College of Computer Science and Electronic Engineering, Hunan University, Changsha 410083, China.
School of Computer Science, University of South China, Hengyang 421001, China.
J Chem Inf Model. 2020 Dec 28;60(12):6709-6721. doi: 10.1021/acs.jcim.0c00975. Epub 2020 Nov 9.
MicroRNAs (miRNAs) are significant regulators of post-transcriptional levels and have been confirmed to be targeted by small molecule (SM) drugs. It is a novel insight to treat human diseases and accelerate drug discovery by targeting miRNA with small molecules. Computational approaches for discovering novel small molecule-miRNA associations by integrating more heterogeneous network information provide a new idea for the multiple node association prediction between small molecule-miRNA and small molecule-disease associations at a system level. In this study, we proposed a new computational model based on graph regularization techniques in heterogeneous networks, called identification of small molecule-miRNA associations with graph regularization techniques (SMMARTs), to discover potential small molecule-miRNA associations. The novelty of the model lies in the fact that the association score of a small molecule-miRNA pair is calculated by an iterative method in heterogeneous networks that incorporates small molecule-disease associations and miRNA-disease associations. The experimental results indicate that SMMART has better performance than several state-of-the-art methods in inferring small molecule-miRNA associations. Case studies further illustrate the effectiveness of SMMART for small molecule-miRNA association prediction.
微小 RNA(miRNAs)是转录后水平的重要调控因子,已被证实可被小分子(SM)药物靶向。通过小分子靶向 miRNA 来治疗人类疾病和加速药物发现是一种新的见解。通过整合更多异构网络信息来发现新型小分子-miRNA 关联的计算方法为小分子-miRNA 和小分子-疾病关联在系统水平上的多个节点关联预测提供了新的思路。在这项研究中,我们提出了一种基于异构网络中图正则化技术的新计算模型,称为基于图正则化技术识别小分子-miRNA 关联(SMMARTs),以发现潜在的小分子-miRNA 关联。该模型的新颖之处在于,通过在异构网络中采用迭代方法计算小分子-miRNA 对的关联分数,该方法整合了小分子-疾病关联和 miRNA-疾病关联。实验结果表明,SMMART 在推断小分子-miRNA 关联方面的性能优于几种最先进的方法。案例研究进一步说明了 SMMART 对小分子-miRNA 关联预测的有效性。