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Discovery of inflammatory bowel disease-associated miRNAs using a novel bipartite clustering approach

BACKGROUND: Multidimensional data mining from an integrated environment of different data sources is frequently performed in computational system biology. The molecular mechanism from the analysis of a complex network of gene-miRNA can aid to diagnosis and treatment of associated diseases. METHODS:...

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Autores principales: Altaf-Ul-Amin, Md., Karim, Mohammad Bozlul, Hu, Pingzhao, ONO, Naoaki, Kanaya, Shigehiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7038528/
https://www.ncbi.nlm.nih.gov/pubmed/32093721
http://dx.doi.org/10.1186/s12920-020-0660-y
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author Altaf-Ul-Amin, Md.
Karim, Mohammad Bozlul
Hu, Pingzhao
ONO, Naoaki
Kanaya, Shigehiko
author_facet Altaf-Ul-Amin, Md.
Karim, Mohammad Bozlul
Hu, Pingzhao
ONO, Naoaki
Kanaya, Shigehiko
author_sort Altaf-Ul-Amin, Md.
collection PubMed
description BACKGROUND: Multidimensional data mining from an integrated environment of different data sources is frequently performed in computational system biology. The molecular mechanism from the analysis of a complex network of gene-miRNA can aid to diagnosis and treatment of associated diseases. METHODS: In this work, we mainly focus on finding inflammatory bowel disease (IBD) associated microRNAs (miRNAs) by biclustering the miRNA-target interactions aided by known IBD risk genes and their associated miRNAs collected from several sources. We rank different miRNAs by attributing to the dataset size and connectivity of IBD associated genes in the miRNA regulatory modules from biclusters. We search the association of some top-ranking miRNAs to IBD related diseases. We also search the network of discovered miRNAs to different diseases and evaluate the similarity of those diseases to IBD. RESULTS: According to different literature, our results show the significance of top-ranking miRNA to IBD or related diseases. The ratio analysis supports our ranking method where the top 20 miRNA has approximately tenfold attachment to IBD genes. From disease-associated miRNA network analysis we found that 71% of different diseases attached to those miRNAs show more than 0.75 similarity scores to IBD. CONCLUSION: We successfully identify some miRNAs related to IBD where the scoring formula and disease-associated network analysis show the significance of our method. This method can be a promising approach for isolating miRNAs for similar types of diseases.
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spelling pubmed-70385282020-03-02 Discovery of inflammatory bowel disease-associated miRNAs using a novel bipartite clustering approach Altaf-Ul-Amin, Md. Karim, Mohammad Bozlul Hu, Pingzhao ONO, Naoaki Kanaya, Shigehiko BMC Med Genomics Research BACKGROUND: Multidimensional data mining from an integrated environment of different data sources is frequently performed in computational system biology. The molecular mechanism from the analysis of a complex network of gene-miRNA can aid to diagnosis and treatment of associated diseases. METHODS: In this work, we mainly focus on finding inflammatory bowel disease (IBD) associated microRNAs (miRNAs) by biclustering the miRNA-target interactions aided by known IBD risk genes and their associated miRNAs collected from several sources. We rank different miRNAs by attributing to the dataset size and connectivity of IBD associated genes in the miRNA regulatory modules from biclusters. We search the association of some top-ranking miRNAs to IBD related diseases. We also search the network of discovered miRNAs to different diseases and evaluate the similarity of those diseases to IBD. RESULTS: According to different literature, our results show the significance of top-ranking miRNA to IBD or related diseases. The ratio analysis supports our ranking method where the top 20 miRNA has approximately tenfold attachment to IBD genes. From disease-associated miRNA network analysis we found that 71% of different diseases attached to those miRNAs show more than 0.75 similarity scores to IBD. CONCLUSION: We successfully identify some miRNAs related to IBD where the scoring formula and disease-associated network analysis show the significance of our method. This method can be a promising approach for isolating miRNAs for similar types of diseases. BioMed Central 2020-02-24 /pmc/articles/PMC7038528/ /pubmed/32093721 http://dx.doi.org/10.1186/s12920-020-0660-y Text en © The Author(s) 2020 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
Altaf-Ul-Amin, Md.
Karim, Mohammad Bozlul
Hu, Pingzhao
ONO, Naoaki
Kanaya, Shigehiko
Discovery of inflammatory bowel disease-associated miRNAs using a novel bipartite clustering approach
title Discovery of inflammatory bowel disease-associated miRNAs using a novel bipartite clustering approach
title_full Discovery of inflammatory bowel disease-associated miRNAs using a novel bipartite clustering approach
title_fullStr Discovery of inflammatory bowel disease-associated miRNAs using a novel bipartite clustering approach
title_full_unstemmed Discovery of inflammatory bowel disease-associated miRNAs using a novel bipartite clustering approach
title_short Discovery of inflammatory bowel disease-associated miRNAs using a novel bipartite clustering approach
title_sort discovery of inflammatory bowel disease-associated mirnas using a novel bipartite clustering approach
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7038528/
https://www.ncbi.nlm.nih.gov/pubmed/32093721
http://dx.doi.org/10.1186/s12920-020-0660-y
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