A Novel Approach Based on a Weighted Interactive Network to Predict Associations of MiRNAs and Diseases

Accumulating evidence progressively indicated that microRNAs (miRNAs) play a significant role in the pathogenesis of diseases through many experimental studies; therefore, developing powerful computational models to identify potential human miRNA–disease associations is vital for an understanding of...

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Main Authors: Haochen Zhao, Linai Kuang, Xiang Feng, Quan Zou, Lei Wang
Format: Article
Language:English
Published: MDPI AG 2018-12-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:http://www.mdpi.com/1422-0067/20/1/110
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spelling doaj-aea06b89ecd3493588eee670c3927f282020-11-24T22:00:03ZengMDPI AGInternational Journal of Molecular Sciences1422-00672018-12-0120111010.3390/ijms20010110ijms20010110A Novel Approach Based on a Weighted Interactive Network to Predict Associations of MiRNAs and DiseasesHaochen Zhao0Linai Kuang1Xiang Feng2Quan Zou3Lei Wang4Key Laboratory of Hunan Province for Internet of Things and Information Security, Xiangtan University, Xiangtan 411105, ChinaCollege of Computer Engineering & Applied Mathematics, Changsha University, Changsha 410001, ChinaCollege of Computer Engineering & Applied Mathematics, Changsha University, Changsha 410001, ChinaInstitute of Fundamental and Frontier Sciences, University of Electronic Science and Technology of China, Chengdu 610000, ChinaCollege of Computer Engineering & Applied Mathematics, Changsha University, Changsha 410001, ChinaAccumulating evidence progressively indicated that microRNAs (miRNAs) play a significant role in the pathogenesis of diseases through many experimental studies; therefore, developing powerful computational models to identify potential human miRNA–disease associations is vital for an understanding of the disease etiology and pathogenesis. In this paper, a weighted interactive network was firstly constructed by combining known miRNA–disease associations, as well as the integrated similarity between diseases and the integrated similarity between miRNAs. Then, a new computational method implementing the newly weighted interactive network was developed for discovering potential miRNA–disease associations (WINMDA) by integrating the T most similar neighbors and the shortest path algorithm. Simulation results show that WINMDA can achieve reliable area under the receiver operating characteristics (ROC) curve (AUC) results of 0.9183 ± 0.0007 in 5-fold cross-validation, 0.9200 ± 0.0004 in 10-fold cross-validation, 0.9243 in global leave-one-out cross-validation (LOOCV), and 0.8856 in local LOOCV. Furthermore, case studies of colon neoplasms, gastric neoplasms, and prostate neoplasms based on the Human microRNA Disease Database (HMDD) database were implemented, for which 94% (colon neoplasms), 96% (gastric neoplasms), and 96% (prostate neoplasms) of the top 50 predicting miRNAs were confirmed by recent experimental reports, which also demonstrates that WINMDA can effectively uncover potential miRNA–disease associations.http://www.mdpi.com/1422-0067/20/1/110microRNAdiseasesassociation predictioncomputational prediction modelpath selection
collection DOAJ
language English
format Article
sources DOAJ
author Haochen Zhao
Linai Kuang
Xiang Feng
Quan Zou
Lei Wang
spellingShingle Haochen Zhao
Linai Kuang
Xiang Feng
Quan Zou
Lei Wang
A Novel Approach Based on a Weighted Interactive Network to Predict Associations of MiRNAs and Diseases
International Journal of Molecular Sciences
microRNA
diseases
association prediction
computational prediction model
path selection
author_facet Haochen Zhao
Linai Kuang
Xiang Feng
Quan Zou
Lei Wang
author_sort Haochen Zhao
title A Novel Approach Based on a Weighted Interactive Network to Predict Associations of MiRNAs and Diseases
title_short A Novel Approach Based on a Weighted Interactive Network to Predict Associations of MiRNAs and Diseases
title_full A Novel Approach Based on a Weighted Interactive Network to Predict Associations of MiRNAs and Diseases
title_fullStr A Novel Approach Based on a Weighted Interactive Network to Predict Associations of MiRNAs and Diseases
title_full_unstemmed A Novel Approach Based on a Weighted Interactive Network to Predict Associations of MiRNAs and Diseases
title_sort novel approach based on a weighted interactive network to predict associations of mirnas and diseases
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1422-0067
publishDate 2018-12-01
description Accumulating evidence progressively indicated that microRNAs (miRNAs) play a significant role in the pathogenesis of diseases through many experimental studies; therefore, developing powerful computational models to identify potential human miRNA–disease associations is vital for an understanding of the disease etiology and pathogenesis. In this paper, a weighted interactive network was firstly constructed by combining known miRNA–disease associations, as well as the integrated similarity between diseases and the integrated similarity between miRNAs. Then, a new computational method implementing the newly weighted interactive network was developed for discovering potential miRNA–disease associations (WINMDA) by integrating the T most similar neighbors and the shortest path algorithm. Simulation results show that WINMDA can achieve reliable area under the receiver operating characteristics (ROC) curve (AUC) results of 0.9183 ± 0.0007 in 5-fold cross-validation, 0.9200 ± 0.0004 in 10-fold cross-validation, 0.9243 in global leave-one-out cross-validation (LOOCV), and 0.8856 in local LOOCV. Furthermore, case studies of colon neoplasms, gastric neoplasms, and prostate neoplasms based on the Human microRNA Disease Database (HMDD) database were implemented, for which 94% (colon neoplasms), 96% (gastric neoplasms), and 96% (prostate neoplasms) of the top 50 predicting miRNAs were confirmed by recent experimental reports, which also demonstrates that WINMDA can effectively uncover potential miRNA–disease associations.
topic microRNA
diseases
association prediction
computational prediction model
path selection
url http://www.mdpi.com/1422-0067/20/1/110
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