Multiple-Molecule Drug Repositioning for Disrupting Progression of SARS-CoV-2 Infection by Utilizing the Systems Biology Method through Host-Pathogen-Interactive Time Profile Data and DNN-Based DTI Model with Drug Design Specifications

• الحاوية / القاعدة: Stresses
• المؤلفون الرئيسيون: Cheng-Gang Wang, Bor-Sen Chen
• التنسيق: مقال
• اللغة: الإنجليزية
• منشور في: MDPI AG 2022-11-01
• الموضوعات: SARS-CoV-2; COVID-19; systems biology; reverse engineering; principal network projection (PNP); drug–target interaction (DTI) model
• الوصول للمادة أونلاين: https://www.mdpi.com/2673-7140/2/4/29

The coronavirus disease 2019 (COVID-19) pandemic has claimed many lives since it was first reported in late December 2019. However, there is still no drug proven to be effective against the virus. In this study, a candidate host–pathogen–interactive (HPI) genome-wide genetic and epigenetic network (HPI-GWGEN) was constructed via big data mining. The reverse engineering method was applied to investigate the pathogenesis of SARS-CoV-2 infection by pruning the false positives in candidate HPI-GWGEN through the HPI RNA-seq time profile data. Subsequently, using the principal network projection (PNP) method and the annotations of the Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway, we identified the significant biomarkers usable as drug targets for destroying favorable environments for the replication of SARS-CoV-2 or enhancing the defense of host cells against it. To discover multiple-molecule drugs that target the significant biomarkers (as drug targets), a deep neural network (DNN)-based drug–target interaction (DTI) model was trained by DTI databases to predict candidate molecular drugs for these drug targets. Using the DNN-based DTI model, we predicted the candidate drugs targeting the significant biomarkers (drug targets). After screening candidate drugs with drug design specifications, we finally proposed the combination of bosutinib, erlotinib, and 17-beta-estradiol as a multiple-molecule drug for the treatment of the amplification stage of SARS-CoV-2 infection and the combination of erlotinib, 17-beta-estradiol, and sertraline as a multiple-molecule drug for the treatment of saturation stage of mild-to-moderate SARS-CoV-2 infection.