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miRDDCR: a miRNA-based method to comprehensively infer drug-disease causal relationships
Revealing the cause-and-effect mechanism behind drug-disease relationships remains a challenging task. Recent studies suggested that drugs can target microRNAs (miRNAs) and alter their expression levels. In the meanwhile, the inappropriate expression of miRNAs will lead to various diseases. Therefor...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5698443/ https://www.ncbi.nlm.nih.gov/pubmed/29162848 http://dx.doi.org/10.1038/s41598-017-15716-8 |
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author | Chen, Hailin Zhang, Zuping Peng, Wei |
author_facet | Chen, Hailin Zhang, Zuping Peng, Wei |
author_sort | Chen, Hailin |
collection | PubMed |
description | Revealing the cause-and-effect mechanism behind drug-disease relationships remains a challenging task. Recent studies suggested that drugs can target microRNAs (miRNAs) and alter their expression levels. In the meanwhile, the inappropriate expression of miRNAs will lead to various diseases. Therefore, targeting specific miRNAs by small-molecule drugs to modulate their activities provides a promising approach to human disease treatment. However, few studies attempt to discover drug-disease causal relationships through the molecular level of miRNAs. Here, we developed a miRNA-based inference method miRDDCR to comprehensively predict drug-disease causal relationships. We first constructed a three-layer drug-miRNA-disease heterogeneous network by combining similarity measurements, existing drug-miRNA associations and miRNA-disease associations. Then, we extended the algorithm of Random Walk to the three-layer heterogeneous network and ranked the potential indications for drugs. Leave-one-out cross-validations and case studies demonstrated that our method miRDDCR can achieve excellent prediction power. Compared with related methods, our causality discovery-based algorithm showed superior prediction ability and highlighted the molecular basis miRNAs, which can be used to assist in the experimental design for drug development and disease treatment. Finally, comprehensively inferred drug-disease causal relationships were released for further studies. |
format | Online Article Text |
id | pubmed-5698443 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56984432017-11-29 miRDDCR: a miRNA-based method to comprehensively infer drug-disease causal relationships Chen, Hailin Zhang, Zuping Peng, Wei Sci Rep Article Revealing the cause-and-effect mechanism behind drug-disease relationships remains a challenging task. Recent studies suggested that drugs can target microRNAs (miRNAs) and alter their expression levels. In the meanwhile, the inappropriate expression of miRNAs will lead to various diseases. Therefore, targeting specific miRNAs by small-molecule drugs to modulate their activities provides a promising approach to human disease treatment. However, few studies attempt to discover drug-disease causal relationships through the molecular level of miRNAs. Here, we developed a miRNA-based inference method miRDDCR to comprehensively predict drug-disease causal relationships. We first constructed a three-layer drug-miRNA-disease heterogeneous network by combining similarity measurements, existing drug-miRNA associations and miRNA-disease associations. Then, we extended the algorithm of Random Walk to the three-layer heterogeneous network and ranked the potential indications for drugs. Leave-one-out cross-validations and case studies demonstrated that our method miRDDCR can achieve excellent prediction power. Compared with related methods, our causality discovery-based algorithm showed superior prediction ability and highlighted the molecular basis miRNAs, which can be used to assist in the experimental design for drug development and disease treatment. Finally, comprehensively inferred drug-disease causal relationships were released for further studies. Nature Publishing Group UK 2017-11-21 /pmc/articles/PMC5698443/ /pubmed/29162848 http://dx.doi.org/10.1038/s41598-017-15716-8 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Chen, Hailin Zhang, Zuping Peng, Wei miRDDCR: a miRNA-based method to comprehensively infer drug-disease causal relationships |
title | miRDDCR: a miRNA-based method to comprehensively infer drug-disease causal relationships |
title_full | miRDDCR: a miRNA-based method to comprehensively infer drug-disease causal relationships |
title_fullStr | miRDDCR: a miRNA-based method to comprehensively infer drug-disease causal relationships |
title_full_unstemmed | miRDDCR: a miRNA-based method to comprehensively infer drug-disease causal relationships |
title_short | miRDDCR: a miRNA-based method to comprehensively infer drug-disease causal relationships |
title_sort | mirddcr: a mirna-based method to comprehensively infer drug-disease causal relationships |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5698443/ https://www.ncbi.nlm.nih.gov/pubmed/29162848 http://dx.doi.org/10.1038/s41598-017-15716-8 |
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