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Identification of UBE2C as hub gene in driving prostate cancer by integrated bioinformatics analysis

BACKGROUND: The aim of this study was to identify novel genes in promoting primary prostate cancer (PCa) progression and to explore its role in the prognosis of prostate cancer. METHODS: Four microarray datasets containing primary prostate cancer samples and benign prostate samples were downloaded f...

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Autores principales: Wang, Yan, Wang, Jili, Tang, Qiusu, Ren, Guoping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7906463/
https://www.ncbi.nlm.nih.gov/pubmed/33630978
http://dx.doi.org/10.1371/journal.pone.0247827
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author Wang, Yan
Wang, Jili
Tang, Qiusu
Ren, Guoping
author_facet Wang, Yan
Wang, Jili
Tang, Qiusu
Ren, Guoping
author_sort Wang, Yan
collection PubMed
description BACKGROUND: The aim of this study was to identify novel genes in promoting primary prostate cancer (PCa) progression and to explore its role in the prognosis of prostate cancer. METHODS: Four microarray datasets containing primary prostate cancer samples and benign prostate samples were downloaded from Gene Expression Omnibus (GEO), then differentially expressed genes (DEGs) were identified by R software (version 3.6.2). Gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) were performed to identify the function of DEGs. Using STRING and Cytoscape (version 3.7.1), we constructed a protein-protein interaction (PPI) network and identified the hub gene of prostate cancer. Clinical data on GSE70770 and TCGA was collected to show the role of hub gene in prostate cancer progression. The correlations between hub gene and clinical parameters were also indicated by cox regression analysis. Gene Set Enrichment Analysis (GSEA) was performed to highlight the function of Ubiquitin-conjugating enzyme complex (UBE2C) in prostate cancer. RESULTS: 243 upregulated genes and 298 downregulated genes that changed in at least two microarrays have been identified. GO and KEGG analysis indicated significant changes in the oxidation-reduction process, angiogenesis, TGF-beta signaling pathway. UBE2C, PDZ-binding kinase (PBK), cyclin B1 (CCNB1), Cyclin-dependent kinase inhibitor 3 (CDKN3), topoisomerase II alpha (TOP2A), Aurora kinase A (AURKA) and MKI67 were identified as the candidate hub genes, which were all correlated with prostate cancer patient’ disease-free survival in TCGA. In fact, only UBE2C was highly expressed in prostate cancer when compared with benign prostate tissue in TCGA and the expression of UBE2C was also in parallel with the Gleason score of prostate cancer. Cox regression analysis has indicated UBE2C could function as the independent prognostic factor of prostate cancer. GSEA showed UBE2C had played an important role in the pathway of prostate cancer, such as NOTCH signaling pathway, WNT-β-catenin signaling pathway. CONCLUSIONS: UBE2C was pivotal for the progression of prostate cancer and the level of UBE2C was important to predict the prognosis of patients.
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spelling pubmed-79064632021-03-03 Identification of UBE2C as hub gene in driving prostate cancer by integrated bioinformatics analysis Wang, Yan Wang, Jili Tang, Qiusu Ren, Guoping PLoS One Research Article BACKGROUND: The aim of this study was to identify novel genes in promoting primary prostate cancer (PCa) progression and to explore its role in the prognosis of prostate cancer. METHODS: Four microarray datasets containing primary prostate cancer samples and benign prostate samples were downloaded from Gene Expression Omnibus (GEO), then differentially expressed genes (DEGs) were identified by R software (version 3.6.2). Gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) were performed to identify the function of DEGs. Using STRING and Cytoscape (version 3.7.1), we constructed a protein-protein interaction (PPI) network and identified the hub gene of prostate cancer. Clinical data on GSE70770 and TCGA was collected to show the role of hub gene in prostate cancer progression. The correlations between hub gene and clinical parameters were also indicated by cox regression analysis. Gene Set Enrichment Analysis (GSEA) was performed to highlight the function of Ubiquitin-conjugating enzyme complex (UBE2C) in prostate cancer. RESULTS: 243 upregulated genes and 298 downregulated genes that changed in at least two microarrays have been identified. GO and KEGG analysis indicated significant changes in the oxidation-reduction process, angiogenesis, TGF-beta signaling pathway. UBE2C, PDZ-binding kinase (PBK), cyclin B1 (CCNB1), Cyclin-dependent kinase inhibitor 3 (CDKN3), topoisomerase II alpha (TOP2A), Aurora kinase A (AURKA) and MKI67 were identified as the candidate hub genes, which were all correlated with prostate cancer patient’ disease-free survival in TCGA. In fact, only UBE2C was highly expressed in prostate cancer when compared with benign prostate tissue in TCGA and the expression of UBE2C was also in parallel with the Gleason score of prostate cancer. Cox regression analysis has indicated UBE2C could function as the independent prognostic factor of prostate cancer. GSEA showed UBE2C had played an important role in the pathway of prostate cancer, such as NOTCH signaling pathway, WNT-β-catenin signaling pathway. CONCLUSIONS: UBE2C was pivotal for the progression of prostate cancer and the level of UBE2C was important to predict the prognosis of patients. Public Library of Science 2021-02-25 /pmc/articles/PMC7906463/ /pubmed/33630978 http://dx.doi.org/10.1371/journal.pone.0247827 Text en © 2021 Wang et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Wang, Yan
Wang, Jili
Tang, Qiusu
Ren, Guoping
Identification of UBE2C as hub gene in driving prostate cancer by integrated bioinformatics analysis
title Identification of UBE2C as hub gene in driving prostate cancer by integrated bioinformatics analysis
title_full Identification of UBE2C as hub gene in driving prostate cancer by integrated bioinformatics analysis
title_fullStr Identification of UBE2C as hub gene in driving prostate cancer by integrated bioinformatics analysis
title_full_unstemmed Identification of UBE2C as hub gene in driving prostate cancer by integrated bioinformatics analysis
title_short Identification of UBE2C as hub gene in driving prostate cancer by integrated bioinformatics analysis
title_sort identification of ube2c as hub gene in driving prostate cancer by integrated bioinformatics analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7906463/
https://www.ncbi.nlm.nih.gov/pubmed/33630978
http://dx.doi.org/10.1371/journal.pone.0247827
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