Identification of Key Genes and Prognostic Value Analysis in Hepatocellular Carcinoma by Integrated Bioinformatics Analysis

Meng Wang; Licheng Wang; Shusheng Wu; Dongsheng Zhou; Xianming Wang

doi:10.1155/2019/3518378

Identification of Key Genes and Prognostic Value Analysis in Hepatocellular Carcinoma by Integrated Bioinformatics Analysis

Int J Genomics. 2019 Nov 22:2019:3518378. doi: 10.1155/2019/3518378. eCollection 2019.

Authors

Meng Wang¹, Licheng Wang², Shusheng Wu³, Dongsheng Zhou^{3

4}, Xianming Wang^{3

4}

Affiliations

¹ General Surgery Department, Ward 3, Central Hospital of Zi Bo, Shandong 255000, China.
² Department of Urology, Tongji Hospital, Tongji University School of Medicine, Shanghai 200065, China.
³ Department of General Surgery, Shandong Provincial Qianfoshan Hospital, Shandong University, Shandong 250014, China.
⁴ Department of General Surgery, The First Affiliated Hospital of Shandong First Medical University, Shandong 250014, China.

Abstract

Emerging evidence indicates that various functional genes with altered expression are involved in the tumor progression of human cancers. This study is aimed at identifying novel key genes that may be used for hepatocellular carcinoma (HCC) diagnosis, prognosis, and targeted therapy. This study included 3 expression profiles (GSE45267, GSE74656, and GSE84402), which were obtained from the Gene Expression Omnibus (GEO). GEO2R was used to analyze the differentially expressed genes (DEGs) between HCC and normal samples. The functional and pathway enrichment analysis was performed by the Database for Annotation, Visualization and Integrated Discovery. A protein-protein interaction (PPI) network of the identified DEGs was constructed using the Search Tool for the Retrieval of Interacting Gene, and hub genes were identified. ONCOMINE and CCLE databases were used to verify the expression of the hub genes in HCC tissues and cells. Kaplan-Meier plotter was used to assess the effects of the hub genes on the overall survival of HCC patients. A total of 99 DEGs were identified from the 3 expression profiles. These DEGs were enriched with functional processes and pathways related to HCC pathogenesis. From the PPI network, 5 hub genes were identified. The expression of the 5 hub genes was all upregulated in HCC tissues and cells compared with the control tissues and cells. Kaplan-Meier survival curves indicated that high expression of cyclin-dependent kinase (CDK1), cyclin B1 (CCNB1), cyclin B2 (CCNB2), MAD2 mitotic arrest deficient-like 1 (MAD2L1), and topoisomerase IIα (TOP2A) predicted poor overall survival in HCC patients (all log-rank P < 0.01). These results revealed that the DEGs may serve as candidate key genes during HCC pathogenesis. The 5 hub genes, including CDK1, CCNB1, CCNB2, MAD2L1, and TOP2A, may serve as promising prognostic biomarkers in HCC.