T. T. Nguyen, Nga Vu, T. Tran, Hieu T. Hoang, H. Bui
{"title":"Screening and Identification of Key Genes in Hepatitis B Virus-Related Hepatocellular Carcinoma Through an Integrated Bioinformatics Approach","authors":"T. T. Nguyen, Nga Vu, T. Tran, Hieu T. Hoang, H. Bui","doi":"10.31557/apjcb.2022.7.2.143-149","DOIUrl":null,"url":null,"abstract":"Objective: Primary liver cancer is one of the main causes of cancer mortality globally, with hepatocellular carcinoma (HCC) being the most frequent type. Chronic hepatitis B virus (HBV) infection is leading cause of HCC. This study aimed to identify significant genes for predicting prognosis in HBV-associated HCC. Methods: The GSE121248 gene expression profile was obtained from the Gene Expression Omnibus (GEO) database. Differentially expressed genes (DEGs) for HBV-associated HCC were identified by analyzing this expression profile. Enrichment analyses were performed to discover the role of DEGs in biological processes, cell components, molecular functions, and pathways. Then, protein-protein interaction (PPI) was constructed and 5 hub genes were identified. Finally, survival analysis was conducted to validate the prognostic value of these genes. Results: A total of 20188 official gene symbols were found, and 119 DEGs were identified between HBV-associated HCC and normal liver tissues. The PPI network identified CCNB1, CDK1, TOP2A, RACGAP1, and ASPM as hub genes. Kaplan-Meier curves showed that the high expression of the hub genes had significantly lower survival. Conclusion: CCNB1, CDK1, TOP2A, RACGAP1, and ASPM could be potential prognostic biomarkers and therapeutic targets for HBV-associated HCC.","PeriodicalId":8848,"journal":{"name":"Asian Pacific Journal of Cancer Biology","volume":"15 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-06-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Asian Pacific Journal of Cancer Biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.31557/apjcb.2022.7.2.143-149","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2
Abstract
Objective: Primary liver cancer is one of the main causes of cancer mortality globally, with hepatocellular carcinoma (HCC) being the most frequent type. Chronic hepatitis B virus (HBV) infection is leading cause of HCC. This study aimed to identify significant genes for predicting prognosis in HBV-associated HCC. Methods: The GSE121248 gene expression profile was obtained from the Gene Expression Omnibus (GEO) database. Differentially expressed genes (DEGs) for HBV-associated HCC were identified by analyzing this expression profile. Enrichment analyses were performed to discover the role of DEGs in biological processes, cell components, molecular functions, and pathways. Then, protein-protein interaction (PPI) was constructed and 5 hub genes were identified. Finally, survival analysis was conducted to validate the prognostic value of these genes. Results: A total of 20188 official gene symbols were found, and 119 DEGs were identified between HBV-associated HCC and normal liver tissues. The PPI network identified CCNB1, CDK1, TOP2A, RACGAP1, and ASPM as hub genes. Kaplan-Meier curves showed that the high expression of the hub genes had significantly lower survival. Conclusion: CCNB1, CDK1, TOP2A, RACGAP1, and ASPM could be potential prognostic biomarkers and therapeutic targets for HBV-associated HCC.
目的:原发性肝癌是全球癌症死亡的主要原因之一,其中肝细胞癌(HCC)是最常见的类型。慢性乙型肝炎病毒(HBV)感染是HCC的主要原因。本研究旨在确定预测hbv相关HCC预后的重要基因。方法:从gene expression Omnibus (GEO)数据库中获取GSE121248基因表达谱。通过分析这种表达谱,确定了hbv相关HCC的差异表达基因(DEGs)。进行富集分析以发现deg在生物过程,细胞成分,分子功能和途径中的作用。然后构建蛋白-蛋白相互作用(PPI),鉴定出5个枢纽基因。最后,进行生存分析以验证这些基因的预后价值。结果:共发现20188个官方基因符号,在hbv相关HCC与正常肝组织之间鉴定出119个基因符号。PPI网络鉴定出CCNB1、CDK1、TOP2A、RACGAP1和ASPM为枢纽基因。Kaplan-Meier曲线显示,hub基因的高表达显著降低了存活率。结论:CCNB1、CDK1、TOP2A、RACGAP1和ASPM可能是hbv相关性HCC的潜在预后生物标志物和治疗靶点。