Ontology highlight
ABSTRACT: Objective
As a leading cause of cancer-related mortality, liver cancer was associated with metabolic dysregulation. We aimed to identify metabolism-related prognostic biomarkers and therapeutic targets.Methods
Transcriptomic data from TCGA were analyzed using EdgeR to identify differentially expressed genes (DEGs). WGCNA was applied to unveil the metabolism-related genes in liver cancer. Machine learning algorithms (RF, SVM, LASSO) refined marker genes. GSEA and ssGSEA were conducted to identify pathway associations and immune interactions of marker genes. DGIdb database predicted candidate therapeutics targeting these biomarkers. The independent queue (GSE54236) was verified as an external dataset. RT-PCR validated gene expression in clinical samples.Results
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SUBMITTER: Wang T
PROVIDER: S-EPMC12504094 | biostudies-literature | 2025
REPOSITORIES: biostudies-literature