GCAEMDA: Predicting miRNA-disease associations via graph convolutional autoencoder

PLoS Comput Biol. 2021 Dec 10;17(12):e1009655. doi: 10.1371/journal.pcbi.1009655. eCollection 2021 Dec.

Abstract

microRNAs (miRNAs) are small non-coding RNAs related to a number of complicated biological processes. A growing body of studies have suggested that miRNAs are closely associated with many human diseases. It is meaningful to consider disease-related miRNAs as potential biomarkers, which could greatly contribute to understanding the mechanisms of complex diseases and benefit the prevention, detection, diagnosis and treatment of extraordinary diseases. In this study, we presented a novel model named Graph Convolutional Autoencoder for miRNA-Disease Association Prediction (GCAEMDA). In the proposed model, we utilized miRNA-miRNA similarities, disease-disease similarities and verified miRNA-disease associations to construct a heterogeneous network, which is applied to learn the embeddings of miRNAs and diseases. In addition, we separately constructed miRNA-based and disease-based sub-networks. Combining the embeddings of miRNAs and diseases, graph convolutional autoencoder (GCAE) was utilized to calculate association scores of miRNA-disease on two sub-networks, respectively. Furthermore, we obtained final prediction scores between miRNAs and diseases by adopting an average ensemble way to integrate the prediction scores from two types of subnetworks. To indicate the accuracy of GCAEMDA, we applied different cross validation methods to evaluate our model whose performances were better than the state-of-the-art models. Case studies on a common human diseases were also implemented to prove the effectiveness of GCAEMDA. The results demonstrated that GCAEMDA was beneficial to infer potential associations of miRNA-disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Algorithms
  • Area Under Curve
  • Computational Biology / methods
  • Genetic Predisposition to Disease / genetics*
  • Humans
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism
  • Models, Genetic*
  • Neoplasms / genetics
  • Neoplasms / metabolism
  • Neural Networks, Computer*

Substances

  • MicroRNAs

Grants and funding

This work was supported by the National Natural Science Foundation of China through grants 61873001 (C.Z., Y.W.), U19A2064 (C.Z.) and 11701318 (Y.W.), the Natural Science Foundation of Shandong Province grant ZR2020KC022 (J.N., Y.W., C.J., L.L) and the Open Project of Anhui Provincial Key Laboratory of Multimodal Cognitive Computation, Anhui University, No. MMC202006 (Y.W., L.L). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.