Yi Yao, KaiQing Yang, Qiang Wang, Zeming Zhu, Sheng Li, Bin Li, Bin Feng, Caixi Tang
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引用次数: 0
Abstract
This study aims to identify the cancer-associated fibroblasts (CAF)-related genes that can affect immunotherapy and drug sensitivity in hepatocellular carcinoma (HCC). Expression data and survival data associated with HCC were obtained in The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) databases. Weighted correlation network analysis (WGCNA) analysis was performed to obtain CAF-related genes. Least Absolute Shrinkage and Selection Operator (LASSO) regression was used for regression analysis and risk models. Subsequently, Gene Set Enrichment Analysis (GSEA) analysis, Gene Set Enrichment Analysis (ssGSEA) analysis, Tumor Immune Dysfunction and Exclusion (TIDE) analysis and drug sensitivity analysis were performed on the risk models. Survival analysis of CAF scores showed that the survival rate was lower in samples with high CAF scores than those with low scores. However, this difference was not significant, suggesting CAF may not directly influence the prognosis of HCC patients. Further screening of CAF-related genes yielded 33 CAF-related genes. Seven risk models constructed based on CDR2L, SPRED1, PFKP, ENG, KLF2, FSCN1 and VCAN, showed significant differences in immunotherapy and partial drug sensitivity in HCC. Seven CAF-related genes may have important roles in immunotherapy, drug sensitivity and prognostic survival in HCC patients.
本研究旨在确定可影响肝细胞癌(HCC)免疫疗法和药物敏感性的癌症相关成纤维细胞(CAF)相关基因。研究人员从癌症基因组图谱(TCGA)和基因表达总库(GEO)数据库中获得了与肝癌相关的表达数据和生存数据。通过加权相关网络分析(WGCNA)获得与CAF相关的基因。采用最小绝对收缩和选择操作器(LASSO)回归法进行回归分析和建立风险模型。随后,对风险模型进行了基因组富集分析(Gene Set Enrichment Analysis,GSEA)分析、基因组富集分析(Gene Set Enrichment Analysis,ssGSEA)分析、肿瘤免疫功能障碍和排斥(Tumor Immune Dysfunction and Exclusion,TIDE)分析以及药物敏感性分析。CAF 评分的生存率分析表明,CAF 评分高的样本生存率低于评分低的样本。然而,这一差异并不显著,表明CAF可能不会直接影响HCC患者的预后。对CAF相关基因的进一步筛选发现了33个CAF相关基因。根据CDR2L、SPRED1、PFKP、ENG、KLF2、FSCN1和VCAN构建的七个风险模型显示,这七个基因对HCC的免疫治疗和部分药物敏感性存在显著差异。七个CAF相关基因可能在HCC患者的免疫治疗、药物敏感性和预后生存中发挥重要作用。
期刊介绍:
Genes & Immunity emphasizes studies investigating how genetic, genomic and functional variations affect immune cells and the immune system, and associated processes in the regulation of health and disease. It further highlights articles on the transcriptional and posttranslational control of gene products involved in signaling pathways regulating immune cells, and protective and destructive immune responses.