Component

Human GRP78 / BiP / HSPA5

Human GRP78 / BiP / HSPA5. 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. Boric-acid treatment increased GRP78/BiP expression alongside the ATF6 response in DU-145 cells.

    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/boron-research/27587023.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "421c3ea56e2b1058bb780928a63bb648246560a0ba3a070d82dc3fdd37ff0725", "start_char": 0, "end_char": 1886, "text_sha256": "421c3ea56e2b1058bb780928a63bb648246560a0ba3a070d82dc3fdd37ff0725"}
    experimental_model
    Time-course immunoblotting and ER-stress gene expression
    exposure
    10 µM boric acid; early time points from 30 minutes
    limitations
    Expression changes do not establish direct molecular targets or clinical effects. Total eIF2α abundance is distinct from Ser51 phosphorylation. The study did not activate every ER-stress branch.
    nutrient_topic
    Boron research collection; topical membership is not evidence of a direct dietary effect. · Boron
    organism
    Human DU-145 cells
    plain_language
    The cells increased an ER protein-folding helper.
    primary_references
    [boron-p27587023] Activation of the EIF2α/ATF4 and ATF6 Pathways in DU-145 Cells by Boric Acid at the Concentration Reported in Men at the US Mean Boron Intake. (2017). https://pubmed.ncbi.nlm.nih.gov/27587023/ DOI: 10.1007/s12011-016-0824-y
    tissue_or_cell_type
    Prostate cancer cell culture

    Boron: chemistry, nutrient interactions, low-intake studies and mechanistic uncertainties (2026-09-17) · lines 443–454

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Time-course immunoblotting and ER-stress gene expression · source_derived_draft · unverified_draft

    ### boron-bip-expression Boric-acid treatment increased GRP78/BiP expression alongside the ATF6 response in DU-145 cells. Condition category: normal nutrient_topic: Boron research collection; topical membership is not evidence of a direct dietary effect. plain_language: The cells increased an ER protein-folding helper. organism: Human DU-145 cells tissue_or_cell_type: Prostate cancer cell culture experimental_model: Time-course immunoblotting and ER-stress gene expression limitations: Expression changes do not establish direct molecular targets or clinical effects. Total eIF2α abundance is distinct from Ser51 phosphorylation. The study did not activate every ER-stress branch. exposure: 10 µM boric acid; early time points from 30 minutes evidence_span: {"source_cache": "artifacts/boron-research/27587023.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "421c3ea56e2b1058bb780928a63bb648246560a0ba3a070d82dc3fdd37ff0725", "start_char": 0, "end_char": 1886, "text_sha256": "421c3ea56e2b1058bb780928a63bb648246560a0ba3a070d82dc3fdd37ff0725"} [boron-p27587023] Activation of the EIF2α/ATF4 and ATF6 Pathways in DU-145 Cells by Boric Acid at the Concentration Reported in Men at the US Mean Boron Intake. (2017). https://pubmed.ncbi.nlm.nih.gov/27587023/ DOI: 10.1007/s12011-016-0824-y
    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