BSPRY

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, BSPRY Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated BSPRY data layer compared with 23 for mass-spec protein and 6 for mass-spec protein.

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

THCA, SCLC, and UCEC are the cancer types where BSPRY 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
THCADFSMedianAll0.1000.841<.00118view →
SCLCDFSMedianII,III,IV0.1370.602.00818view →
UCECDFSMedianAll1.0000.629.0354view →
Pink = unfavorable, green = favorable. Showing the 3 strongest of 3 lineages.

BSPRY–THCA (DFS)

Kaplan–Meier survival curve for BSPRY mutant vs wild-type samples in THCA.

Open the THCA breakdown →

Exploration