A novel hypoxia-related signature for predicting prognosis, immune characteristics, and therapeutic response in hepatocellular carcinoma
TL;DR
A four-gene hypoxia-related prognostic signature was established and successfully stratified patients into high- and low-risk groups and was associated with distinct metabolic and immune characteristics in HCC.
Abstract
This study aimed to develop and validate a hypoxia-related gene signature for prognostic assessment in hepatocellular carcinoma (HCC) and to explore its associated biological characteristics and immune features. In addition, a self-established human tissue cohort was used to verify the expression stability of the identified signature genes. The TCGA-LIHC cohort was used as the training set to identify differentially expressed hypoxia-related genes associated with overall survival. Least absolute shrinkage and selection operator (LASSO) regression and Cox regression analyses were subsequently applied to construct a prognostic model. The predictive performance of the model was externally validated using the GSE14520 and GSE116174 cohorts. Functional enrichment and immune microenvironment analyses were performed to characterize the biological differences between risk groups. Furthermore, quantitative real-time PCR (qRT-PCR) was conducted in a human tissue cohort, including normal liver tissues, adjacent non-tumorous tissues, and HCC tissues, to validate the expression patterns of the four signature genes (TMEM45A, PPARGC1A, EFNA3, and STC2). A four-gene hypoxia-related prognostic signature was established and successfully stratified patients into high- and low-risk groups. Patients in the high-risk group exhibited significantly poorer overall survival in both the training and validation cohorts. Functional enrichment analyses revealed that high-risk tumors were associated with activation of pathways related to cell-cycle progression, MYC targets, epithelial–mesenchymal transition, and metabolic reprogramming. Immune analyses demonstrated increased M0 macrophage infiltration and elevated expression of multiple immune checkpoint genes in the high-risk group. qRT-PCR validation further confirmed the differential expression patterns of the four signature genes in human HCC tissues. This four-gene hypoxia-related signature demonstrated robust prognostic performance across multiple independent cohorts and was associated with distinct metabolic and immune characteristics in HCC. qRT-PCR validation further supported the expression stability of the identified genes in human tissues. These findings provide a useful framework for prognostic stratification and future investigation of hypoxia-related biological mechanisms and therapeutic strategies in HCC.