Across TCGA pan-cancer cohorts, MIR892B Mutation is linked to patient survival in 1 of 34 cancer types, making it a survival-associated MIR892B data layer compared with 4 for mass-spec protein.
The strongest signal is observed in lung adenocarcinoma (LUAD), where higher MIR892B Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated MIR892B expression acts as an unfavorable survival marker.
LUAD are the cancer types where MIR892B Mutation most reproducibly stratifies survival.