NDAMDA: Network distance analysis for MiRNA-disease association prediction

被引:29
|
作者
Chen, Xing [1 ]
Wang, Le-Yi [2 ]
Huang, Li [3 ]
机构
[1] China Univ Min & Technol, Sch Informat & Control Engn, Xuzhou, Peoples R China
[2] Wuhan Univ, Sch Math & Stat, Luojiashan, Wuchang, Peoples R China
[3] Natl Univ Singapore, Business Analyt Ctr, Singapore, Singapore
基金
中国国家自然科学基金;
关键词
adjusted network distance; association prediction; disease; microRNA; network integration; GLOBAL CANCER STATISTICS; HUMAN MICRORNA; EXPRESSION; IDENTIFICATION; DEREGULATION; BIOMARKER; GENOMICS; DATABASE; STRESS;
D O I
10.1111/jcmm.13583
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In recent years, microRNAs (miRNAs) are attracting an increasing amount of researchers' attention, as accumulating studies show that miRNAs play important roles in various basic biological processes and that dysregulation of miRNAs is connected with diverse human diseases, particularly cancers. However, the experimental methods to identify associations between miRNAs and diseases remain costly and laborious. In this study, we developed a computational method named Network Distance Analysis for MiRNA-Disease Association prediction (NDAMDA) which could effectively predict potential miRNA-disease associations. The highlight of this method was the use of not only the direct network distance between 2 miRNAs (diseases) but also their respective mean network distances to all other miRNAs (diseases) in the network. The model's reliable performance was certified by the AUC of 0.8920 in global leave-one-out cross-validation (LOOCV), 0.8062 in local LOOCV and the average AUCs of 0.8935 +/- 0.0009 in fivefold cross-validation. Moreover, we applied NDAMDA to 3 different case studies to predict potential miRNAs related to breast neoplasms, lymphoma, oesophageal neoplasms, prostate neoplasms and hepatocellular carcinoma. Results showed that 86%, 72%, 86%, 86% and 84% of the top 50 predicted miRNAs were supported by experimental association evidence. Therefore, NDAMDA is a reliable method for predicting disease-related miRNAs.
引用
收藏
页码:2884 / 2895
页数:12
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