Li Jiaming, Tan Rongzhi, Wu Jie, Guo Wenjie, Wang Yupeng, You Guoxing, Zhang Yuting, Yu Zhiyong, Geng Yan, Zan Jie, Su Jianfen
School of Biomedical and Pharmaceutical Sciences, Guangdong University of Technology, Guangzhou, China.
Department of Pharmacy, Guangzhou Panyu Central Hospital, Guangzhou, China.
Front Genet. 2023 Jan 12;13:1099148. doi: 10.3389/fgene.2022.1099148. eCollection 2022.
Hepatocellular carcinoma (HCC) is the most common type of primary liver cancer with low 5-year survival rate. Cellular senescence, characterized by permanent and irreversible cell proliferation arrest, plays an important role in tumorigenesis and development. This study aims to develop a cellular senescence-based stratified model, and a multivariable-based nomogram for guiding clinical therapy for HCC. The mRNAs expression data of HCC patients and cellular senescence-related genes were obtained from TCGA and CellAge database, respectively. Through multiple analysis, a four cellular senescence-related genes-based prognostic stratified model was constructed and its predictive performance was validated through various methods. Then, a nomogram based on the model was constructed and HCC patients stratified by the model were analyzed for tumor mutation burden, tumor microenvironment, immune infiltration, drug sensitivity and immune checkpoint. Functional enrichment analysis was performed to explore potential biological pathways. Finally, we verified this model by siRNA transfection, scratch assay and Transwell Assay. We established an cellular senescence-related genes-based stratified model, and a multivariable-based nomogram, which could accurately predict the prognosis of HCC patients in the ICGC database. The low and high risk score HCC patients stratified by the model showed different tumor mutation burden, tumor microenvironment, immune infiltration, drug sensitivity and immune checkpoint expressions. Functional enrichment analysis suggested several biological pathways related to the process and prognosis of HCC. Scratch assay and transwell assay indicated the promotion effects of the four cellular senescence-related genes (EZH2, G6PD, CBX8, and NDRG1) on the migraiton and invasion of HCC. We established a cellular senescence-based stratified model, and a multivariable-based nomogram, which could predict the survival of HCC patients and guide clinical treatment.
肝细胞癌(HCC)是最常见的原发性肝癌类型,5年生存率较低。细胞衰老以永久性和不可逆的细胞增殖停滞为特征,在肿瘤发生和发展中起重要作用。本研究旨在建立一种基于细胞衰老的分层模型和一种基于多变量的列线图,以指导HCC的临床治疗。分别从TCGA和CellAge数据库获取HCC患者的mRNA表达数据和细胞衰老相关基因。通过多重分析,构建了一个基于四个细胞衰老相关基因的预后分层模型,并通过多种方法验证了其预测性能。然后,基于该模型构建列线图,并对按该模型分层的HCC患者进行肿瘤突变负担、肿瘤微环境、免疫浸润、药物敏感性和免疫检查点分析。进行功能富集分析以探索潜在的生物学途径。最后,我们通过siRNA转染、划痕试验和Transwell试验验证了该模型。我们建立了一个基于细胞衰老相关基因的分层模型和一个基于多变量的列线图,该模型能够准确预测ICGC数据库中HCC患者的预后。按该模型分层的低风险和高风险评分HCC患者表现出不同的肿瘤突变负担、肿瘤微环境、免疫浸润、药物敏感性和免疫检查点表达。功能富集分析提示了几条与HCC发生过程和预后相关的生物学途径。划痕试验和Transwell试验表明四个细胞衰老相关基因(EZH2、G6PD、CBX8和NDRG1)对HCC迁移和侵袭的促进作用。我们建立了一个基于细胞衰老的分层模型和一个基于多变量的列线图,该模型可以预测HCC患者的生存并指导临床治疗。