Component

PCSK9 transcription

PCSK9 transcription. 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. Berberine lowered HNF1A-dependent PCSK9 transcription; proteasome inhibition prevented this response.

    Berberine → PCSK9 transcription source_derived_draftungraded
    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/berberine-research/25540198.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "08c835c28631cd0c79be4e5a602216f8eddcd0f2d0c967074d7c9faf4aa9e446", "start_char": 0, "end_char": 1769, "text_sha256": "08c835c28631cd0c79be4e5a602216f8eddcd0f2d0c967074d7c9faf4aa9e446"}
    experimental_model
    Protein-turnover and proteasome-inhibitor experiments
    exposure
    Berberine, ubiquitin assays and proteasome inhibition
    limitations
    HNF1A protein turnover differs from HNF1A gene transcription. Proteasome inhibitors are experimental probes, not suggested combination treatment.
    nutrient_topic
    Berberine research collection; topical membership is not evidence of a direct dietary effect. · Berberine
    organism
    Human HepG2 cells; separate mouse and hamster arms
    plain_language
    This route regulates a protein that controls LDL-receptor availability.
    primary_references
    [berberine-p25540198] Inhibition of PCSK9 transcription by berberine involves down-regulation of hepatic HNF1α protein expression through the ubiquitin-proteasome degradation pathway. (2015). https://pubmed.ncbi.nlm.nih.gov/25540198/ DOI: 10.1074/jbc.m114.597229
    tissue_or_cell_type
    HNF1A and PCSK9 gene regulation

    Berberine: metabolism, nutrient connections and drug interactions (2026-09-17) · lines 480–491

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Protein-turnover and proteasome-inhibitor experiments · source_derived_draft · unverified_draft

    ### berberine-pcsk9-transcription Berberine lowered HNF1A-dependent PCSK9 transcription; proteasome inhibition prevented this response. Condition category: normal nutrient_topic: Berberine research collection; topical membership is not evidence of a direct dietary effect. plain_language: This route regulates a protein that controls LDL-receptor availability. organism: Human HepG2 cells; separate mouse and hamster arms tissue_or_cell_type: HNF1A and PCSK9 gene regulation experimental_model: Protein-turnover and proteasome-inhibitor experiments limitations: HNF1A protein turnover differs from HNF1A gene transcription. Proteasome inhibitors are experimental probes, not suggested combination treatment. exposure: Berberine, ubiquitin assays and proteasome inhibition evidence_span: {"source_cache": "artifacts/berberine-research/25540198.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "08c835c28631cd0c79be4e5a602216f8eddcd0f2d0c967074d7c9faf4aa9e446", "start_char": 0, "end_char": 1769, "text_sha256": "08c835c28631cd0c79be4e5a602216f8eddcd0f2d0c967074d7c9faf4aa9e446"} [berberine-p25540198] Inhibition of PCSK9 transcription by berberine involves down-regulation of hepatic HNF1α protein expression through the ubiquitin-proteasome degradation pathway. (2015). https://pubmed.ncbi.nlm.nih.gov/25540198/ DOI: 10.1074/jbc.m114.597229
    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