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Integrated bioinformatics analysis to identify 15 hub genes in breast cancer

The aim of the present study was to identify the hub genes and provide insight into the tumorigenesis and development of breast cancer. To examine the hub genes in breast cancer, integrated bioinformatics analysis was performed. Gene expression profiles were obtained from the Gene Expression Omnibus...

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Autores principales: Jin, Haoxuan, Huang, Xiaoyan, Shao, Kang, Li, Guibo, Wang, Jian, Yang, Huanming, Hou, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6607081/
https://www.ncbi.nlm.nih.gov/pubmed/31423162
http://dx.doi.org/10.3892/ol.2019.10411
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author Jin, Haoxuan
Huang, Xiaoyan
Shao, Kang
Li, Guibo
Wang, Jian
Yang, Huanming
Hou, Yong
author_facet Jin, Haoxuan
Huang, Xiaoyan
Shao, Kang
Li, Guibo
Wang, Jian
Yang, Huanming
Hou, Yong
author_sort Jin, Haoxuan
collection PubMed
description The aim of the present study was to identify the hub genes and provide insight into the tumorigenesis and development of breast cancer. To examine the hub genes in breast cancer, integrated bioinformatics analysis was performed. Gene expression profiles were obtained from the Gene Expression Omnibus (GEO) database and the differentially expressed genes (DEGs) were identified using the ‘limma’ package in R. Gene Ontology enrichment analysis and Kyoto Encyclopedia of Genes and Genomes pathway analysis was used to determine the functional annotations and potential pathways of the DEGs. Subsequently, a protein-protein interaction network analysis and weighted correlation network analysis (WGCNA) were conducted to identify hub genes. To confirm the reliability of the identified hub genes, RNA gene expression profiles were obtained from The Cancer Genome Atlas (TCGA)-breast cancer database, and WGCNA was used to screen for genes that were markedly correlated with breast cancer. By combining the results from the GEO and TCGA datasets, 15 hub genes were identified to be associated with breast cancer pathophysiology. Overall survival analysis was performed to examine the association between the expression of hub genes and the overall survival time of patients with breast cancer. Higher expression of all hub genes was associated with significantly shorter overall survival in patients with breast cancer compared with patients with lower levels of expression of the respective gene.
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spelling pubmed-66070812019-08-18 Integrated bioinformatics analysis to identify 15 hub genes in breast cancer Jin, Haoxuan Huang, Xiaoyan Shao, Kang Li, Guibo Wang, Jian Yang, Huanming Hou, Yong Oncol Lett Articles The aim of the present study was to identify the hub genes and provide insight into the tumorigenesis and development of breast cancer. To examine the hub genes in breast cancer, integrated bioinformatics analysis was performed. Gene expression profiles were obtained from the Gene Expression Omnibus (GEO) database and the differentially expressed genes (DEGs) were identified using the ‘limma’ package in R. Gene Ontology enrichment analysis and Kyoto Encyclopedia of Genes and Genomes pathway analysis was used to determine the functional annotations and potential pathways of the DEGs. Subsequently, a protein-protein interaction network analysis and weighted correlation network analysis (WGCNA) were conducted to identify hub genes. To confirm the reliability of the identified hub genes, RNA gene expression profiles were obtained from The Cancer Genome Atlas (TCGA)-breast cancer database, and WGCNA was used to screen for genes that were markedly correlated with breast cancer. By combining the results from the GEO and TCGA datasets, 15 hub genes were identified to be associated with breast cancer pathophysiology. Overall survival analysis was performed to examine the association between the expression of hub genes and the overall survival time of patients with breast cancer. Higher expression of all hub genes was associated with significantly shorter overall survival in patients with breast cancer compared with patients with lower levels of expression of the respective gene. D.A. Spandidos 2019-08 2019-05-30 /pmc/articles/PMC6607081/ /pubmed/31423162 http://dx.doi.org/10.3892/ol.2019.10411 Text en Copyright: © Jin et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Jin, Haoxuan
Huang, Xiaoyan
Shao, Kang
Li, Guibo
Wang, Jian
Yang, Huanming
Hou, Yong
Integrated bioinformatics analysis to identify 15 hub genes in breast cancer
title Integrated bioinformatics analysis to identify 15 hub genes in breast cancer
title_full Integrated bioinformatics analysis to identify 15 hub genes in breast cancer
title_fullStr Integrated bioinformatics analysis to identify 15 hub genes in breast cancer
title_full_unstemmed Integrated bioinformatics analysis to identify 15 hub genes in breast cancer
title_short Integrated bioinformatics analysis to identify 15 hub genes in breast cancer
title_sort integrated bioinformatics analysis to identify 15 hub genes in breast cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6607081/
https://www.ncbi.nlm.nih.gov/pubmed/31423162
http://dx.doi.org/10.3892/ol.2019.10411
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