Component

Cell-line-dependent CTH/CBS expression response to SAC

Context-specific entity; species, compartment and exposure are stated on each 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 study reported opposite CTH and CBS expression responses between the two breast cancer cell lines.

    Experimental context and source evidence
    acting_entity
    s-allylcysteine
    dose
    2.24, 3.37 or 4.50 mM SAC
    duration
    2, 4, 6, 8 or 24 hours
    evidence_access
    Primary abstract
    experimental_comparison
    SAC versus untreated cell controls
    experimental_model
    MCF-7 and MDA-MB-231 breast adenocarcinoma cells
    interpretation_status
    Source-derived research curation; not independent primary verification
    limitations
    Abstract does not resolve every time/dose direction; these must be retrieved before assigning a universal signed enzyme edge.
    nutrient_topic
    S-allylcysteine collection; species, compartment, exposure, co-substrates and manipulation remain explicit. · S-allyl-L-cysteine / SAC
    organism
    Homo sapiens
    plain_language
    The cellular background changed the direction of the response.
    primary_references
    [38397425] S-Allyl-L-Cysteine Affects Cell Proliferation and Expression of H2S-Synthetizing Enzymes in MCF-7 and MDA-MB-231 Adenocarcinoma Cell Lines. · 2024 · https://pubmed.ncbi.nlm.nih.gov/38397425/ · DOI 10.3390/biom14020188
    route
    Cell culture
    tissue_or_cell_type
    MCF-7 and MDA-MB-231 breast adenocarcinoma cells

    S-allylcysteine: sulfur signaling, redox responses and cross-nutrient mechanisms (2026-09-20) · lines 302–309

    AI-assisted research curation; primary references, access levels and experimental limitations individually identified. Not publisher full text. · supports · MCF-7 and MDA-MB-231 breast adenocarcinoma cells · source_derived_draft · unverified_draft

    ## s-allylcysteine-breast-cth-cbs-context The cellular background changed the direction of the response. The study reported opposite CTH and CBS expression responses between the two breast cancer cell lines. Model: MCF-7 and MDA-MB-231 breast adenocarcinoma cells Limitations: Abstract does not resolve every time/dose direction; these must be retrieved before assigning a universal signed enzyme edge. Evidence access: Primary abstract [38397425] S-Allyl-L-Cysteine Affects Cell Proliferation and Expression of H2S-Synthetizing Enzymes in MCF-7 and MDA-MB-231 Adenocarcinoma Cell Lines. · 2024 · https://pubmed.ncbi.nlm.nih.gov/38397425/ · DOI 10.3390/biom14020188 Structured context: {"organism": "Homo sapiens", "tissue_or_cell_type": "MCF-7 and MDA-MB-231 breast adenocarcinoma cells", "dose": "2.24, 3.37 or 4.50 mM SAC", "duration": "2, 4, 6, 8 or 24 hours", "route": "Cell culture", "experimental_comparison": "SAC versus untreated cell controls", "acting_entity": "s-allylcysteine", "interpretation_status": "Source-derived research curation; not independent primary verification"}
    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