Across TCGA pan-cancer cohorts, SAMM50 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated SAMM50 data layer compared with 25 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in ovarian serous cystadenocarcinoma (OV), where higher SAMM50 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated SAMM50 expression acts as an unfavorable survival marker.
OV, PAAD, and PRAD are the cancer types where SAMM50 Mutation most reproducibly stratifies survival.