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

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 c...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8245040/
https://www.ncbi.nlm.nih.gov/pubmed/34193418
http://dx.doi.org/10.1126/sciadv.abh3032
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author 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
author_facet 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
author_sort Han, Namshik
collection PubMed
description 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.
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spelling pubmed-82450402021-07-13 Identification of SARS-CoV-2–induced pathways reveals drug repurposing strategies 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 Sci Adv Research Articles 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. American Association for the Advancement of Science 2021-06-30 /pmc/articles/PMC8245040/ /pubmed/34193418 http://dx.doi.org/10.1126/sciadv.abh3032 Text en Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
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
Identification of SARS-CoV-2–induced pathways reveals drug repurposing strategies
title Identification of SARS-CoV-2–induced pathways reveals drug repurposing strategies
title_full Identification of SARS-CoV-2–induced pathways reveals drug repurposing strategies
title_fullStr Identification of SARS-CoV-2–induced pathways reveals drug repurposing strategies
title_full_unstemmed Identification of SARS-CoV-2–induced pathways reveals drug repurposing strategies
title_short Identification of SARS-CoV-2–induced pathways reveals drug repurposing strategies
title_sort identification of sars-cov-2–induced pathways reveals drug repurposing strategies
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8245040/
https://www.ncbi.nlm.nih.gov/pubmed/34193418
http://dx.doi.org/10.1126/sciadv.abh3032
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