46f9713ebddfe6ea586c29614e820442c57d056"}
- experimental_model
- Randomized-order double-blind crossover dosing experiment
- exposure
- 60 mg beta-carotene, 60 mg lycopene, or 60 mg of each together
- limitations
- Acute high-dose study; does not justify routine co-supplementation or establish universal competition rules.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human, ten healthy men
- plain_language
- Two carotenoids did not simply block one another in this experiment.
- primary_references
- [lycopene-p9278568] Ingestion by men of a combined dose of beta-carotene and lycopene does not affect the absorption of beta-carotene but improves that of lycopene. (1997). https://pubmed.ncbi.nlm.nih.gov/9278568/ DOI: 10.1093/jn/127.9.1833
- tissue_or_cell_type
- Serum carotenoid AUC over 24 hours
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 780–791
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Randomized-order double-blind crossover dosing experiment · source_derived_draft · unverified_draft
### lycopene-beta-carotene-co-dose Co-dosing beta-carotene increased the 24-hour lycopene AUC relative to lycopene alone. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: Two carotenoids did not simply block one another in this experiment. organism: Human, ten healthy men tissue_or_cell_type: Serum carotenoid AUC over 24 hours experimental_model: Randomized-order double-blind crossover dosing experiment limitations: Acute high-dose study; does not justify routine co-supplementation or establish universal competition rules. exposure: 60 mg beta-carotene, 60 mg lycopene, or 60 mg of each together evidence_span: {"source_cache": "artifacts/lycopene-research/9278568.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "e318f6fef0bfed88403fa2adf46f9713ebddfe6ea586c29614e820442c57d056", "start_char": 0, "end_char": 1510, "text_sha256": "e318f6fef0bfed88403fa2adf46f9713ebddfe6ea586c29614e820442c57d056"} [lycopene-p9278568] Ingestion by men of a combined dose of beta-carotene and lycopene does not affect the absorption of beta-carotene but improves that of lycopene. (1997). https://pubmed.ncbi.nlm.nih.gov/9278568/ DOI: 10.1093/jn/127.9.1833
Complete structured claim and evidenceCD36 inhibition or partial knockdown reduced lycopene uptake in 3T3-L1 adipocytes.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/21462325.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "de4990e5a9c520e6e528e181a4e81a469a4ebac313151bfa7828ad935b04a823", "start_char": 0, "end_char": 1048, "text_sha256": "de4990e5a9c520e6e528e181a4e81a469a4ebac313151bfa7828ad935b04a823"}
- experimental_model
- Transport inhibition, siRNA, overexpression and knockout explants
- exposure
- CD36 inhibitor, partial knockdown and Cd36-null tissue
- limitations
- Do not relabel adipose results as intestinal uptake or a clinical human transport-deficiency syndrome.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Mouse 3T3-L1 adipocytes and mouse adipose explants; COS-1 expression experiment
- plain_language
- Fat cells have uptake machinery for lycopene too.
- primary_references
- [lycopene-p21462325] CD36 is involved in lycopene and lutein uptake by adipocytes and adipose tissue cultures. (2011). https://pubmed.ncbi.nlm.nih.gov/21462325/ DOI: 10.1002/mnfr.201000399
- tissue_or_cell_type
- Adipocytes and adipose tissue
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 260–271
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Transport inhibition, siRNA, overexpression and knockout explants · source_derived_draft · unverified_draft
### lycopene-cd36-adipocyte CD36 inhibition or partial knockdown reduced lycopene uptake in 3T3-L1 adipocytes. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: Fat cells have uptake machinery for lycopene too. organism: Mouse 3T3-L1 adipocytes and mouse adipose explants; COS-1 expression experiment tissue_or_cell_type: Adipocytes and adipose tissue experimental_model: Transport inhibition, siRNA, overexpression and knockout explants limitations: Do not relabel adipose results as intestinal uptake or a clinical human transport-deficiency syndrome. exposure: CD36 inhibitor, partial knockdown and Cd36-null tissue evidence_span: {"source_cache": "artifacts/lycopene-research/21462325.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "de4990e5a9c520e6e528e181a4e81a469a4ebac313151bfa7828ad935b04a823", "start_char": 0, "end_char": 1048, "text_sha256": "de4990e5a9c520e6e528e181a4e81a469a4ebac313151bfa7828ad935b04a823"} [lycopene-p21462325] CD36 is involved in lycopene and lutein uptake by adipocytes and adipose tissue cultures. (2011). https://pubmed.ncbi.nlm.nih.gov/21462325/ DOI: 10.1002/mnfr.201000399
Complete structured claim and evidenceAdipose explants from Cd36-null mice took up less lycopene than wild-type explants.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/21462325.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "de4990e5a9c520e6e528e181a4e81a469a4ebac313151bfa7828ad935b04a823", "start_char": 0, "end_char": 1048, "text_sha256": "de4990e5a9c520e6e528e181a4e81a469a4ebac313151bfa7828ad935b04a823"}
- experimental_model
- Transport inhibition, siRNA, overexpression and knockout explants
- exposure
- CD36 inhibitor, partial knockdown and Cd36-null tissue
- limitations
- Do not relabel adipose results as intestinal uptake or a clinical human transport-deficiency syndrome.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Mouse 3T3-L1 adipocytes and mouse adipose explants; COS-1 expression experiment
- plain_language
- Removing this transporter reduced entry into mouse fat tissue.
- primary_references
- [lycopene-p21462325] CD36 is involved in lycopene and lutein uptake by adipocytes and adipose tissue cultures. (2011). https://pubmed.ncbi.nlm.nih.gov/21462325/ DOI: 10.1002/mnfr.201000399
- tissue_or_cell_type
- Adipocytes and adipose tissue
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 273–284
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Transport inhibition, siRNA, overexpression and knockout explants · source_derived_draft · unverified_draft
### lycopene-cd36-knockout Adipose explants from Cd36-null mice took up less lycopene than wild-type explants. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: Removing this transporter reduced entry into mouse fat tissue. organism: Mouse 3T3-L1 adipocytes and mouse adipose explants; COS-1 expression experiment tissue_or_cell_type: Adipocytes and adipose tissue experimental_model: Transport inhibition, siRNA, overexpression and knockout explants limitations: Do not relabel adipose results as intestinal uptake or a clinical human transport-deficiency syndrome. exposure: CD36 inhibitor, partial knockdown and Cd36-null tissue evidence_span: {"source_cache": "artifacts/lycopene-research/21462325.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "de4990e5a9c520e6e528e181a4e81a469a4ebac313151bfa7828ad935b04a823", "start_char": 0, "end_char": 1048, "text_sha256": "de4990e5a9c520e6e528e181a4e81a469a4ebac313151bfa7828ad935b04a823"} [lycopene-p21462325] CD36 is involved in lycopene and lutein uptake by adipocytes and adipose tissue cultures. (2011). https://pubmed.ncbi.nlm.nih.gov/21462325/ DOI: 10.1002/mnfr.201000399
Complete structured claim and evidenceDominant-negative Nrf2 abolished the carotenoid-induced rise in phase II enzymes.
Experimental context and source evidence
- availability_state
- machinery_impairment Imported condition classification; unverified.
- evidence_span
- {"source_cache": "artifacts/lycopene-research/15657364.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "a25b93d6074a1e560bf1e163aa70c511e99199b9bb62ccdffdbe70e51fcc7c32", "start_char": 0, "end_char": 1890, "text_sha256": "a25b93d6074a1e560bf1e163aa70c511e99199b9bb62ccdffdbe70e51fcc7c32"}
- experimental_model
- Reporter, expression and dominant-negative transcription-factor experiments
- exposure
- Lycopene and ethanolic derivative extract
- limitations
- Unidentified derivative extract was active; direct binding of intact lycopene to KEAP1 was not established.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human cancer cell cultures
- plain_language
- A signaling compound cannot produce this response when the experimental gene-control machinery is blocked.
- primary_references
- [lycopene-p15657364] Carotenoids activate the antioxidant response element transcription system. (2005). https://pubmed.ncbi.nlm.nih.gov/15657364/ DOI: 10.1158/1535-7163.177.4.1
- tissue_or_cell_type
- ARE transcription and phase II enzyme expression
- trigger_kind
- machinery_impairment Imported condition classification; unverified.
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 481–492
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Reporter, expression and dominant-negative transcription-factor experiments · source_derived_draft · unverified_draft
### lycopene-nrf2-required Dominant-negative Nrf2 abolished the carotenoid-induced rise in phase II enzymes. Condition category: machinery_impairment nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: A signaling compound cannot produce this response when the experimental gene-control machinery is blocked. organism: Human cancer cell cultures tissue_or_cell_type: ARE transcription and phase II enzyme expression experimental_model: Reporter, expression and dominant-negative transcription-factor experiments limitations: Unidentified derivative extract was active; direct binding of intact lycopene to KEAP1 was not established. exposure: Lycopene and ethanolic derivative extract evidence_span: {"source_cache": "artifacts/lycopene-research/15657364.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "a25b93d6074a1e560bf1e163aa70c511e99199b9bb62ccdffdbe70e51fcc7c32", "start_char": 0, "end_char": 1890, "text_sha256": "a25b93d6074a1e560bf1e163aa70c511e99199b9bb62ccdffdbe70e51fcc7c32"} [lycopene-p15657364] Carotenoids activate the antioxidant response element transcription system. (2005). https://pubmed.ncbi.nlm.nih.gov/15657364/ DOI: 10.1158/1535-7163.177.4.1
Complete structured claim and evidenceOlestra lowered serum lycopene by 12 weeks, persisting after cholesterol or BMI adjustment; the multivitamin did not prevent this.
Experimental context and source evidence
- availability_state
- biomarker_context Imported condition classification; unverified.
- evidence_span
- {"source_cache": "artifacts/lycopene-research/15930452.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "3a90148eb83ff18442e37f9fd5ed31f44acbf8d7616ef05ff1e65e6e2d64e84f", "start_char": 0, "end_char": 1595, "text_sha256": "3a90148eb83ff18442e37f9fd5ed31f44acbf8d7616ef05ff1e65e6e2d64e84f"}
- experimental_model
- Randomized 36-week controlled diet study
- exposure
- Olestra substituted for one-third of fat energy; daily multivitamin and vitamin-E-fortified olestra
- limitations
- Exposure-specific depletion, not an established lycopene deficiency syndrome; reference-range limits are not clinical deficiency thresholds.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human, 37 healthy men
- plain_language
- Replacing dietary fat with a nonabsorbed substitute changed carotenoid exposure.
- primary_references
- [lycopene-p15930452] Daily intake of multivitamins during long-term intake of olestra in men prevents declines in serum vitamins A and E but not carotenoids. (2005). https://pubmed.ncbi.nlm.nih.gov/15930452/ DOI: 10.1093/jn/135.6.1456
- tissue_or_cell_type
- Serum carotenoids and fat-soluble vitamins
- trigger_kind
- biomarker_context Imported condition classification; unverified.
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 858–869
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Randomized 36-week controlled diet study · source_derived_draft · unverified_draft
### lycopene-olestra-lycopene Olestra lowered serum lycopene by 12 weeks, persisting after cholesterol or BMI adjustment; the multivitamin did not prevent this. Condition category: biomarker_context nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: Replacing dietary fat with a nonabsorbed substitute changed carotenoid exposure. organism: Human, 37 healthy men tissue_or_cell_type: Serum carotenoids and fat-soluble vitamins experimental_model: Randomized 36-week controlled diet study limitations: Exposure-specific depletion, not an established lycopene deficiency syndrome; reference-range limits are not clinical deficiency thresholds. exposure: Olestra substituted for one-third of fat energy; daily multivitamin and vitamin-E-fortified olestra evidence_span: {"source_cache": "artifacts/lycopene-research/15930452.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "3a90148eb83ff18442e37f9fd5ed31f44acbf8d7616ef05ff1e65e6e2d64e84f", "start_char": 0, "end_char": 1595, "text_sha256": "3a90148eb83ff18442e37f9fd5ed31f44acbf8d7616ef05ff1e65e6e2d64e84f"} [lycopene-p15930452] Daily intake of multivitamins during long-term intake of olestra in men prevents declines in serum vitamins A and E but not carotenoids. (2005). https://pubmed.ncbi.nlm.nih.gov/15930452/ DOI: 10.1093/jn/135.6.1456
Complete structured claim and evidenceTomato paste produced a 3.8-fold higher chylomicron lycopene AUC than fresh tomatoes with matched lycopene and corn oil.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/9209178.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "9e44d803f52bf022b12d9bbffbe5e2832be523d37ccfbcf2187296c5fb89200f", "start_char": 0, "end_char": 985, "text_sha256": "9e44d803f52bf022b12d9bbffbe5e2832be523d37ccfbcf2187296c5fb89200f"}
- experimental_model
- Human single-meal bioavailability comparison
- exposure
- 23 mg lycopene from fresh tomato or paste with 15 g corn oil
- limitations
- Both meals contained oil; does not isolate an oil effect or establish all heating improves availability.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human
- plain_language
- Food structure matters even when the amount of lycopene is the same.
- primary_references
- [lycopene-p9209178] Lycopene is more bioavailable from tomato paste than from fresh tomatoes. (1997). https://pubmed.ncbi.nlm.nih.gov/9209178/ DOI: 10.1093/ajcn/66.1.116
- tissue_or_cell_type
- Chylomicron fraction
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 169–180
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Human single-meal bioavailability comparison · source_derived_draft · unverified_draft
### lycopene-paste-absorption Tomato paste produced a 3.8-fold higher chylomicron lycopene AUC than fresh tomatoes with matched lycopene and corn oil. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: Food structure matters even when the amount of lycopene is the same. organism: Human tissue_or_cell_type: Chylomicron fraction experimental_model: Human single-meal bioavailability comparison limitations: Both meals contained oil; does not isolate an oil effect or establish all heating improves availability. exposure: 23 mg lycopene from fresh tomato or paste with 15 g corn oil evidence_span: {"source_cache": "artifacts/lycopene-research/9209178.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "9e44d803f52bf022b12d9bbffbe5e2832be523d37ccfbcf2187296c5fb89200f", "start_char": 0, "end_char": 985, "text_sha256": "9e44d803f52bf022b12d9bbffbe5e2832be523d37ccfbcf2187296c5fb89200f"} [lycopene-p9209178] Lycopene is more bioavailable from tomato paste than from fresh tomatoes. (1997). https://pubmed.ncbi.nlm.nih.gov/9209178/ DOI: 10.1093/ajcn/66.1.116
Complete structured claim and evidenceTomato paste increased instrumental erythema D30 versus control, P=0.03.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/20854436.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "70a295ef309afb9296521357fe29b70f532c2fd215687c918b94ee027aa707ba", "start_char": 0, "end_char": 2063, "text_sha256": "70a295ef309afb9296521357fe29b70f532c2fd215687c918b94ee027aa707ba"}
- experimental_model
- Randomized tomato-paste versus olive-oil trial
- exposure
- 55 g tomato paste providing 16 mg lycopene daily in olive oil for 12 weeks
- limitations
- Whole food exposure; UV endpoints differ; not evidence that lycopene replaces sunscreen or prevents skin cancer.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human, 20 women with skin phototypes I/II
- plain_language
- A measured redness response was less sensitive after the food intervention.
- primary_references
- [lycopene-p20854436] Tomato paste rich in lycopene protects against cutaneous photodamage in humans in vivo: a randomized controlled trial. (2011). https://pubmed.ncbi.nlm.nih.gov/20854436/ DOI: 10.1111/j.1365-2133.2010.10057.x
- tissue_or_cell_type
- UV-exposed skin and biopsies
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 1183–1194
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Randomized tomato-paste versus olive-oil trial · source_derived_draft · unverified_draft
### lycopene-skin-d30 Tomato paste increased instrumental erythema D30 versus control, P=0.03. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: A measured redness response was less sensitive after the food intervention. organism: Human, 20 women with skin phototypes I/II tissue_or_cell_type: UV-exposed skin and biopsies experimental_model: Randomized tomato-paste versus olive-oil trial limitations: Whole food exposure; UV endpoints differ; not evidence that lycopene replaces sunscreen or prevents skin cancer. exposure: 55 g tomato paste providing 16 mg lycopene daily in olive oil for 12 weeks evidence_span: {"source_cache": "artifacts/lycopene-research/20854436.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "70a295ef309afb9296521357fe29b70f532c2fd215687c918b94ee027aa707ba", "start_char": 0, "end_char": 2063, "text_sha256": "70a295ef309afb9296521357fe29b70f532c2fd215687c918b94ee027aa707ba"} [lycopene-p20854436] Tomato paste rich in lycopene protects against cutaneous photodamage in humans in vivo: a randomized controlled trial. (2011). https://pubmed.ncbi.nlm.nih.gov/20854436/ DOI: 10.1111/j.1365-2133.2010.10057.x
Complete structured claim and evidenceThe visually assessed minimal erythema dose did not differ significantly between groups.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/20854436.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "70a295ef309afb9296521357fe29b70f532c2fd215687c918b94ee027aa707ba", "start_char": 0, "end_char": 2063, "text_sha256": "70a295ef309afb9296521357fe29b70f532c2fd215687c918b94ee027aa707ba"}
- experimental_model
- Randomized tomato-paste versus olive-oil trial
- exposure
- 55 g tomato paste providing 16 mg lycopene daily in olive oil for 12 weeks
- limitations
- Whole food exposure; UV endpoints differ; not evidence that lycopene replaces sunscreen or prevents skin cancer.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human, 20 women with skin phototypes I/II
- plain_language
- A different redness endpoint did not show the same statistical result.
- primary_references
- [lycopene-p20854436] Tomato paste rich in lycopene protects against cutaneous photodamage in humans in vivo: a randomized controlled trial. (2011). https://pubmed.ncbi.nlm.nih.gov/20854436/ DOI: 10.1111/j.1365-2133.2010.10057.x
- tissue_or_cell_type
- UV-exposed skin and biopsies
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 1196–1207
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Randomized tomato-paste versus olive-oil trial · source_derived_draft · unverified_draft
### lycopene-skin-med-null The visually assessed minimal erythema dose did not differ significantly between groups. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: A different redness endpoint did not show the same statistical result. organism: Human, 20 women with skin phototypes I/II tissue_or_cell_type: UV-exposed skin and biopsies experimental_model: Randomized tomato-paste versus olive-oil trial limitations: Whole food exposure; UV endpoints differ; not evidence that lycopene replaces sunscreen or prevents skin cancer. exposure: 55 g tomato paste providing 16 mg lycopene daily in olive oil for 12 weeks evidence_span: {"source_cache": "artifacts/lycopene-research/20854436.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "70a295ef309afb9296521357fe29b70f532c2fd215687c918b94ee027aa707ba", "start_char": 0, "end_char": 2063, "text_sha256": "70a295ef309afb9296521357fe29b70f532c2fd215687c918b94ee027aa707ba"} [lycopene-p20854436] Tomato paste rich in lycopene protects against cutaneous photodamage in humans in vivo: a randomized controlled trial. (2011). https://pubmed.ncbi.nlm.nih.gov/20854436/ DOI: 10.1111/j.1365-2133.2010.10057.x
Complete structured claim and evidenceTomato paste reduced UV-induced MMP-1 expression versus control, P=0.04.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/20854436.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "70a295ef309afb9296521357fe29b70f532c2fd215687c918b94ee027aa707ba", "start_char": 0, "end_char": 2063, "text_sha256": "70a295ef309afb9296521357fe29b70f532c2fd215687c918b94ee027aa707ba"}
- experimental_model
- Randomized tomato-paste versus olive-oil trial
- exposure
- 55 g tomato paste providing 16 mg lycopene daily in olive oil for 12 weeks
- limitations
- Whole food exposure; UV endpoints differ; not evidence that lycopene replaces sunscreen or prevents skin cancer.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human, 20 women with skin phototypes I/II
- plain_language
- A marker linked to matrix breakdown was lower.
- primary_references
- [lycopene-p20854436] Tomato paste rich in lycopene protects against cutaneous photodamage in humans in vivo: a randomized controlled trial. (2011). https://pubmed.ncbi.nlm.nih.gov/20854436/ DOI: 10.1111/j.1365-2133.2010.10057.x
- tissue_or_cell_type
- UV-exposed skin and biopsies
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 1209–1220
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Randomized tomato-paste versus olive-oil trial · source_derived_draft · unverified_draft
### lycopene-skin-mmp1 Tomato paste reduced UV-induced MMP-1 expression versus control, P=0.04. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: A marker linked to matrix breakdown was lower. organism: Human, 20 women with skin phototypes I/II tissue_or_cell_type: UV-exposed skin and biopsies experimental_model: Randomized tomato-paste versus olive-oil trial limitations: Whole food exposure; UV endpoints differ; not evidence that lycopene replaces sunscreen or prevents skin cancer. exposure: 55 g tomato paste providing 16 mg lycopene daily in olive oil for 12 weeks evidence_span: {"source_cache": "artifacts/lycopene-research/20854436.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "70a295ef309afb9296521357fe29b70f532c2fd215687c918b94ee027aa707ba", "start_char": 0, "end_char": 2063, "text_sha256": "70a295ef309afb9296521357fe29b70f532c2fd215687c918b94ee027aa707ba"} [lycopene-p20854436] Tomato paste rich in lycopene protects against cutaneous photodamage in humans in vivo: a randomized controlled trial. (2011). https://pubmed.ncbi.nlm.nih.gov/20854436/ DOI: 10.1111/j.1365-2133.2010.10057.x
Complete structured claim and evidenceThe UV-associated mitochondrial DNA 3895-base-pair deletion decreased after tomato-paste supplementation.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/20854436.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "70a295ef309afb9296521357fe29b70f532c2fd215687c918b94ee027aa707ba", "start_char": 0, "end_char": 2063, "text_sha256": "70a295ef309afb9296521357fe29b70f532c2fd215687c918b94ee027aa707ba"}
- experimental_model
- Randomized tomato-paste versus olive-oil trial
- exposure
- 55 g tomato paste providing 16 mg lycopene daily in olive oil for 12 weeks
- limitations
- Whole food exposure; UV endpoints differ; not evidence that lycopene replaces sunscreen or prevents skin cancer.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human, 20 women with skin phototypes I/II
- plain_language
- A measured mitochondrial DNA damage endpoint improved.
- primary_references
- [lycopene-p20854436] Tomato paste rich in lycopene protects against cutaneous photodamage in humans in vivo: a randomized controlled trial. (2011). https://pubmed.ncbi.nlm.nih.gov/20854436/ DOI: 10.1111/j.1365-2133.2010.10057.x
- tissue_or_cell_type
- UV-exposed skin and biopsies
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 1222–1233
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Randomized tomato-paste versus olive-oil trial · source_derived_draft · unverified_draft
### lycopene-skin-mtdna The UV-associated mitochondrial DNA 3895-base-pair deletion decreased after tomato-paste supplementation. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: A measured mitochondrial DNA damage endpoint improved. organism: Human, 20 women with skin phototypes I/II tissue_or_cell_type: UV-exposed skin and biopsies experimental_model: Randomized tomato-paste versus olive-oil trial limitations: Whole food exposure; UV endpoints differ; not evidence that lycopene replaces sunscreen or prevents skin cancer. exposure: 55 g tomato paste providing 16 mg lycopene daily in olive oil for 12 weeks evidence_span: {"source_cache": "artifacts/lycopene-research/20854436.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "70a295ef309afb9296521357fe29b70f532c2fd215687c918b94ee027aa707ba", "start_char": 0, "end_char": 2063, "text_sha256": "70a295ef309afb9296521357fe29b70f532c2fd215687c918b94ee027aa707ba"} [lycopene-p20854436] Tomato paste rich in lycopene protects against cutaneous photodamage in humans in vivo: a randomized controlled trial. (2011). https://pubmed.ncbi.nlm.nih.gov/20854436/ DOI: 10.1111/j.1365-2133.2010.10057.x
Complete structured claim and evidenceTangerine tomato juice produced an 8.5-fold higher lycopene bioavailability response than red juice in this crossover trial.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/25620547.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "bfcae4ee14a42c46972a911970a2cd85383c1f8ded5bf95b91dbae0e5c110d82", "start_char": 0, "end_char": 1385, "text_sha256": "bfcae4ee14a42c46972a911970a2cd85383c1f8ded5bf95b91dbae0e5c110d82"}
- experimental_model
- Randomized crossover meal trial
- exposure
- 10 mg lycopene from tangerine juice, 94% cis, versus red juice, 10% cis; 12-hour sampling
- limitations
- Isomer composition and crystalline versus globular food deposition changed together; cannot isolate isomer chemistry alone.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human, 11 adults
- plain_language
- Both the shape of the molecule and its packaging in the tomato may matter.
- primary_references
- [lycopene-p25620547] Enhanced bioavailability of lycopene when consumed as cis-isomers from tangerine compared to red tomato juice, a randomized, cross-over clinical trial. (2015). https://pubmed.ncbi.nlm.nih.gov/25620547/ DOI: 10.1002/mnfr.201400658
- tissue_or_cell_type
- Plasma triglyceride-rich lipoproteins
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 182–193
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Randomized crossover meal trial · source_derived_draft · unverified_draft
### lycopene-tangerine-absorption Tangerine tomato juice produced an 8.5-fold higher lycopene bioavailability response than red juice in this crossover trial. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: Both the shape of the molecule and its packaging in the tomato may matter. organism: Human, 11 adults tissue_or_cell_type: Plasma triglyceride-rich lipoproteins experimental_model: Randomized crossover meal trial limitations: Isomer composition and crystalline versus globular food deposition changed together; cannot isolate isomer chemistry alone. exposure: 10 mg lycopene from tangerine juice, 94% cis, versus red juice, 10% cis; 12-hour sampling evidence_span: {"source_cache": "artifacts/lycopene-research/25620547.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "bfcae4ee14a42c46972a911970a2cd85383c1f8ded5bf95b91dbae0e5c110d82", "start_char": 0, "end_char": 1385, "text_sha256": "bfcae4ee14a42c46972a911970a2cd85383c1f8ded5bf95b91dbae0e5c110d82"} [lycopene-p25620547] Enhanced bioavailability of lycopene when consumed as cis-isomers from tangerine compared to red tomato juice, a randomized, cross-over clinical trial. (2015). https://pubmed.ncbi.nlm.nih.gov/25620547/ DOI: 10.1002/mnfr.201400658
Complete structured claim and evidenceVitamin-A-deficient wild-type mice accumulated more hepatic lycopene than vitamin-A-sufficient mice.
Experimental context and source evidence
- availability_state
- nutrient_deficiency Imported condition classification; unverified.
- evidence_span
- {"source_cache": "artifacts/lycopene-research/37269907.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "36b39754d4d3b4ed8721a15f8dffe03bfd387dcbef3ff50918daabb45c48e756", "start_char": 0, "end_char": 1986, "text_sha256": "36b39754d4d3b4ed8721a15f8dffe03bfd387dcbef3ff50918daabb45c48e756"}
- experimental_model
- Carotenoid-enzyme knockout comparison and vitamin-A diet experiment
- exposure
- 1 mg lycopene in cottonseed oil daily for two weeks; separate vitamin-A-deficient versus sufficient diets
- limitations
- Mouse knockout distribution does not directly quantify human cleavage; increased ISX signaling does not prove conversion to vitamin A.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Mouse
- plain_language
- A shortage of one nutrient can change the handling of another compound.
- primary_references
- [lycopene-p37269907] Lycopene Accumulation in Transgenic Mice Lacking One or Both Carotenoid Cleaving Enzymes. (2023). https://pubmed.ncbi.nlm.nih.gov/37269907/ DOI: 10.1016/j.tjnut.2023.05.025
- tissue_or_cell_type
- Liver, other tissues and intestinal gene expression
- trigger_kind
- nutrient_deficiency Imported condition classification; unverified.
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 806–817
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Carotenoid-enzyme knockout comparison and vitamin-A diet experiment · source_derived_draft · unverified_draft
### lycopene-vitamin-a-status Vitamin-A-deficient wild-type mice accumulated more hepatic lycopene than vitamin-A-sufficient mice. Condition category: nutrient_deficiency nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: A shortage of one nutrient can change the handling of another compound. organism: Mouse tissue_or_cell_type: Liver, other tissues and intestinal gene expression experimental_model: Carotenoid-enzyme knockout comparison and vitamin-A diet experiment limitations: Mouse knockout distribution does not directly quantify human cleavage; increased ISX signaling does not prove conversion to vitamin A. exposure: 1 mg lycopene in cottonseed oil daily for two weeks; separate vitamin-A-deficient versus sufficient diets evidence_span: {"source_cache": "artifacts/lycopene-research/37269907.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "36b39754d4d3b4ed8721a15f8dffe03bfd387dcbef3ff50918daabb45c48e756", "start_char": 0, "end_char": 1986, "text_sha256": "36b39754d4d3b4ed8721a15f8dffe03bfd387dcbef3ff50918daabb45c48e756"} [lycopene-p37269907] Lycopene Accumulation in Transgenic Mice Lacking One or Both Carotenoid Cleaving Enzymes. (2023). https://pubmed.ncbi.nlm.nih.gov/37269907/ DOI: 10.1016/j.tjnut.2023.05.025
Complete structured claim and evidenceCombined lycopene and alpha-tocopherol inhibited proliferation by up to about 90%; lycopene alone was weak in these cultures.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/9784387.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "51bb94173c1f98ab622ff028dfefaa016eb3fb5021f40f79e1d7d02bceaa7c15", "start_char": 0, "end_char": 701, "text_sha256": "51bb94173c1f98ab622ff028dfefaa016eb3fb5021f40f79e1d7d02bceaa7c15"}
- experimental_model
- Combined-compound proliferation assay
- exposure
- Lycopene below 1 micromolar and alpha-tocopherol 50 micromolar
- limitations
- Reported in-vitro synergy; not proof of cancer prevention or a safe/effective supplement combination.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Human DU-145 and PC-3 prostate carcinoma cells
- plain_language
- A vitamin E interaction was observed, but only in the tested cancer-cell systems.
- primary_references
- [lycopene-p9784387] Lycopene in association with alpha-tocopherol inhibits at physiological concentrations proliferation of prostate carcinoma cells. (1998). https://pubmed.ncbi.nlm.nih.gov/9784387/ DOI: 10.1006/bbrc.1998.9351
- tissue_or_cell_type
- Cultured cell proliferation
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 871–882
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Combined-compound proliferation assay · source_derived_draft · unverified_draft
### lycopene-vitamin-e-combination Combined lycopene and alpha-tocopherol inhibited proliferation by up to about 90%; lycopene alone was weak in these cultures. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: A vitamin E interaction was observed, but only in the tested cancer-cell systems. organism: Human DU-145 and PC-3 prostate carcinoma cells tissue_or_cell_type: Cultured cell proliferation experimental_model: Combined-compound proliferation assay limitations: Reported in-vitro synergy; not proof of cancer prevention or a safe/effective supplement combination. exposure: Lycopene below 1 micromolar and alpha-tocopherol 50 micromolar evidence_span: {"source_cache": "artifacts/lycopene-research/9784387.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "51bb94173c1f98ab622ff028dfefaa016eb3fb5021f40f79e1d7d02bceaa7c15", "start_char": 0, "end_char": 701, "text_sha256": "51bb94173c1f98ab622ff028dfefaa016eb3fb5021f40f79e1d7d02bceaa7c15"} [lycopene-p9784387] Lycopene in association with alpha-tocopherol inhibits at physiological concentrations proliferation of prostate carcinoma cells. (1998). https://pubmed.ncbi.nlm.nih.gov/9784387/ DOI: 10.1006/bbrc.1998.9351
Complete structured claim and evidenceLycopene AUC was reduced with the tested fibers, including pectin; the multi-fiber effect range is not a pectin-specific number.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/pectin-research/10573545.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "f0828162b0e41d10d79784cea5cc96e55409b4ee80be3afc399132a7ad087332", "start_char": 0, "end_char": 1340, "text_sha256": "f0828162b0e41d10d79784cea5cc96e55409b4ee80be3afc399132a7ad087332"}
- experimental_model
- Crossover mixed-carotenoid meal study in six healthy women
- exposure
- Pectin or other fibers at 0.15 g/kg with a carotenoid and alpha-tocopherol mixture
- limitations
- Reported effect-size ranges cover multiple fibers, not one pectin-specific estimate. Plasma exposure does not establish long-term deficiency.
- nutrient_topic
- Pectin research collection; topical membership is not evidence of a direct dietary effect. · Pectin, structurally heterogeneous plant polysaccharides
- organism
- Homo sapiens
- plain_language
- Pectin was associated with a smaller lycopene response.
- primary_references
- [pectin-p10573545] Some dietary fibers reduce the absorption of carotenoids in women. (1999). https://pubmed.ncbi.nlm.nih.gov/10573545/ DOI: 10.1093/jn/129.12.2170
- tissue_or_cell_type
- Plasma 24-hour area under the curve
Pectin: metabolism, signaling and nutrient connections (2026-09-17) · lines 685–696
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Crossover mixed-carotenoid meal study in six healthy women · source_derived_draft · unverified_draft
### pectin-lycopene-auc Lycopene AUC was reduced with the tested fibers, including pectin; the multi-fiber effect range is not a pectin-specific number. Condition category: normal nutrient_topic: Pectin research collection; topical membership is not evidence of a direct dietary effect. plain_language: Pectin was associated with a smaller lycopene response. organism: Homo sapiens tissue_or_cell_type: Plasma 24-hour area under the curve experimental_model: Crossover mixed-carotenoid meal study in six healthy women limitations: Reported effect-size ranges cover multiple fibers, not one pectin-specific estimate. Plasma exposure does not establish long-term deficiency. exposure: Pectin or other fibers at 0.15 g/kg with a carotenoid and alpha-tocopherol mixture evidence_span: {"source_cache": "artifacts/pectin-research/10573545.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "f0828162b0e41d10d79784cea5cc96e55409b4ee80be3afc399132a7ad087332", "start_char": 0, "end_char": 1340, "text_sha256": "f0828162b0e41d10d79784cea5cc96e55409b4ee80be3afc399132a7ad087332"} [pectin-p10573545] Some dietary fibers reduce the absorption of carotenoids in women. (1999). https://pubmed.ncbi.nlm.nih.gov/10573545/ DOI: 10.1093/jn/129.12.2170
Complete structured claim and evidence
The events it takes part in
A mechanism often involves more than two components. These are the full events, with every participant and its role.
Situations it appears in
Low-supply and faulty-machinery situations recorded in the chapters where this component plays a part.
In the sources
Preserved passages that mention this component, quoted exactly. Open one to read it in context.
Open hypotheses
Proposed ideas that involve this component. They are labeled as hypotheses and do not change any recorded statement.
This is a research prototype built from draft material. It is not medical advice, and its statements still await verification against the original studies.