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A Computational Model to Predict the Causal miRNAs for Diseases

MicroRNAs (miRNAs) are one class of important noncoding RNA molecules, and their dysfunction is associated with a number of diseases. Currently, a series of databases and algorithms have been developed for dissecting human miRNA–disease associations. However, these tools only presented the associati...

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Autores principales: Gao, Yuanxu, Jia, Kaiwen, Shi, Jiangcheng, Zhou, Yuan, Cui, Qinghua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6786093/
https://www.ncbi.nlm.nih.gov/pubmed/31632446
http://dx.doi.org/10.3389/fgene.2019.00935
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author Gao, Yuanxu
Jia, Kaiwen
Shi, Jiangcheng
Zhou, Yuan
Cui, Qinghua
author_facet Gao, Yuanxu
Jia, Kaiwen
Shi, Jiangcheng
Zhou, Yuan
Cui, Qinghua
author_sort Gao, Yuanxu
collection PubMed
description MicroRNAs (miRNAs) are one class of important noncoding RNA molecules, and their dysfunction is associated with a number of diseases. Currently, a series of databases and algorithms have been developed for dissecting human miRNA–disease associations. However, these tools only presented the associations between miRNAs and disease but did not address whether the associations are causal or not, a key biomedical issue that is critical for understanding the roles of candidate miRNAs in the mechanisms of specific diseases. Here we first manually curated causal miRNA–disease association information and updated the human miRNA disease database (HMDD) accordingly. Then we built a computational model, MDCAP (MiRNA-Disease Causal Association Predictor), to predict novel causal miRNA–disease associations. As a result, we collected 6,667 causal miRNA–disease associations between 616 miRNAs and 440 diseases, which accounts for ∼20% of the total data in HMDD. The MDCAP model achieved an area under the receiver operating characteristic (ROC) curve of 0.928 for ROC analysis by independent test and an area under the ROC curve of 0.925 for ROC analysis by 10-fold cross-validation. Finally, case studies conducted on myocardial infarction and hsa-mir-498 further suggested the biomedical significance of the predictions.
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spelling pubmed-67860932019-10-18 A Computational Model to Predict the Causal miRNAs for Diseases Gao, Yuanxu Jia, Kaiwen Shi, Jiangcheng Zhou, Yuan Cui, Qinghua Front Genet Genetics MicroRNAs (miRNAs) are one class of important noncoding RNA molecules, and their dysfunction is associated with a number of diseases. Currently, a series of databases and algorithms have been developed for dissecting human miRNA–disease associations. However, these tools only presented the associations between miRNAs and disease but did not address whether the associations are causal or not, a key biomedical issue that is critical for understanding the roles of candidate miRNAs in the mechanisms of specific diseases. Here we first manually curated causal miRNA–disease association information and updated the human miRNA disease database (HMDD) accordingly. Then we built a computational model, MDCAP (MiRNA-Disease Causal Association Predictor), to predict novel causal miRNA–disease associations. As a result, we collected 6,667 causal miRNA–disease associations between 616 miRNAs and 440 diseases, which accounts for ∼20% of the total data in HMDD. The MDCAP model achieved an area under the receiver operating characteristic (ROC) curve of 0.928 for ROC analysis by independent test and an area under the ROC curve of 0.925 for ROC analysis by 10-fold cross-validation. Finally, case studies conducted on myocardial infarction and hsa-mir-498 further suggested the biomedical significance of the predictions. Frontiers Media S.A. 2019-10-03 /pmc/articles/PMC6786093/ /pubmed/31632446 http://dx.doi.org/10.3389/fgene.2019.00935 Text en Copyright © 2019 Gao, Jia, Shi, Zhou and Cui 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
Gao, Yuanxu
Jia, Kaiwen
Shi, Jiangcheng
Zhou, Yuan
Cui, Qinghua
A Computational Model to Predict the Causal miRNAs for Diseases
title A Computational Model to Predict the Causal miRNAs for Diseases
title_full A Computational Model to Predict the Causal miRNAs for Diseases
title_fullStr A Computational Model to Predict the Causal miRNAs for Diseases
title_full_unstemmed A Computational Model to Predict the Causal miRNAs for Diseases
title_short A Computational Model to Predict the Causal miRNAs for Diseases
title_sort computational model to predict the causal mirnas for diseases
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6786093/
https://www.ncbi.nlm.nih.gov/pubmed/31632446
http://dx.doi.org/10.3389/fgene.2019.00935
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