BEST3

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, BEST3 Mutation is linked to patient survival in 6 of 34 cancer types, making it a survival-associated BEST3 data layer compared with 28 for mass-spec protein.

The strongest signal is observed in pancreatic adenocarcinoma (PAAD), where higher BEST3 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated BEST3 expression acts as an unfavorable survival marker.

PAAD, UCEC, and LUSC are the cancer types where BEST3 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
PAADOSMedianAll0.1320.613.00215view →
UCECOSMedianIV0.0660.755<.00112view →
LUSCOSMedianAll0.2740.729.0119view →
LGGDFSMedianAll0.1100.833<.0016view →
SKCMDFSMedianAll0.5520.743.0114view →
COADDFSMedianAll0.2580.691.0263view →
Pink = unfavorable, green = favorable. Showing the 6 strongest of 6 lineages.

BEST3–PAAD (OS)

Kaplan–Meier survival curve for BEST3 mutant vs wild-type samples in PAAD.

Open the PAAD breakdown →

Exploration