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Overexpression of ASPM, CDC20, and TTK Confer a Poorer Prognosis in Breast Cancer Identified by Gene Co-expression Network Analysis

Breast cancer is one of the most common malignancies among females, and its prognosis is affected by a complex network of gene interactions. In this study, we constructed free-scale gene co-expression networks using weighted gene co-expression network analysis (WGCNA). The gene expression profiles o...

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Autores principales: Tang, Jianing, Lu, Mengxin, Cui, Qiuxia, Zhang, Dan, Kong, Deguang, Liao, Xing, Ren, Jiangbo, Gong, Yan, Wu, Gaosong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6492458/
https://www.ncbi.nlm.nih.gov/pubmed/31106147
http://dx.doi.org/10.3389/fonc.2019.00310
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author Tang, Jianing
Lu, Mengxin
Cui, Qiuxia
Zhang, Dan
Kong, Deguang
Liao, Xing
Ren, Jiangbo
Gong, Yan
Wu, Gaosong
author_facet Tang, Jianing
Lu, Mengxin
Cui, Qiuxia
Zhang, Dan
Kong, Deguang
Liao, Xing
Ren, Jiangbo
Gong, Yan
Wu, Gaosong
author_sort Tang, Jianing
collection PubMed
description Breast cancer is one of the most common malignancies among females, and its prognosis is affected by a complex network of gene interactions. In this study, we constructed free-scale gene co-expression networks using weighted gene co-expression network analysis (WGCNA). The gene expression profiles of GSE25055 were downloaded from the Gene Expression Omnibus (GEO) database to identify potential biomarkers associated with breast cancer progression. GSE42568 was downloaded for validation. A total of 9 modules were established via the average linkage hierarchical clustering. We identified 3 hub genes (ASPM, CDC20, and TTK) in the significant module (R(2) = 0.52), which were significantly correlated with poor prognosis both in test and validation datasets. In the datasets GSE25055 and GSE42568, higher expression levels of ASPM, CDC20, and TTK correlated with advanced tumor grades. Immunohistochemistry data from the Human Protein Atlas also demonstrated that their protein levels were higher in tumor samples. According to gene set enrichment analysis, 4 commonly enriched pathways were identified: cell cycle pathway, DNA replication pathway, homologous recombination pathway, and P53 signaling pathway. In addition, strong correlations were found among their expression levels. In conclusion, our WGCNA analysis identified candidate prognostic biomarkers for further basic and clinical researches.
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spelling pubmed-64924582019-05-17 Overexpression of ASPM, CDC20, and TTK Confer a Poorer Prognosis in Breast Cancer Identified by Gene Co-expression Network Analysis Tang, Jianing Lu, Mengxin Cui, Qiuxia Zhang, Dan Kong, Deguang Liao, Xing Ren, Jiangbo Gong, Yan Wu, Gaosong Front Oncol Oncology Breast cancer is one of the most common malignancies among females, and its prognosis is affected by a complex network of gene interactions. In this study, we constructed free-scale gene co-expression networks using weighted gene co-expression network analysis (WGCNA). The gene expression profiles of GSE25055 were downloaded from the Gene Expression Omnibus (GEO) database to identify potential biomarkers associated with breast cancer progression. GSE42568 was downloaded for validation. A total of 9 modules were established via the average linkage hierarchical clustering. We identified 3 hub genes (ASPM, CDC20, and TTK) in the significant module (R(2) = 0.52), which were significantly correlated with poor prognosis both in test and validation datasets. In the datasets GSE25055 and GSE42568, higher expression levels of ASPM, CDC20, and TTK correlated with advanced tumor grades. Immunohistochemistry data from the Human Protein Atlas also demonstrated that their protein levels were higher in tumor samples. According to gene set enrichment analysis, 4 commonly enriched pathways were identified: cell cycle pathway, DNA replication pathway, homologous recombination pathway, and P53 signaling pathway. In addition, strong correlations were found among their expression levels. In conclusion, our WGCNA analysis identified candidate prognostic biomarkers for further basic and clinical researches. Frontiers Media S.A. 2019-04-24 /pmc/articles/PMC6492458/ /pubmed/31106147 http://dx.doi.org/10.3389/fonc.2019.00310 Text en Copyright © 2019 Tang, Lu, Cui, Zhang, Kong, Liao, Ren, Gong and Wu. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Tang, Jianing
Lu, Mengxin
Cui, Qiuxia
Zhang, Dan
Kong, Deguang
Liao, Xing
Ren, Jiangbo
Gong, Yan
Wu, Gaosong
Overexpression of ASPM, CDC20, and TTK Confer a Poorer Prognosis in Breast Cancer Identified by Gene Co-expression Network Analysis
title Overexpression of ASPM, CDC20, and TTK Confer a Poorer Prognosis in Breast Cancer Identified by Gene Co-expression Network Analysis
title_full Overexpression of ASPM, CDC20, and TTK Confer a Poorer Prognosis in Breast Cancer Identified by Gene Co-expression Network Analysis
title_fullStr Overexpression of ASPM, CDC20, and TTK Confer a Poorer Prognosis in Breast Cancer Identified by Gene Co-expression Network Analysis
title_full_unstemmed Overexpression of ASPM, CDC20, and TTK Confer a Poorer Prognosis in Breast Cancer Identified by Gene Co-expression Network Analysis
title_short Overexpression of ASPM, CDC20, and TTK Confer a Poorer Prognosis in Breast Cancer Identified by Gene Co-expression Network Analysis
title_sort overexpression of aspm, cdc20, and ttk confer a poorer prognosis in breast cancer identified by gene co-expression network analysis
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6492458/
https://www.ncbi.nlm.nih.gov/pubmed/31106147
http://dx.doi.org/10.3389/fonc.2019.00310
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