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Comparisons of gene coexpression network modules in breast cancer and ovarian cancer

BACKGROUND: Breast cancer and ovarian cancer are hormone driven and are known to have some predisposition genes in common such as the two well known cancer genes BRCA1 and BRCA2. The objective of this study is to compare the coexpression network modules of both cancers, so as to infer the potential...

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Autor principal: Zhang, Shuqin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5907153/
https://www.ncbi.nlm.nih.gov/pubmed/29671401
http://dx.doi.org/10.1186/s12918-018-0530-9
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author Zhang, Shuqin
author_facet Zhang, Shuqin
author_sort Zhang, Shuqin
collection PubMed
description BACKGROUND: Breast cancer and ovarian cancer are hormone driven and are known to have some predisposition genes in common such as the two well known cancer genes BRCA1 and BRCA2. The objective of this study is to compare the coexpression network modules of both cancers, so as to infer the potential cancer-related modules. METHODS: We applied the eigen-decomposition to the matrix that integrates the gene coexpression networks of both breast cancer and ovarian cancer. With hierarchical clustering of the related eigenvectors, we obtained the network modules of both cancers simultaneously. Enrichment analysis on Gene Ontology (GO), KEGG pathway, Disease Ontology (DO), and Gene Set Enrichment Analysis (GSEA) in the identified modules was performed. RESULTS: We identified 43 modules that are enriched by at least one of the four types of enrichments. 31, 25, and 18 modules are enriched by GO terms, KEGG pathways, and DO terms, respectively. The structure of 29 modules in both cancers is significantly different with p-values less than 0.05, of which 25 modules have larger densities in ovarian cancer. One module was found to be significantly enriched by the terms related to breast cancer from GO, KEGG and DO enrichment. One module was found to be significantly enriched by ovarian cancer related terms. CONCLUSION: Breast cancer and ovarian cancer share some common properties on the module level. Integration of both cancers helps identifying the potential cancer associated modules. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12918-018-0530-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-59071532018-04-30 Comparisons of gene coexpression network modules in breast cancer and ovarian cancer Zhang, Shuqin BMC Syst Biol Research BACKGROUND: Breast cancer and ovarian cancer are hormone driven and are known to have some predisposition genes in common such as the two well known cancer genes BRCA1 and BRCA2. The objective of this study is to compare the coexpression network modules of both cancers, so as to infer the potential cancer-related modules. METHODS: We applied the eigen-decomposition to the matrix that integrates the gene coexpression networks of both breast cancer and ovarian cancer. With hierarchical clustering of the related eigenvectors, we obtained the network modules of both cancers simultaneously. Enrichment analysis on Gene Ontology (GO), KEGG pathway, Disease Ontology (DO), and Gene Set Enrichment Analysis (GSEA) in the identified modules was performed. RESULTS: We identified 43 modules that are enriched by at least one of the four types of enrichments. 31, 25, and 18 modules are enriched by GO terms, KEGG pathways, and DO terms, respectively. The structure of 29 modules in both cancers is significantly different with p-values less than 0.05, of which 25 modules have larger densities in ovarian cancer. One module was found to be significantly enriched by the terms related to breast cancer from GO, KEGG and DO enrichment. One module was found to be significantly enriched by ovarian cancer related terms. CONCLUSION: Breast cancer and ovarian cancer share some common properties on the module level. Integration of both cancers helps identifying the potential cancer associated modules. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12918-018-0530-9) contains supplementary material, which is available to authorized users. BioMed Central 2018-04-11 /pmc/articles/PMC5907153/ /pubmed/29671401 http://dx.doi.org/10.1186/s12918-018-0530-9 Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Zhang, Shuqin
Comparisons of gene coexpression network modules in breast cancer and ovarian cancer
title Comparisons of gene coexpression network modules in breast cancer and ovarian cancer
title_full Comparisons of gene coexpression network modules in breast cancer and ovarian cancer
title_fullStr Comparisons of gene coexpression network modules in breast cancer and ovarian cancer
title_full_unstemmed Comparisons of gene coexpression network modules in breast cancer and ovarian cancer
title_short Comparisons of gene coexpression network modules in breast cancer and ovarian cancer
title_sort comparisons of gene coexpression network modules in breast cancer and ovarian cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5907153/
https://www.ncbi.nlm.nih.gov/pubmed/29671401
http://dx.doi.org/10.1186/s12918-018-0530-9
work_keys_str_mv AT zhangshuqin comparisonsofgenecoexpressionnetworkmodulesinbreastcancerandovariancancer