Component

MCF7 breast cancer cell cycle progression

MCF7 breast cancer cell cycle progression. Species, exposure and limitations are retained in each linked claim.

1 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.

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.

Recorded relationships

What acts on it

  1. Lycopene delayed cell-cycle progression without accompanying apoptotic or necrotic cell death in the tested MCF7 cultures.

    Lycopene → MCF7 breast cancer cell cycle progression source_derived_draftungraded
    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 evidence

In the sources

Preserved passages that mention this component, quoted exactly. Open one to read it in context.

    This is a research prototype built from draft material. It is not medical advice, and its statements still await verification against the original studies.

    Evidence, AI assistance and curation standards