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ABSTRACT: Background
Abnormal accumulation of copper could induce cell death and tumor growth, and affect tumor immune escape by regulating programmed cell death ligand 1 (PD-L1) expression. This study aims to establish and verify a risk signature based on cuproptosis- and immune-related genes (CIRGs) for hepatocellular carcinoma (HCC) management.Methods
HCC RNA-seq and clinical data were obtained from open databases. Least absolute shrinkage and selection operator (LASSO) and Cox regression analyses were utilized to screen CIRGs and develop a risk signature. The signature's value for clinical applications, functional enrichment, tumor mutation burden (TMB), and immune profile analyses were investigated systematically.Results
A risk signature was developed utilizing seven CIR
SUBMITTER: Cheng Q
PROVIDER: S-EPMC11231767 | biostudies-literature | 2024 Jun
REPOSITORIES: biostudies-literature