School of Computer Science, Qufu Normal University, Rizhao 276826, China.
School of Information and Control Engineering, Qingdao University of Technology, Qingdao 266520, China.
Molecules. 2022 Jul 7;27(14):4371. doi: 10.3390/molecules27144371.
Many microRNAs (miRNAs) have been confirmed to be associated with the generation of human diseases. Capturing miRNA-disease associations (M-DAs) provides an effective way to understand the etiology of diseases. Many models for predicting M-DAs have been constructed; nevertheless, there are still several limitations, such as generally considering direct information between miRNAs and diseases, usually ignoring potential knowledge hidden in isolated miRNAs or diseases. To overcome these limitations, in this study a novel method for predicting M-DAs was developed named TLNPMD, highlights of which are the introduction of drug heuristic information and a bipartite network reconstruction strategy. Specifically, three bipartite networks, including drug-miRNA, drug-disease, and miRNA-disease, were reconstructed as weighted ones using such reconstruction strategy. Based on these weighted bipartite networks, as well as three corresponding similarity networks of drugs, miRNAs and diseases, the miRNA-drug-disease three-layer heterogeneous network was constructed. Then, this heterogeneous network was converted into three two-layer heterogeneous networks, for each of which the network path computational model was employed to predict association scores. Finally, both direct and indirect miRNA-disease paths were used to predict M-DAs. Comparative experiments of TLNPMD and other four models were performed and evaluated by five-fold and global leave-one-out cross validations, results of which show that TLNPMD has the highest AUC values among those of compared methods. In addition, case studies of two common diseases were carried out to validate the effectiveness of the TLNPMD. These experiments demonstrate that the TLNPMD may serve as a promising alternative to existing methods for predicting M-DAs.
许多 microRNAs(miRNAs)已被证实与人类疾病的发生有关。捕获 miRNA-疾病关联(M-DAs)提供了一种了解疾病病因的有效方法。已经构建了许多用于预测 M-DAs 的模型;然而,仍然存在一些局限性,例如通常只考虑 miRNA 和疾病之间的直接信息,通常忽略隐藏在孤立的 miRNA 或疾病中的潜在知识。为了克服这些局限性,本研究提出了一种新的 miRNA-疾病关联预测方法,命名为 TLNPMD,其主要特点是引入药物启发式信息和二分网络重建策略。具体来说,使用这种重建策略,将包括药物-miRNA、药物-疾病和 miRNA-疾病在内的三个二分网络重建为加权网络。基于这些加权二分网络,以及药物、miRNA 和疾病的三个相应相似性网络,构建了 miRNA-药物-疾病三层异质网络。然后,将这个异质网络转化为三个两层异质网络,对于每个网络,都采用网络路径计算模型来预测关联分数。最后,使用直接和间接的 miRNA-疾病路径来预测 M-DAs。通过五重和全局留一交叉验证对 TLNPMD 和其他四个模型进行了比较实验,并对其进行了评估,结果表明 TLNPMD 在比较方法中的 AUC 值最高。此外,还对两种常见疾病进行了案例研究,以验证 TLNPMD 的有效性。这些实验表明,TLNPMD 可能成为现有预测 M-DAs 方法的一种有前途的替代方法。