Across TCGA pan-cancer cohorts, PSG5 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated PSG5 data layer compared with 22 for mass-spec protein.
The strongest signal is observed in lung squamous cell carcinoma (LUSC), where higher PSG5 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated PSG5 expression acts as an unfavorable survival marker, although some lineages such as UCEC and SKCM show a favorable association.
LUSC, UCEC, and CHOL are the cancer types where PSG5 Mutation most reproducibly stratifies survival.