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Identification of potential hub genes associated with the pathogenesis and prognosis of hepatocellular carcinoma via integrated bioinformatics analysis

机译:通过整合生物信息分析鉴定与肝细胞癌发病机制和预后相关的潜在轮毂基因

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Objective The objective was to identify potential hub genes associated with the pathogenesis and prognosis of hepatocellular carcinoma (HCC). Methods Gene expression profile datasets were downloaded from the Gene Expression Omnibus database. Differentially expressed genes (DEGs) between HCC and normal samples were identified via an integrated analysis. A protein–protein interaction network was constructed and analyzed using the STRING database and Cytoscape software, and enrichment analyses were carried out through DAVID. Gene Expression Profiling Interactive Analysis and Kaplan–Meier plotter were used to determine expression and prognostic values of hub genes. Results We identified 11 hub genes ( CDK1 , CCNB2 , CDC20 , CCNB1 , TOP2A , CCNA2 , MELK , PBK , TPX2 , KIF20A , and AURKA ) that might be closely related to the pathogenesis and prognosis of HCC. Enrichment analyses indicated that the DEGs were significantly enriched in metabolism-associated pathways, and hub genes and module 1 were highly associated with cell cycle pathway. Conclusions In this study, we identified key genes of HCC, which indicated directions for further research into diagnostic and prognostic biomarkers that could facilitate targeted molecular therapy for HCC.
机译:目的是鉴定与肝细胞癌(HCC)发病机制和预后相关的潜在轮毂基因。方法从基因表达式omnibus数据库下载基因表达谱分类数据集。通过综合分析鉴定HCC和正常样品之间的差异表达基因(DEGS)。使用串数据库和Cytoscape软件构建和分析蛋白质 - 蛋白质相互作用网络,通过大卫进行富集分析。基因表达分析互动分析和Kaplan-Meier绘图仪用于确定轮毂基因的表达和预后值。结果我们鉴定了11个枢纽基因(CDK1,CCNB2,CDC20,CCNB1,TOP2A,CCNA2,梅克,PBK,TPX2,KIF20A和AURKA),其可能与HCC发病机制和预后密切相关。富集分析表明,在新陈代谢相关途径中显着富集,轮毂基因和模块1与细胞周期途径高。在本研究中,我们确定了HCC的关键基因,这表明进一步研究诊断和预后生物标志物的方向,这些生物标志物可以促进HCC的靶向分子治疗。

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