Liang Xin-Yi, Zhang Yue, He Ya-Nan, Liu Xue-Yi, Ding Zhi-Hao, Zhang Xiao-Dong, Dong Ming-You, Du Run-Lei
Hubei Key Laboratory of Cell Homeostasis, College of Life Sciences, Wuhan University, Wuhan, China.
The Key Laboratory of Molecular Pathology (For Hepatobiliary Diseases) of Guangxi, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.
Front Genet. 2022 Sep 12;13:888601. doi: 10.3389/fgene.2022.888601. eCollection 2022.
Hepatocellular carcinoma (HCC) is the most prevalent type of primary liver cancer characterized by high mortality and morbidity rate. The lack of effective treatments and the high frequency of recurrence lead to poor prognosis of patients with HCC. Therefore, it is important to develop robust prediction tools for predicting the prognosis of HCC. Recent studies have shown that cancer stem cells (CSC) participate in HCC progression. The aim of this study was to explore the prognostic value of CSC-related genes and establish a prediction model based on data from The Cancer Genome Atlas (TCGA) database. In this study, 475 CSC-related genes were obtained from the Molecular Signature Database and 160 differentially expressed CSC-related genes in HCC patients were identified using the limma R package in the TCGA database. A total of 79 CSC-related genes were found to be associated with overall survival (OS). Using the least absolute shrinkage and selection operator (LASSO) and multivariate Cox regressions, a 3-gene signature (, and ) was constructed. Receiver operating characteristic (ROC) curves and Kaplan-Meier survival curves were constructed to test the prediction performance of the signature. Performance of the signature was validated using the International Cancer Genome Consortium (ICGC) dataset. In addition, immune feature and functional enrichment analyses were carried out to explore the underlying mechanisms. Moreover, a co-expression network was constructed using the weighted gene correlation network analysis (WGCNA) method to select genes significantly associated with risk scores in HCC in the TCGA dataset. The gene was found to be significantly associated with risk scores of HCC. experiments revealed that it can promote HCC cell proliferation. Therefore, may be a potential therapeutic target for HCC treatment. The constructed nomogram can help clinicians make decisions about HCC treatment.
肝细胞癌(HCC)是最常见的原发性肝癌类型,其死亡率和发病率都很高。缺乏有效的治疗方法以及高复发率导致HCC患者的预后较差。因此,开发强大的预测工具来预测HCC的预后非常重要。最近的研究表明,癌症干细胞(CSC)参与了HCC的进展。本研究的目的是探讨CSC相关基因的预后价值,并基于癌症基因组图谱(TCGA)数据库的数据建立一个预测模型。在本研究中,从分子特征数据库中获得了475个CSC相关基因,并使用TCGA数据库中的limma R包鉴定了HCC患者中160个差异表达的CSC相关基因。共发现79个CSC相关基因与总生存期(OS)相关。使用最小绝对收缩和选择算子(LASSO)和多变量Cox回归,构建了一个三基因特征(、和)。构建了受试者工作特征(ROC)曲线和Kaplan-Meier生存曲线来测试该特征的预测性能。使用国际癌症基因组联盟(ICGC)数据集验证了该特征的性能。此外,还进行了免疫特征和功能富集分析以探索潜在机制。此外,使用加权基因共表达网络分析(WGCNA)方法构建了一个共表达网络,以选择与TCGA数据集中HCC风险评分显著相关的基因。发现基因与HCC风险评分显著相关。实验表明它可以促进HCC细胞增殖。因此,可能是HCC治疗的潜在治疗靶点。构建的列线图可以帮助临床医生做出关于HCC治疗的决策。