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The gene regulatory network for breast cancer: integrated regulatory landscape of cancer hallmarks

In this study, we infer the breast cancer gene regulatory network from gene expression data. This network is obtained from the application of the BC3Net inference algorithm to a large-scale gene expression data set consisting of 351 patient samples. In order to elucidate the functional relevance of...

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Autores principales: Emmert-Streib, Frank, de Matos Simoes, Ricardo, Mullan, Paul, Haibe-Kains, Benjamin, Dehmer, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3909882/
https://www.ncbi.nlm.nih.gov/pubmed/24550935
http://dx.doi.org/10.3389/fgene.2014.00015
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author Emmert-Streib, Frank
de Matos Simoes, Ricardo
Mullan, Paul
Haibe-Kains, Benjamin
Dehmer, Matthias
author_facet Emmert-Streib, Frank
de Matos Simoes, Ricardo
Mullan, Paul
Haibe-Kains, Benjamin
Dehmer, Matthias
author_sort Emmert-Streib, Frank
collection PubMed
description In this study, we infer the breast cancer gene regulatory network from gene expression data. This network is obtained from the application of the BC3Net inference algorithm to a large-scale gene expression data set consisting of 351 patient samples. In order to elucidate the functional relevance of the inferred network, we are performing a Gene Ontology (GO) analysis for its structural components. Our analysis reveals that most significant GO-terms we find for the breast cancer network represent functional modules of biological processes that are described by known cancer hallmarks, including translation, immune response, cell cycle, organelle fission, mitosis, cell adhesion, RNA processing, RNA splicing and response to wounding. Furthermore, by using a curated list of census cancer genes, we find an enrichment in these functional modules. Finally, we study cooperative effects of chromosomes based on information of interacting genes in the beast cancer network. We find that chromosome 21 is most coactive with other chromosomes. To our knowledge this is the first study investigating the genome-scale breast cancer network.
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spelling pubmed-39098822014-02-18 The gene regulatory network for breast cancer: integrated regulatory landscape of cancer hallmarks Emmert-Streib, Frank de Matos Simoes, Ricardo Mullan, Paul Haibe-Kains, Benjamin Dehmer, Matthias Front Genet Genetics In this study, we infer the breast cancer gene regulatory network from gene expression data. This network is obtained from the application of the BC3Net inference algorithm to a large-scale gene expression data set consisting of 351 patient samples. In order to elucidate the functional relevance of the inferred network, we are performing a Gene Ontology (GO) analysis for its structural components. Our analysis reveals that most significant GO-terms we find for the breast cancer network represent functional modules of biological processes that are described by known cancer hallmarks, including translation, immune response, cell cycle, organelle fission, mitosis, cell adhesion, RNA processing, RNA splicing and response to wounding. Furthermore, by using a curated list of census cancer genes, we find an enrichment in these functional modules. Finally, we study cooperative effects of chromosomes based on information of interacting genes in the beast cancer network. We find that chromosome 21 is most coactive with other chromosomes. To our knowledge this is the first study investigating the genome-scale breast cancer network. Frontiers Media S.A. 2014-02-03 /pmc/articles/PMC3909882/ /pubmed/24550935 http://dx.doi.org/10.3389/fgene.2014.00015 Text en Copyright © 2014 Emmert-Streib, de Matos Simoes, Mullan, Haibe-Kains and Dehmer. http://creativecommons.org/licenses/by/3.0/ 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) or licensor 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 Genetics
Emmert-Streib, Frank
de Matos Simoes, Ricardo
Mullan, Paul
Haibe-Kains, Benjamin
Dehmer, Matthias
The gene regulatory network for breast cancer: integrated regulatory landscape of cancer hallmarks
title The gene regulatory network for breast cancer: integrated regulatory landscape of cancer hallmarks
title_full The gene regulatory network for breast cancer: integrated regulatory landscape of cancer hallmarks
title_fullStr The gene regulatory network for breast cancer: integrated regulatory landscape of cancer hallmarks
title_full_unstemmed The gene regulatory network for breast cancer: integrated regulatory landscape of cancer hallmarks
title_short The gene regulatory network for breast cancer: integrated regulatory landscape of cancer hallmarks
title_sort gene regulatory network for breast cancer: integrated regulatory landscape of cancer hallmarks
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3909882/
https://www.ncbi.nlm.nih.gov/pubmed/24550935
http://dx.doi.org/10.3389/fgene.2014.00015
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