BRD3
Overview
BRD3 (Bromodomain-Containing Protein 3) is a member of the BET (Bromodomain and Extra-Terminal) family of epigenetic readers that recognize acetylated lysine residues on histone tails and recruit transcriptional regulatory complexes. BRD3 has been identified as a significantly mutated gene in lung adenocarcinoma, with truncating loss-of-function mutations suggesting a tumor suppressor role in this context.
Alterations observed in the corpus
- Truncating (loss-of-function) mutations identified in lung adenocarcinoma WES study (Broad, 183 tumors); BRD3 was statistically significant by InVEx analysis PMID:22980975
Cancer types (linked)
- LUAD: BRD3 truncating mutations identified as significantly mutated in the Broad lung adenocarcinoma WES cohort (183 tumors); significance established by InVEx functional enrichment analysis PMID:22980975
Co-occurrence and mutual exclusivity
- Co-listed with ARID1A, SETD2, and SMARCA4 as significantly mutated chromatin-remodeling/epigenetic regulator genes in LUAD PMID:22980975
Therapeutic relevance
- BET bromodomain inhibitors (e.g., JQ1, I-BET762) target BRD3 and related BET family members; no direct therapeutic data in LUAD reported in the corpus.
Open questions
- Whether BRD3 truncating mutations act as drivers or passengers in LUAD and whether they confer sensitivity to BET inhibitors remains to be determined.
Sources
- PMID:22980975 — Lung adenocarcinoma WES (Broad Institute, 183 tumors)
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