Across TCGA pan-cancer cohorts, MIR6859-3 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated MIR6859-3 data layer compared with 10 for mass-spec protein.
The strongest signal is observed in cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC), where higher MIR6859-3 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated MIR6859-3 expression acts as an unfavorable survival marker.
CESC and UCEC are the cancer types where MIR6859-3 Mutation most reproducibly stratifies survival.