Component
Human DELE1 cleavage readout
Study-specific role and exposure are specified 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.
Other things that act on it
Enzymes, hormones, genes, and other components with a recorded effect. These are not nutrients, so they do not count toward the arrows above. Each finding names the chapter that recorded it.
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.
What acts on it
SLC25A39 knockout attenuated hypoxia-associated DELE1 cleavage in HEK293T cells.
Experimental context and source evidence
- access_level
- selected_indexed_full_text_passages
- evidence_cache
- artifacts/discovery-research/round2-sources/primary-mechanism-passages.json; SHA256 81c0207494f0b2a22fd0af0d70528a5114dfd74367dd99f967f4ada68c53e8c3
- experimental_model
- Endogenous DELE1-HA HEK293T
- exposure
- 1% oxygen; exact panel times unresolved
- limitations
- Selected indexed primary full-text passages reviewed; supplements not independently inspected in this round. These records do not demonstrate iron-chelation rescue of SLC25A39 loss, clinical benefit, or transfer to pulmonary endothelium.
- organism
- Human cultured cells; mouse xenograft host only for colonization endpoint
- plain_language
- SLC25A39 knockout attenuated hypoxia-associated DELE1 cleavage in HEK293T cells.
- primary_locator
- https://pmc.ncbi.nlm.nih.gov/articles/PMC12396134/ Figure 4F
- primary_references
- https://doi.org/10.1158/2159-8290.CD-24-1556
DELE1 bridge: iron sensing and mitochondrial-glutathione-dependent stress signaling · lines 43–52
Targeted primary-literature curation; selected indexed full-text passages, 2026-09-20. · supports · Endogenous DELE1-HA HEK293T · source_derived_draft · unverified_draft
SLC25A39 knockout attenuated hypoxia-associated DELE1 cleavage in HEK293T cells. primary_references: https://doi.org/10.1158/2159-8290.CD-24-1556 primary_locator: https://pmc.ncbi.nlm.nih.gov/articles/PMC12396134/ Figure 4F evidence_cache: artifacts/discovery-research/round2-sources/primary-mechanism-passages.json; SHA256 81c0207494f0b2a22fd0af0d70528a5114dfd74367dd99f967f4ada68c53e8c3 access_level: selected_indexed_full_text_passages experimental_model: Endogenous DELE1-HA HEK293T organism: Human cultured cells; mouse xenograft host only for colonization endpoint exposure: 1% oxygen; exact panel times unresolved limitations: Selected indexed primary full-text passages reviewed; supplements not independently inspected in this round. These records do not demonstrate iron-chelation rescue of SLC25A39 loss, clinical benefit, or transfer to pulmonary endothelium. plain_language: SLC25A39 knockout attenuated hypoxia-associated DELE1 cleavage in HEK293T cells.
Complete structured claim and evidence
The events it takes part in
A mechanism often involves more than two components. These are the full events, with every participant and its role.
Situations it appears in
Low-supply and faulty-machinery situations recorded in the chapters where this component plays a part.
In the sources
Preserved passages that mention this component, quoted exactly. Open one to read it in context.
Open hypotheses
Proposed ideas that involve this component. They are labeled as hypotheses and do not change any recorded statement.
This is a research prototype built from draft material. It is not medical advice, and its statements still await verification against the original studies.