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Background <p>The etiology of HCC is multifactorial, with pathogenesis involving immune and metabolic pathways. This study developed a prognostic model based on immune- and metabolism-related genes (IMRGs) to improve personalized HCC management.</p> Methods <p>Transcriptomic data from HCC patients were obtained from TCGA (<i>n</i> = 377) and GEO (<i>n</i> = 115). Differentially expressed IMRGs between tumor and adjacent normal tissues were identified, and patients were stratified using non-negative matrix factorization (NMF). A LASSO-Cox prognostic model was constructed and validated, with assessments of immune microenvironment, therapeutic sensitivity, and functional pathways.</p> Results <p>HCC patients were classified into two subgroups with distinct immune microenvironment features. LASSO regression identified nine key prognostic genes from 54 consensus IMRGs, forming a robust risk model. High-risk patients had significantly worse survival, and the model outperformed existing immune/metabolic signatures (5-year AUC = 0.700 vs. 0.570–0.603) and clinical parameters (AUC = 0.720 vs. 0.470–0.712). Functional analysis revealed enhanced chromosome separation and nuclear division in high-risk patients, while low-risk patients showed elevated amino acid catabolism and fatty acid metabolism. High-risk patients also exhibited reduced Natural Killer cell activity and type II interferon responses but increased oxaliplatin sensitivity and 5-Fluorouracil resistance.</p> Conclusion <p>This IMRG-based prognostic model effectively predicts HCC outcomes, enabling risk stratification and personalized therapy. It demonstrates strong clinical utility, advancing precision medicine in HCC management.</p>

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A novel immune-metabolic prognostic model stratifies survival and personalizes therapy in hepatocellular carcinoma

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年8月24日

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  • Zejin Lin,
  • Jiaheng Wang,
  • Yiping Li,
  • Taijun Yi,
  • Xiaoyue Huang,
  • Chengrui Zhong,
  • Zhiping Chen,
  • Zeyu Lin

摘要

Background

The etiology of HCC is multifactorial, with pathogenesis involving immune and metabolic pathways. This study developed a prognostic model based on immune- and metabolism-related genes (IMRGs) to improve personalized HCC management.

Methods

Transcriptomic data from HCC patients were obtained from TCGA (n = 377) and GEO (n = 115). Differentially expressed IMRGs between tumor and adjacent normal tissues were identified, and patients were stratified using non-negative matrix factorization (NMF). A LASSO-Cox prognostic model was constructed and validated, with assessments of immune microenvironment, therapeutic sensitivity, and functional pathways.

Results

HCC patients were classified into two subgroups with distinct immune microenvironment features. LASSO regression identified nine key prognostic genes from 54 consensus IMRGs, forming a robust risk model. High-risk patients had significantly worse survival, and the model outperformed existing immune/metabolic signatures (5-year AUC = 0.700 vs. 0.570–0.603) and clinical parameters (AUC = 0.720 vs. 0.470–0.712). Functional analysis revealed enhanced chromosome separation and nuclear division in high-risk patients, while low-risk patients showed elevated amino acid catabolism and fatty acid metabolism. High-risk patients also exhibited reduced Natural Killer cell activity and type II interferon responses but increased oxaliplatin sensitivity and 5-Fluorouracil resistance.

Conclusion

This IMRG-based prognostic model effectively predicts HCC outcomes, enabling risk stratification and personalized therapy. It demonstrates strong clinical utility, advancing precision medicine in HCC management.