Component

rDNA-locus methylation in human Caco-2 cells

Experimental species, exposure and limitations are retained on 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. The 2025 Caco-2 methylome analysis associated indicaxanthin exposure with increased methylation at rDNA loci.

    Experimental context and source evidence
    dose
    Indicaxanthin 10 and 50 micromolar analysis; study also includes 100 micromolar
    duration
    48 h
    evidence_access
    Primary open full text, relevant results/methods and PubMed metadata.
    evidence_scope
    literature_reviewed; model-specific source-derived curation
    experimental_model
    Human Caco-2 colorectal cancer cells; RRBS analysis
    limitations
    Same research program and related RRBS methods as the 2023 study; independent dataset replication is not established. rDNA methylation is not direct proof of reduced ribosome production or cell transdifferentiation.
    nutrient_topic
    Dedicated indicaxanthin chapter; original betalain family identity and shared claims preserved. · Indicaxanthin
    organism
    Human Caco-2 colorectal cancer cells; RRBS analysis
    plain_language
    The 2025 Caco-2 methylome analysis associated indicaxanthin exposure with increased methylation at rDNA loci.
    primary_references
    Epigenetic Remodeling of Regulatory Regions by Indicaxanthin Suggests a Shift in Cell Identity Programs in Colorectal Cancer Cells. (2025). https://pubmed.ncbi.nlm.nih.gov/40649850/ DOI: 10.3390/ijms26136072
    route
    In vitro treatment and methylome analysis
    tissue
    rDNA loci and regulatory DNA

    Indicaxanthin: mechanisms, molecular forms and cross-actor connections (2026-09-20) · lines 459–468

    Original AI-assisted curation of thirteen additional primary studies, with twenty-six existing claims from eight studies linked unchanged. Study-specific citations and limitations retained. Not publisher full text. · supports · Human Caco-2 colorectal cancer cells; RRBS analysis · source_derived_draft · unverified_draft

    ## indicaxanthin-rdna-methylation The 2025 Caco-2 methylome analysis associated indicaxanthin exposure with increased methylation at rDNA loci. Model/species: Human Caco-2 colorectal cancer cells; RRBS analysis Tissue: rDNA loci and regulatory DNA Exposure: Indicaxanthin 10 and 50 micromolar analysis; study also includes 100 micromolar Route: In vitro treatment and methylome analysis Duration: 48 h Limits: Same research program and related RRBS methods as the 2023 study; independent dataset replication is not established. rDNA methylation is not direct proof of reduced ribosome production or cell transdifferentiation. Primary reference: Epigenetic Remodeling of Regulatory Regions by Indicaxanthin Suggests a Shift in Cell Identity Programs in Colorectal Cancer Cells. (2025). https://pubmed.ncbi.nlm.nih.gov/40649850/ DOI: 10.3390/ijms26136072 Access: Primary open full text, relevant results/methods and PubMed metadata.
    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