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Identification of active miRNA and transcription factor regulatory pathways in human obesity-related inflammation

BACKGROUND: Obesity-induced chronic inflammation plays a fundamental role in the pathogenesis of metabolic syndrome (MS). Recently, a growing body of evidence supports that miRNAs are largely dysregulated in obesity and that specific miRNAs regulate obesity-associated inflammation. We applied an app...

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Autores principales: Zhang, Xi-Mei, Guo, Lin, Chi, Mei-Hua, Sun, Hong-Mei, Chen, Xiao-Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4355475/
https://www.ncbi.nlm.nih.gov/pubmed/25887648
http://dx.doi.org/10.1186/s12859-015-0512-5
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author Zhang, Xi-Mei
Guo, Lin
Chi, Mei-Hua
Sun, Hong-Mei
Chen, Xiao-Wen
author_facet Zhang, Xi-Mei
Guo, Lin
Chi, Mei-Hua
Sun, Hong-Mei
Chen, Xiao-Wen
author_sort Zhang, Xi-Mei
collection PubMed
description BACKGROUND: Obesity-induced chronic inflammation plays a fundamental role in the pathogenesis of metabolic syndrome (MS). Recently, a growing body of evidence supports that miRNAs are largely dysregulated in obesity and that specific miRNAs regulate obesity-associated inflammation. We applied an approach aiming to identify active miRNA-TF-gene regulatory pathways in obesity. Firstly, we detected differentially expressed genes (DEGs) and differentially expressed miRNAs (DEmiRs) from mRNA and miRNA expression profiles, respectively. Secondly, by mapping the DEGs and DEmiRs to the curated miRNA-TF-gene regulatory network as active seed nodes and connect them with their immediate neighbors, we obtained the potential active miRNA-TF-gene regulatory subnetwork in obesity. Thirdly, using a Breadth-First-Search (BFS) algorithm, we identified potential active miRNA-TF-gene regulatory pathways in obesity. Finally, through the hypergeometric test, we identified the active miRNA-TF-gene regulatory pathways that were significantly related to obesity. RESULTS: The potential active pathways with FDR < 0.0005 were considered to be the active miRNA-TF regulatory pathways in obesity. The union of the active pathways is visualized and identical nodes of the active pathways were merged. CONCLUSIONS: We identified 23 active miRNA-TF-gene regulatory pathways that were significantly related to obesity-related inflammation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-015-0512-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-43554752015-03-12 Identification of active miRNA and transcription factor regulatory pathways in human obesity-related inflammation Zhang, Xi-Mei Guo, Lin Chi, Mei-Hua Sun, Hong-Mei Chen, Xiao-Wen BMC Bioinformatics Research Article BACKGROUND: Obesity-induced chronic inflammation plays a fundamental role in the pathogenesis of metabolic syndrome (MS). Recently, a growing body of evidence supports that miRNAs are largely dysregulated in obesity and that specific miRNAs regulate obesity-associated inflammation. We applied an approach aiming to identify active miRNA-TF-gene regulatory pathways in obesity. Firstly, we detected differentially expressed genes (DEGs) and differentially expressed miRNAs (DEmiRs) from mRNA and miRNA expression profiles, respectively. Secondly, by mapping the DEGs and DEmiRs to the curated miRNA-TF-gene regulatory network as active seed nodes and connect them with their immediate neighbors, we obtained the potential active miRNA-TF-gene regulatory subnetwork in obesity. Thirdly, using a Breadth-First-Search (BFS) algorithm, we identified potential active miRNA-TF-gene regulatory pathways in obesity. Finally, through the hypergeometric test, we identified the active miRNA-TF-gene regulatory pathways that were significantly related to obesity. RESULTS: The potential active pathways with FDR < 0.0005 were considered to be the active miRNA-TF regulatory pathways in obesity. The union of the active pathways is visualized and identical nodes of the active pathways were merged. CONCLUSIONS: We identified 23 active miRNA-TF-gene regulatory pathways that were significantly related to obesity-related inflammation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-015-0512-5) contains supplementary material, which is available to authorized users. BioMed Central 2015-03-07 /pmc/articles/PMC4355475/ /pubmed/25887648 http://dx.doi.org/10.1186/s12859-015-0512-5 Text en © Zhang et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Article
Zhang, Xi-Mei
Guo, Lin
Chi, Mei-Hua
Sun, Hong-Mei
Chen, Xiao-Wen
Identification of active miRNA and transcription factor regulatory pathways in human obesity-related inflammation
title Identification of active miRNA and transcription factor regulatory pathways in human obesity-related inflammation
title_full Identification of active miRNA and transcription factor regulatory pathways in human obesity-related inflammation
title_fullStr Identification of active miRNA and transcription factor regulatory pathways in human obesity-related inflammation
title_full_unstemmed Identification of active miRNA and transcription factor regulatory pathways in human obesity-related inflammation
title_short Identification of active miRNA and transcription factor regulatory pathways in human obesity-related inflammation
title_sort identification of active mirna and transcription factor regulatory pathways in human obesity-related inflammation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4355475/
https://www.ncbi.nlm.nih.gov/pubmed/25887648
http://dx.doi.org/10.1186/s12859-015-0512-5
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