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TLNPMD: Prediction of miRNA-Disease Associations Based on miRNA-Drug-Disease Three-Layer Heterogeneous Network.
Yang, Yi; Shang, Junliang; Sun, Yan; Li, Feng; Zhang, Yuanyuan; Kong, Xiang-Zhen; Li, Shengjun; Liu, Jin-Xing.
Affiliation
  • Yang Y; School of Computer Science, Qufu Normal University, Rizhao 276826, China.
  • Shang J; School of Computer Science, Qufu Normal University, Rizhao 276826, China.
  • Sun Y; School of Computer Science, Qufu Normal University, Rizhao 276826, China.
  • Li F; School of Computer Science, Qufu Normal University, Rizhao 276826, China.
  • Zhang Y; School of Information and Control Engineering, Qingdao University of Technology, Qingdao 266520, China.
  • Kong XZ; School of Computer Science, Qufu Normal University, Rizhao 276826, China.
  • Li S; School of Computer Science, Qufu Normal University, Rizhao 276826, China.
  • Liu JX; School of Computer Science, Qufu Normal University, Rizhao 276826, China.
Molecules ; 27(14)2022 Jul 07.
Article de En | MEDLINE | ID: mdl-35889243
ABSTRACT
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.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: MicroARN Type d'étude: Prognostic_studies / Risk_factors_studies Limites: Humans Langue: En Journal: Molecules Sujet du journal: BIOLOGIA Année: 2022 Type de document: Article Pays d'affiliation: Chine

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: MicroARN Type d'étude: Prognostic_studies / Risk_factors_studies Limites: Humans Langue: En Journal: Molecules Sujet du journal: BIOLOGIA Année: 2022 Type de document: Article Pays d'affiliation: Chine
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