Identification of Potential Key Genes Associated With the Pathogenesis and Prognosis of Gastric Cancer Based on Integrated Bioinformatics Analysis

Despite striking advances in multimodality management, gastric cancer (GC) remains the third cause of cancer mortality globally and identifying novel diagnostic and prognostic biomarkers is urgently demanded. The study aimed to identify potential key genes associated with the pathogenesis and progno...

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Published inFrontiers in genetics Vol. 9; p. 265
Main Authors Liu, Xinkui, Wu, Jiarui, Zhang, Dan, Bing, Zhitong, Tian, Jinhui, Ni, Mengwei, Zhang, Xiaomeng, Meng, Ziqi, Liu, Shuyu
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 17.07.2018
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Summary:Despite striking advances in multimodality management, gastric cancer (GC) remains the third cause of cancer mortality globally and identifying novel diagnostic and prognostic biomarkers is urgently demanded. The study aimed to identify potential key genes associated with the pathogenesis and prognosis of GC. Differentially expressed genes between GC and normal gastric tissue samples were screened by an integrated analysis of multiple gene expression profile datasets. Key genes related to the pathogenesis and prognosis of GC were identified by employing protein-protein interaction network and Cox proportional hazards model analyses. We identified nine hub genes ( , and ) which might be tightly correlated with the pathogenesis of GC. A prognostic gene signature consisted of , and was constructed with a good performance in predicting overall survivals. The findings of this study would provide some directive significance for further investigating the diagnostic and prognostic biomarkers to facilitate the molecular targeting therapy of GC.
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This article was submitted to Bioinformatics and Computational Biology, a section of the journal Frontiers in Genetics
Edited by: Alfredo Pulvirenti, Università degli Studi di Catania, Italy
Reviewed by: Matteo Giulietti, Università Politecnica delle Marche, Italy; Jianbo Pan, Johns Hopkins Medicine, United States
ISSN:1664-8021
1664-8021
DOI:10.3389/fgene.2018.00265