Component

Geranylgeraniol / GGOH

Isoprenoid alcohol used to restore geranylgeranylation downstream of a blocked mevalonate pathway.

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 it acts on

  1. Geranylgeraniol fully reverted statin-mediated loss of myoblast viability, while water-soluble cholesterol did not, and statins caused loss of prenylated RAP1.

    Geranylgeraniol / GGOH → C2C12 myoblast viability source_derived_draftungraded
    Experimental context and source evidence
    duration
    Not stated here
    evidence_access
    Primary PubMed abstract and indexed metadata reviewed. Full-text method details not stated here remain unresolved.
    experimental_model
    Murine C2C12 myoblasts
    exposure
    Geranylgeraniol, farnesol, mevalonate or water-soluble cholesterol co-treatment with statin
    limitations
    Cholesterol rescued only methyl-beta-cyclodextrin toxicity, and geranylgeranyltransferase inhibition with GGTI-286 could not be reversed by geranylgeraniol, so the rescue requires the transferase to be intact.
    organism
    Murine C2C12 myoblasts
    plain_language
    Geranylgeraniol fully reverted statin-mediated loss of myoblast viability, while water-soluble cholesterol did not, and statins caused loss of prenylated RAP1.
    primary_references
    Geranylgeraniol Prevents Statin-Dependent Myotoxicity in C2C12 Muscle Cells through RAP1 GTPase Prenylation and Cytoskeletal Stabilization. (2018). https://pubmed.ncbi.nlm.nih.gov/29951166/ DOI: 10.1155/2018/6463807
    route
    In vitro
    tissue
    Prenylation of RAP1 and muscle cell viability

    Atorvastatin: mechanism of action from target occupancy to isoprenoids, transport, muscle and metabolism (2026-09-22) · lines 122–131

    Original AI-assisted curation of twelve primary studies resolved by PubMed title search and cross-checked against live PubMed metadata. Findings obtained with mevastatin, simvastatin or the statin class are recorded against those subjects. Study-specific citations, doses, negative findings and limitations retained. Not publisher full text. · supports · · source_derived_draft · unverified_draft

    ## geranylgeraniol-rescues-statin-myotoxicity Geranylgeraniol fully reverted statin-mediated loss of myoblast viability, while water-soluble cholesterol did not, and statins caused loss of prenylated RAP1. Model/species: Murine C2C12 myoblasts Tissue/system: Prenylation of RAP1 and muscle cell viability Exposure: Geranylgeraniol, farnesol, mevalonate or water-soluble cholesterol co-treatment with statin Route: In vitro Duration: Not stated here Limits: Cholesterol rescued only methyl-beta-cyclodextrin toxicity, and geranylgeranyltransferase inhibition with GGTI-286 could not be reversed by geranylgeraniol, so the rescue requires the transferase to be intact. Primary reference: Geranylgeraniol Prevents Statin-Dependent Myotoxicity in C2C12 Muscle Cells through RAP1 GTPase Prenylation and Cytoskeletal Stabilization. (2018). https://pubmed.ncbi.nlm.nih.gov/29951166/ DOI: 10.1155/2018/6463807 Access: Primary PubMed abstract and indexed metadata reviewed. Full-text method details not stated here remain unresolved.
    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