4.6 Article

MLMD: Metric Learning for Predicting MiRNA-Disease Associations

期刊

IEEE ACCESS
卷 9, 期 -, 页码 78847-78858

出版社

IEEE-INST ELECTRICAL ELECTRONICS ENGINEERS INC
DOI: 10.1109/ACCESS.2021.3084148

关键词

Diseases; Measurement; Computational modeling; Predictive models; Prediction algorithms; Proteins; Biological system modeling; miRNA; disease; metric learning; latent vector; omics data integration; biomarker

资金

  1. Basic Science Research Program through the National Research Foundation of Korea (NRF) by the Ministry of Education [NRF-2019R1I1A1A01058458]
  2. Kangwon National University

向作者/读者索取更多资源

miRNAs play crucial roles in regulating biological functions and disease incidence. Identifying novel disease-related miRNAs can help understand disease etiology. The computational model MLMD is effective in predicting miRNA-disease associations, providing clues for understanding human complex diseases.
The crucial roles played by microRNAs (miRNAs) in regulating various biological functions and in disease incidence have been reported continuously over the past decades. Therefore, the identification of novel disease-related miRNAs could help in understanding human disease etiology and pathogenesis further. Due to the involvement of high cost and more time in clinical experiments, development of accurate and feasible computational models is considered highly significant. Here, we aim to present a novel computational model of metric learning for predicting miRNA-disease associations (MLMD). MLMD aims at learning miRNA-disease metric to unravel not only novel disease-related miRNAs but also the miRNA-miRNA and disease-disease similarities. Comprehensive experimental results clearly proved the outstanding performance of MLMD compared to several state-of-the-art methods. MLMD achieved a reliable AUC score of 0.9106 and 0.8786 in the framework of global and local leave-one-out cross validations (LOOCV), respectively. Furthermore, we implemented case studies on two major human cancers (breast cancer and lung cancer) for comparative analysis with already known disease-related miRNAs. Results revealed the top 50 potential candidates were all disease-related miRNAs based on human public databases and literature analysis. We conclude that MLMD could not only serve as practical and feasible framework for inferring potential miRNA-disease associations, but also provide clues for understanding the human complex diseases.

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