Thioredoxin reductase 1
Thioredoxin reductase keeps cells' antioxidant defences charged; arsenic trioxide, the drug that cures most acute promyelocytic leukaemia with ATRA, inhibits it as one of its several actions. This dossier gathers the 0 products (0 approved), 0 trials, 0 pathways and 0 resistance routes in the corpus that involve it, with external identifiers so it can be joined to UniProt, ChEMBL, Open Targets and the rest of biology.
Biology
A cytosolic flavoenzyme that uses NADPH to reduce thioredoxin; it supports DNA synthesis through ribonucleotide reductase and buffers reactive oxygen species.
- All cells, highest in tumours with high oxidative metabolism
- Acute promyelocytic leukaemia treated with arsenic trioxide
External identifiers
Built from HGNC, Ensembl, UniProt and ChEMBL idsProducts by modality and phase
Browse products →No product in the corpus is aimed at this target yet.
Trials
Evidence ranking →No trial in the corpus names this target or one of its products.
Resistance routes
Unaddressed routes →The resistance atlas has no route that names this target.
Pathways
Pathway-to-drug matrix →No pathway diagram carries this target as a node.
Companion diagnostics
Assay registry →No companion diagnostic in the registry measures this target.
Preclinical models
All models →No model entry for this target yet; check the cancer entries on the models page.
Open questions
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Literature
Preprints →Query for this target: (TITLE:"Thioredoxin reductase 1" OR ABSTRACT:"Thioredoxin reductase 1" OR TITLE:"TXNRD1" OR ABSTRACT:"TXNRD1") AND (cancer OR tumor OR tumour OR oncology OR carcinoma OR lymphoma OR leukemia OR leukaemia OR myeloma OR sarcoma OR melanoma OR glioma). Results are unfiltered search hits about Thioredoxin reductase 1, not a curated reading list.
Export
The dossier as machine-readable JSON: identifiers from HGNC, Ensembl, UniProt and ChEMBL, products with status, trials, pathways, hotspots, open questions and assays. The full entity record is in the open API at /api/v1/entities/txnrd1.json. Licence CC BY-NC 4.0.