DPP3

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, DPP3 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated DPP3 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 DPP3 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated DPP3 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.

OV, BLCA, and UCEC are the cancer types where DPP3 Mutation most reproducibly stratifies survival.

Mutation survival associations by lineage

Ranked by sampling consensus. AUC1 and AUC2 indicate survival in the high- and low-expression groups, respectively; the lower AUC marks the poorer-surviving group. p-values are from the log-rank test.
LineageMeasureSplitStageAUC1
high
AUC2
low
pSampling consensus
OVDFSMedianAll0.2170.542.00648view →
BLCADFSMedianAll0.1660.522.00324view →
UCECDFSMedianII,III,IV0.9240.306.0228view →
LIHCDFSMedianAll0.1110.555.0056view →
Pink = unfavorable, green = favorable. Showing the 4 strongest of 4 lineages.

DPP3–OV (DFS)

Kaplan–Meier survival curve for DPP3 mutant vs wild-type samples in OV.

Open the OV breakdown →

Exploration