Abstract

MicroRNAs (miRNAs) that belong to non-coding RNAs are verified to be closely associated with several complicated biological processes and human diseases. In this study, we proposed a novel model that was Similarity Network Fusion and Inductive Matrix Completion for miRNA-Disease Association Prediction (SNFIMCMDA). We applied inductive matrix completion (IMC) method to acquire possible associations between miRNAs and diseases, which also could obtain corresponding correlation scores. IMC was performed based on the verified connections of miRNA–disease, miRNA similarity, and disease similarity. In addition, miRNA similarity and disease similarity were calculated by similarity network fusion, which could masterly integrate multiple data types to obtain target data. We integrated miRNA functional similarity and Gaussian interaction profile kernel similarity by similarity network fusion to obtain miRNA similarity. Similarly, disease similarity was integrated in this way. To indicate the utility and effectiveness of SNFIMCMDA, we both applied global leave-one-out cross-validation and five-fold cross-validation to validate our model. Furthermore, case studies on three significant human diseases were also implemented to prove the effectiveness of SNFIMCMDA. The results demonstrated that SNFIMCMDA was effective for prediction of possible associations of miRNA–disease.

Highlights

  • MicroRNAs belong to small non-coding RNAs, which effectively control the expression of their mRNA targets through RNA cleavage or translation repression (Ambros, 2004; Bartel, 2004; Ambros, 2001)

  • We constructed the novel model of SNFIMCMDA

  • The prediction score of each miRNA–disease pair was calculated by combining the known association between miRNAs and diseases and integrated similarities of both miRNA and disease in the SNFIMCMDA

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Summary

Introduction

MicroRNAs (miRNAs) belong to small non-coding RNAs, which effectively control the expression of their mRNA targets through RNA cleavage or translation repression (Ambros, 2004; Bartel, 2004; Ambros, 2001). Researchers have discovered various of miRNAs in many living organisms (Bruce et al, 1993; Calin and Croce, 2006). The expression of a great quantity of target genes is controlled by miRNAs, with the result that the whole miRNA pathway is an important technique for gene expression control (Xu et al, 2004; Miska, 2005; Bartel, 2009). The dysregulation of miRNAs results in progression of various diseases and conduces to developmental defects (Meola et al, 2009). During the past few years, traditional experiments have confirmed a large number of connections of miRNA–disease

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