LDLR

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, LDLR Mutation is linked to patient survival in 11 of 34 cancer types, making it a survival-associated LDLR data layer compared with 24 for mass-spec protein and 5 for mass-spec protein.

The strongest signal is observed in ovarian serous cystadenocarcinoma (OV), where higher LDLR Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated LDLR expression acts as an unfavorable survival marker, although some lineages such as UCEC and SKCM show a favorable association.

OV, HNSC, and SCLC are the cancer types where LDLR 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
OVOSMedianIV0.0070.760<.00130view →
HNSCDFSMedianAll0.1470.697<.00127view →
SCLCOSMedianII,III,IV0.0550.702<.00124view →
LUSCOSMedianIV0.0010.673.01418view →
LUADOSMedianII,III,IV0.1580.750<.00118view →
LIHCOSMedianAll0.1440.688.0139view →
UCECOSMedianII,III,IV0.9280.461.0368view →
PRADDFSMedianAll0.6170.886.0456view →
STADOSMedianIII,IV0.0030.630<.0016view →
ACCDFSMedianAll0.1400.666.0493view →
SKCMDFSMedianIII,IV0.7640.245.0401view →
Pink = unfavorable, green = favorable. Showing the 11 strongest of 11 lineages.

LDLR–OV (OS)

Kaplan–Meier survival curve for LDLR mutant vs wild-type samples in OV.

Open the OV breakdown →

Exploration