ITGB4

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, ITGB4 Mutation is linked to patient survival in 10 of 34 cancer types, making it a survival-associated ITGB4 data layer compared with 20 for mass-spec protein and 5 for mass-spec protein.

The strongest signal is observed in adrenocortical carcinoma (ACC), where higher ITGB4 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated ITGB4 expression acts as an unfavorable survival marker, although some lineages such as UCEC and STAD show a favorable association.

ACC, DLBC, and UCEC are the cancer types where ITGB4 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
ACCDFSMedianAll0.0460.753<.00136view →
DLBCDFSMedianII,III,IV0.0650.829<.00124view →
UCECDFSMedianAll0.9630.826.01216view →
LUSCDFSMedianIII,IV0.0790.751.02412view →
PRADDFSMedianAll0.0850.774<.0016view →
STADOSMedianIV0.8050.283.0316view →
LIHCOSMedianIII,IV0.0510.616<.0016view →
LUADOSMedianII,III,IV0.0900.677<.0016view →
CHOLOSMedianAll0.1550.725.0293view →
SKCMDFSMedianAll0.4910.650.0401view →
Pink = unfavorable, green = favorable. Showing the 10 strongest of 10 lineages.

ITGB4–ACC (DFS)

Kaplan–Meier survival curve for ITGB4 mutant vs wild-type samples in ACC.

Open the ACC breakdown →

Exploration