ACE

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, ACE Mutation is linked to patient survival in 7 of 34 cancer types, making it a survival-associated ACE data layer compared with 24 for mass-spec protein and 6 for mass-spec protein.

The strongest signal is observed in kidney renal clear cell carcinoma (KIRC), where higher ACE Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated ACE expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.

KIRC, PAAD, and BLCA are the cancer types where ACE 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
KIRCDFSMedianAll0.1230.796<.00136view →
PAADOSMedianAll0.1100.640<.00124view →
BLCAOSMedianAll0.0690.688<.00118view →
UCECDFSMedianAll0.9320.607.00812view →
TGCTDFSMedianII,III,IV0.0880.917.0106view →
LUSCDFSMedianII,III,IV0.1990.748.0063view →
SKCMOSMedianIV0.4150.861.0143view →
Pink = unfavorable, green = favorable. Showing the 7 strongest of 7 lineages.

ACE–KIRC (DFS)

Kaplan–Meier survival curve for ACE mutant vs wild-type samples in KIRC.

Open the KIRC breakdown →

Exploration