Predicting microRNA–disease associations from lncRNA–microRNA interactions via Multiview Multitask Learning

Author:

Huang Yu-An1,Chan Keith C C2,You Zhu-Hong3,Hu Pengwei4,Wang Lei5ORCID,Huang Zhi-An6

Affiliation:

1. Department of Computing at the Hong Kong Polytechnic University

2. Systems Design Engineering from the University of Waterloo, Canada

3. University of Science & Technology of China

4. Department of Computing, The Hong Kong Polytechnic University, Hong Kong

5. China University of Mining and Technology

6. City University of Hong Kong

Abstract

Abstract Motivation Identifying microRNAs that are associated with different diseases as biomarkers is a problem of great medical significance. Existing computational methods for uncovering such microRNA-diseases associations (MDAs) are mostly developed under the assumption that similar microRNAs tend to associate with similar diseases. Since such an assumption is not always valid, these methods may not always be applicable to all kinds of MDAs. Considering that the relationship between long noncoding RNA (lncRNA) and different diseases and the co-regulation relationships between the biological functions of lncRNA and microRNA have been established, we propose here a multiview multitask method to make use of the known lncRNA–microRNA interaction to predict MDAs on a large scale. The investigation is performed in the absence of complete information of microRNAs and any similarity measurement for it and to the best knowledge, the work represents the first ever attempt to discover MDAs based on lncRNA–microRNA interactions. Results In this paper, we propose to develop a deep learning model called MVMTMDA that can create a multiview representation of microRNAs. The model is trained based on an end-to-end multitasking approach to machine learning so that, based on it, missing data in the side information can be determined automatically. Experimental results show that the proposed model yields an average area under ROC curve of 0.8410+/−0.018, 0.8512+/−0.012 and 0.8521+/−0.008 when k is set to 2, 5 and 10, respectively. In addition, we also propose here a statistical approach to predicting lncRNA-disease associations based on these associations and the MDA discovered using MVMTMDA. Availability Python code and the datasets used in our studies are made available at https://github.com/yahuang1991polyu/MVMTMDA/.

Funder

National Natural Science Foundation of China

Publisher

Oxford University Press (OUP)

Subject

Molecular Biology,Information Systems

Reference33 articles.

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2. Genome-wide changes in lncRNA, splicing, and regional gene expression patterns in autism;Parikshak;Nature,2016

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4. HMDD v3. 0: a database for experimentally supported human microRNA–disease associations;Huang;Nuclei Acids Res,2018

5. Identification of cancer-related miRNA–lncRNA biomarkers using a basic miRNA–lncRNA network;Zhang;Plos One,2018

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