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Weighted correlation gene network analysis reveals a new stemness index-related survival model for prognostic prediction in hepatocellular carcinoma

机译:加权相关基因网络分析揭示了肝细胞癌预后预测的新茎秆指数相关的存活模型

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摘要

In this study, we constructed a new survival model using mRNA expression-based stemness index (mRNAsi) for prognostic prediction in hepatocellular carcinoma (HCC). Weighted correlation network analysis (WGCNA) of HCC transcriptome data (374 HCC and 50 normal liver tissue samples) from the TCGA database revealed 7498 differentially expressed genes (DEGs) that clustered into seven gene modules. LASSO regression analysis of the top two gene modules identified , , , and as the top five mRNAsi-related genes. We constructed our survival model with these five genes and tested its performance using 243 HCC and 202 normal liver samples from the ICGC database. Kaplan-Meier survival curve and receive operating characteristic curve analyses showed that the survival model accurately predicted the prognosis and survival of high- and low-risk HCC patients with high sensitivity and specificity. The expression of these five genes was significantly higher in the HCC tissues from the TCGA, ICGC, and GEO datasets ( and ) than in normal liver tissues. These findings demonstrate that a new survival model derived from five strongly correlating mRNAsi-related genes provides highly accurate prognoses for HCC patients.
机译:在该研究中,我们使用基于mRNA表达的茎秆指数(MRNASI)构建了一种新的存活模型,用于肝细胞癌(HCC)的预后预测。来自TCGA数据库的HCC转录组数据(374HCC和50正常肝组织样本)的加权相关网络分析(374HCC和50正常肝组织样本)揭示了聚集成七种基因模块的7498个差异表达基因(DEGS)。左旋两种基因模块的套索回归分析,以及前五个MRNASI相关基因。我们用这五个基因构建了我们的生存模型,并使用243 HCC和202个正常肝脏样本从ICGC数据库进行测试。 Kaplan-Meier生存曲线和接受操作特征曲线分析表明,存活模型准确地预测了高敏感性和特异性高风险HCC患者的预后和存活。来自TCGA,ICGC和Geo Datasets(AND)的HCC组织中,这五种基因的表达显着高于正常肝组织。这些发现表明,来自五种强烈相关的MRNASI相关基因的新存活模型为HCC患者提供了高精度的预测。

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