IPO8

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, IPO8 Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated IPO8 data layer compared with 24 for mass-spec protein and 6 for mass-spec protein.

The strongest signal is observed in liver hepatocellular carcinoma (LIHC), where higher IPO8 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated IPO8 expression acts as an unfavorable survival marker, although some lineages such as UCEC and STAD show a favorable association.

LIHC, UCEC, and LUSC are the cancer types where IPO8 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
LIHCOSMedianAll0.1040.779<.00142view →
UCECDFSMedianII,III,IV0.9360.431.01024view →
LUSCOSMedianIII,IV0.1470.664.02812view →
STADDFSMedianIV1.0000.284.0382view →
COADDFSMedianAll1.0000.776.0411view →
Pink = unfavorable, green = favorable. Showing the 5 strongest of 5 lineages.

IPO8–LIHC (OS)

Kaplan–Meier survival curve for IPO8 mutant vs wild-type samples in LIHC.

Open the LIHC breakdown →

Exploration