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Master Regulators of Signaling Pathways: An Application to the Analysis of Gene Regulation in Breast Cancer

Analysis of gene regulatory networks allows the identification of master transcriptional factors that control specific groups of genes. In this work, we inferred a gene regulatory network from a large dataset of breast cancer samples to identify the master transcriptional factors that control the ge...

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Autores principales: Tapia-Carrillo, Diana, Tovar, Hugo, Velazquez-Caldelas, Tadeo Enrique, Hernandez-Lemus, Enrique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6902642/
https://www.ncbi.nlm.nih.gov/pubmed/31850059
http://dx.doi.org/10.3389/fgene.2019.01180
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author Tapia-Carrillo, Diana
Tovar, Hugo
Velazquez-Caldelas, Tadeo Enrique
Hernandez-Lemus, Enrique
author_facet Tapia-Carrillo, Diana
Tovar, Hugo
Velazquez-Caldelas, Tadeo Enrique
Hernandez-Lemus, Enrique
author_sort Tapia-Carrillo, Diana
collection PubMed
description Analysis of gene regulatory networks allows the identification of master transcriptional factors that control specific groups of genes. In this work, we inferred a gene regulatory network from a large dataset of breast cancer samples to identify the master transcriptional factors that control the genes within signal transduction pathways. The focus in a particular subset of relevant genes constitutes an extension of the original Master Regulator Inference Algorithm (MARINa) analysis. This modified version of MARINa utilizes a restricted molecular signature containing genes from the 25 human pathways in KEGG's signal transduction category. Our breast cancer RNAseq expression dataset consists of 881 samples comprising tumors and normal mammary gland tissue. The top 10 master transcriptional factors found to regulate signal transduction pathways in breast cancer we identified are: TSHZ2, HOXA2, MEIS2, HOXA3, HAND2, HOXA5, TBX18, PEG3, GLI2, and CLOCK. The functional enrichment of the regulons of these master transcriptional factors showed an important proportion of processes related to morphogenesis. Our results suggest that, as part of the aberrant regulation of signaling pathways in breast cancer, pathways similar to the regulation of cell differentiation, cardiovascular system development, and vasculature development may be dysregulated and co-opted in favor of tumor development through the action of these transcription factors.
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spelling pubmed-69026422019-12-17 Master Regulators of Signaling Pathways: An Application to the Analysis of Gene Regulation in Breast Cancer Tapia-Carrillo, Diana Tovar, Hugo Velazquez-Caldelas, Tadeo Enrique Hernandez-Lemus, Enrique Front Genet Genetics Analysis of gene regulatory networks allows the identification of master transcriptional factors that control specific groups of genes. In this work, we inferred a gene regulatory network from a large dataset of breast cancer samples to identify the master transcriptional factors that control the genes within signal transduction pathways. The focus in a particular subset of relevant genes constitutes an extension of the original Master Regulator Inference Algorithm (MARINa) analysis. This modified version of MARINa utilizes a restricted molecular signature containing genes from the 25 human pathways in KEGG's signal transduction category. Our breast cancer RNAseq expression dataset consists of 881 samples comprising tumors and normal mammary gland tissue. The top 10 master transcriptional factors found to regulate signal transduction pathways in breast cancer we identified are: TSHZ2, HOXA2, MEIS2, HOXA3, HAND2, HOXA5, TBX18, PEG3, GLI2, and CLOCK. The functional enrichment of the regulons of these master transcriptional factors showed an important proportion of processes related to morphogenesis. Our results suggest that, as part of the aberrant regulation of signaling pathways in breast cancer, pathways similar to the regulation of cell differentiation, cardiovascular system development, and vasculature development may be dysregulated and co-opted in favor of tumor development through the action of these transcription factors. Frontiers Media S.A. 2019-12-03 /pmc/articles/PMC6902642/ /pubmed/31850059 http://dx.doi.org/10.3389/fgene.2019.01180 Text en Copyright © 2019 Tapia-Carrillo, Tovar, Velazquez-Caldelas and Hernandez-Lemus 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 Genetics
Tapia-Carrillo, Diana
Tovar, Hugo
Velazquez-Caldelas, Tadeo Enrique
Hernandez-Lemus, Enrique
Master Regulators of Signaling Pathways: An Application to the Analysis of Gene Regulation in Breast Cancer
title Master Regulators of Signaling Pathways: An Application to the Analysis of Gene Regulation in Breast Cancer
title_full Master Regulators of Signaling Pathways: An Application to the Analysis of Gene Regulation in Breast Cancer
title_fullStr Master Regulators of Signaling Pathways: An Application to the Analysis of Gene Regulation in Breast Cancer
title_full_unstemmed Master Regulators of Signaling Pathways: An Application to the Analysis of Gene Regulation in Breast Cancer
title_short Master Regulators of Signaling Pathways: An Application to the Analysis of Gene Regulation in Breast Cancer
title_sort master regulators of signaling pathways: an application to the analysis of gene regulation in breast cancer
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6902642/
https://www.ncbi.nlm.nih.gov/pubmed/31850059
http://dx.doi.org/10.3389/fgene.2019.01180
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