MPO

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, MPO Mutation is linked to patient survival in 8 of 34 cancer types, making it a survival-associated MPO data layer compared with 29 for mass-spec protein and 5 for mass-spec protein.

The strongest signal is observed in kidney renal clear cell carcinoma (KIRC), where higher MPO Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated MPO expression acts as an unfavorable survival marker.

KIRC, LUAD, and SCLC are the cancer types where MPO 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
KIRCOSMedianII,III,IV0.0540.806<.00148view →
LUADOSMedianIII,IV0.0570.680<.00112view →
SCLCDFSMedianII,III,IV0.1370.562.0139view →
READDFSMedianII,III,IV0.1820.792.0166view →
PRADDFSMedianAll0.4650.888<.0016view →
LIHCDFSMedianAll0.2020.559.0066view →
UCECOSMedianIV0.2310.592.0366view →
SKCMDFSMedianIII,IV0.0920.273.0204view →
Pink = unfavorable, green = favorable. Showing the 8 strongest of 8 lineages.

MPO–KIRC (OS)

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

Open the KIRC breakdown →

Exploration