Systems biology and machine learning approaches identify drug targets in diabetic nephropathy.

Journal: Scientific reports
PMID:

Abstract

Diabetic nephropathy (DN), the leading cause of end-stage renal disease, has become a massive global health burden. Despite considerable efforts, the underlying mechanisms have not yet been comprehensively understood. In this study, a systematic approach was utilized to identify the microRNA signature in DN and to introduce novel drug targets (DTs) in DN. Using microarray profiling followed by qPCR confirmation, 13 and 6 differentially expressed (DE) microRNAs were identified in the kidney cortex and medulla, respectively. The microRNA-target interaction networks for each anatomical compartment were constructed and central nodes were identified. Moreover, enrichment analysis was performed to identify key signaling pathways. To develop a strategy for DT prediction, the human proteome was annotated with 65 biochemical characteristics and 23 network topology parameters. Furthermore, all proteins targeted by at least one FDA-approved drug were identified. Next, mGMDH-AFS, a high-performance machine learning algorithm capable of tolerating massive imbalanced size of the classes, was developed to classify DT and non-DT proteins. The sensitivity, specificity, accuracy, and precision of the proposed method were 90%, 86%, 88%, and 89%, respectively. Moreover, it significantly outperformed the state-of-the-art (P-value ≤ 0.05) and showed very good diagnostic accuracy and high agreement between predicted and observed class labels. The cortex and medulla networks were then analyzed with this validated machine to identify potential DTs. Among the high-rank DT candidates are Egfr, Prkce, clic5, Kit, and Agtr1a which is a current well-known target in DN. In conclusion, a combination of experimental and computational approaches was exploited to provide a holistic insight into the disorder for introducing novel therapeutic targets.

Authors

  • Maryam Abedi
    Regenerative Medicine Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.
  • Hamid Reza Marateb
    Biomedical Engineering DepartmentEngineering FacultyUniversity of Isfahan Isfahan 8415683111 Iran.
  • Mohammad Reza Mohebian
    Department of Electrical and Computer Engineering, University of Saskatchewan, Saskatoon, Canada.
  • Seyed Hamid Aghaee-Bakhtiari
    Bioinformatics Research Group, Mashhad University of Medical Sciences, Mashhad, Iran.
  • Seyed Mahdi Nassiri
    Department of Clinical Pathology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran.
  • Yousof Gheisari
    Regenerative Medicine Research Center, Isfahan University of Medical Sciences, Isfahan, Iran. ygheisari@med.mui.ac.ir.