In Silico Prediction of Potential Drug Combinations for Type 2 Diabetes Mellitus by an Integrated Network and Transcriptome Analysis.
Dan TengYuning GongZengrui WuWeihua LiYun TangGuixia LiuPublished in: ChemMedChem (2021)
Type 2 diabetes mellitus (T2DM) is a heterogeneous disorder, so achieving the desired therapeutic efficacy through monotherapy is tricky. Drug combinations play a vital role in treating multiple complex diseases by providing increased efficacy and reduced toxicity. Here, we adopted a computational framework to discover potential drugs and drug pairs for T2DM. Firstly, we collected T2DM-associated genes and constructed the disease module for T2DM. Then, by quantifying the proximity between drugs and the disease module, we found out potential drugs. Based on the drug-induced gene expression profiles, we further performed Gene Set Enrichment Analysis (GSEA) on these drugs and identified several potential candidates. In addition, through network-based separation, potential drug combinations for T2DM were predicted. Results from this study could provide insights for anti-T2DM drug discovery and rational drug use of existing agents. As a useful computational framework, our approach could also be applied in drug research for other complex diseases.
Keyphrases
- drug induced
- liver injury
- glycemic control
- adverse drug
- drug discovery
- human health
- genome wide
- type diabetes
- risk assessment
- oxidative stress
- clinical trial
- randomized controlled trial
- copy number
- mass spectrometry
- emergency department
- molecular docking
- study protocol
- combination therapy
- open label
- liquid chromatography