Identification of SARS-CoV-2-induced pathways reveals drug repurposing strategies

• Published in: Science advances Vol. 7; no. 27
• Main Authors: Han, Namshik, Hwang, Woochang, Tzelepis, Konstantinos, Schmerer, Patrick, Yankova, Eliza, MacMahon, Méabh, Lei, Winnie, M Katritsis, Nicholas, Liu, Anika, Felgenhauer, Ulrike, Schuldt, Alison, Harris, Rebecca, Chapman, Kathryn, McCaughan, Frank, Weber, Friedemann, Kouzarides, Tony
• Format: Journal Article
• Language: English
• Published: United States American Association for the Advancement of Science 01-06-2021
• Subjects: Antiviral Agents - metabolism; Antiviral Agents - pharmacology; Antiviral Agents - therapeutic use; Computer Science; Coronavirus; COVID-19 - pathology; COVID-19 - virology; COVID-19 Drug Treatment; Drug Repositioning; Humans; Life Sciences; Neural Networks, Computer; Proguanil - pharmacology; Proguanil - therapeutic use; SARS-CoV-2 - immunology; SARS-CoV-2 - isolation & purification; SARS-CoV-2 - physiology; SciAdv r-articles; Sulfasalazine - pharmacology; Virus Replication - drug effects
• ISSN: 2375-2548; 2375-2548
• DOI: 10.1126/sciadv.abh3032

The global outbreak of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) necessitates the rapid development of new therapies against coronavirus disease 2019 (COVID-19) infection. Here, we present the identification of 200 approved drugs, appropriate for repurposing against COVID-19. We constructed a SARS-CoV-2-induced protein network, based on disease signatures defined by COVID-19 multiomics datasets, and cross-examined these pathways against approved drugs. This analysis identified 200 drugs predicted to target SARS-CoV-2-induced pathways, 40 of which are already in COVID-19 clinical trials, testifying to the validity of the approach. Using artificial neural network analysis, we classified these 200 drugs into nine distinct pathways, within two overarching mechanisms of action (MoAs): viral replication (126) and immune response (74). Two drugs (proguanil and sulfasalazine) implicated in viral replication were shown to inhibit replication in cell assays. This unbiased and validated analysis opens new avenues for the rapid repurposing of approved drugs into clinical trials.