Abstract

MicroRNAs (miRNAs) are one class of important noncoding RNA molecules, and their dysfunction is associated with a number of diseases. Currently, a series of databases and algorithms have been developed for dissecting human miRNA–disease associations. However, these tools only presented the associations between miRNAs and disease but did not address whether the associations are causal or not, a key biomedical issue that is critical for understanding the roles of candidate miRNAs in the mechanisms of specific diseases. Here we first manually curated causal miRNA–disease association information and updated the human miRNA disease database (HMDD) accordingly. Then we built a computational model, MDCAP (MiRNA-Disease Causal Association Predictor), to predict novel causal miRNA–disease associations. As a result, we collected 6,667 causal miRNA–disease associations between 616 miRNAs and 440 diseases, which accounts for ∼20% of the total data in HMDD. The MDCAP model achieved an area under the receiver operating characteristic (ROC) curve of 0.928 for ROC analysis by independent test and an area under the ROC curve of 0.925 for ROC analysis by 10-fold cross-validation. Finally, case studies conducted on myocardial infarction and hsa-mir-498 further suggested the biomedical significance of the predictions.

Highlights

  • MicroRNAs are a class of ~22-nucleotide-long small noncoding RNA that mediate gene posttranscriptional regulation

  • We assigned all miRNAs in human miRNA disease database (HMDD) v3.1 into five groups according to their causal disease numbers

  • We found that ~50% of all the miRNAs have no causal information for any diseases, while ~3% of all the miRNAs are causal in more than 30 diseases (Figure 3B)

Read more

Summary

Introduction

MicroRNAs (miRNAs) are a class of ~22-nucleotide-long small noncoding RNA that mediate gene posttranscriptional regulation. The dysfunction of miRNAs is associated with large number of diseases, including but not limited to cancers, cardiovascular diseases (CVDs), and neurological disorders (Esteller, 2011; Small and Olson, 2011; Wang et al, 2019b). Databases for miRNA–disease associations are increasingly important for dissecting the roles of miRNAs in diseases. For this purpose, in 2007, we built the human miRNA disease database (HMDD) (Lu et al, 2008) and launched versions 2 and 3 in 2013 and 2018, respectively (Li et al, 2014; Huang et al, 2019).

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call