Prognostic model for hepatocellular carcinoma based on necroptosis-related genes and analysis of drug treatment responses
- Ronghuo Wu 1, Xiaoxia Deng 2, Xiaomin Wang 3, Shanshan Li 3, Jing Su 4,5, Xiaoyan Sun 6
- Ronghuo Wu 1, Xiaoxia Deng 2, Xiaomin Wang 3
- 1Department of Economics, Jinan University, Guangzhou, 510632, China.
- 2School of Mathematics and Statistics, Yulin Normal University, Yulin, 537000, China.
- 3Department of Biology and Pharmacy, Yulin Normal University, Yulin, 537000, China.
- 4Schoole of Information and Management, Guangxi Medical University, Nanning, 530002, China.
- 5Faculty of Data Science, City University of Macau, Macao, Macao SAR, China.
- 6Human Resources Office, Guangxi Medical University, Nanning, 530002, China.
- 0Department of Economics, Jinan University, Guangzhou, 510632, China.
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View abstract on PubMed
Summary
This summary is machine-generated.This study developed a new risk model using necroptosis-related genes to predict survival and immunotherapy response in liver cancer (HCC). The model identifies potential drug sensitivities for personalized treatment strategies.
Area Of Science
- Oncology
- Molecular Biology
- Immunology
Background
- Necroptosis plays a critical role in liver cancer development, metastasis, and immune evasion.
- Liver cancer subtypes are influenced by hepatocyte apoptosis or necroptosis.
- Analysis of necroptosis-related genes in hepatocellular carcinoma (HCC) is limited.
Purpose Of The Study
- To develop a risk scoring model for HCC based on necroptosis-related genes.
- To validate the model's predictive power for overall survival and immunotherapy efficacy in HCC.
- To analyze drug treatment responses in different HCC subtypes.
Main Methods
- Utilized TCGA data for liver cancer patients, including clinical information and RNA-seq.
- Identified differentially expressed necroptosis-related genes and performed GO/KEGG enrichment.
- Employed Cox regression and LASSO analysis to build and validate a prognostic model.
- Conducted immune cell correlation analysis and ssGSEA.
- Screened potential drugs for HCC based on subtype-specific sensitivity.
Main Results
- Identified 19 differentially expressed necroptosis-related genes.
- Constructed a 3-gene predictive model demonstrating strong performance in risk stratification and survival prediction.
- ssGSEA analysis revealed significant immune cell differences.
- Evaluated 55 immunotherapy drugs, identifying distinct sensitivities for drugs like Bleomycin and Obatoclax. Mesylate across HCC subtypes.
Conclusions
- The developed necroptosis-based risk model effectively predicts prognosis and immunotherapy response in HCC.
- Drug sensitivity analysis provides valuable insights for personalized treatment strategies in HCC.
- This research offers a foundation for targeted therapies and improved clinical management of liver cancer.
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