Across TCGA pan-cancer cohorts, RUNX3 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated RUNX3 data layer compared with 20 for mass-spec protein and 6 for mass-spec protein.
The strongest signal is observed in uterine corpus endometrial carcinoma (UCEC), where higher RUNX3 Mutation is associated with better disease-free survival. In most high-consensus cancer types, elevated RUNX3 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
UCEC, LIHC, and LUSC are the cancer types where RUNX3 Mutation most reproducibly stratifies survival.