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Crippling life support for SARS-CoV-2 and other viruses through synthetic lethality
With the rapid global spread of SARS-CoV-2, we have become acutely aware of the inadequacies of our ability to respond to viral epidemics. Although disrupting the viral life cycle is critical for limiting viral spread and disease, it has proven challenging to develop targeted and selective therapeut...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7659715/ https://www.ncbi.nlm.nih.gov/pubmed/32785687 http://dx.doi.org/10.1083/jcb.202006159 |
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author | Mast, Fred D. Navare, Arti T. van der Sloot, Almer M. Coulombe-Huntington, Jasmin Rout, Michael P. Baliga, Nitin S. Kaushansky, Alexis Chait, Brian T. Aderem, Alan Rice, Charles M. Sali, Andrej Tyers, Mike Aitchison, John D. |
author_facet | Mast, Fred D. Navare, Arti T. van der Sloot, Almer M. Coulombe-Huntington, Jasmin Rout, Michael P. Baliga, Nitin S. Kaushansky, Alexis Chait, Brian T. Aderem, Alan Rice, Charles M. Sali, Andrej Tyers, Mike Aitchison, John D. |
author_sort | Mast, Fred D. |
collection | PubMed |
description | With the rapid global spread of SARS-CoV-2, we have become acutely aware of the inadequacies of our ability to respond to viral epidemics. Although disrupting the viral life cycle is critical for limiting viral spread and disease, it has proven challenging to develop targeted and selective therapeutics. Synthetic lethality offers a promising but largely unexploited strategy against infectious viral disease; as viruses infect cells, they abnormally alter the cell state, unwittingly exposing new vulnerabilities in the infected cell. Therefore, we propose that effective therapies can be developed to selectively target the virally reconfigured host cell networks that accompany altered cellular states to cripple the host cell that has been converted into a virus factory, thus disrupting the viral life cycle. |
format | Online Article Text |
id | pubmed-7659715 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-76597152020-11-20 Crippling life support for SARS-CoV-2 and other viruses through synthetic lethality Mast, Fred D. Navare, Arti T. van der Sloot, Almer M. Coulombe-Huntington, Jasmin Rout, Michael P. Baliga, Nitin S. Kaushansky, Alexis Chait, Brian T. Aderem, Alan Rice, Charles M. Sali, Andrej Tyers, Mike Aitchison, John D. J Cell Biol Perspective With the rapid global spread of SARS-CoV-2, we have become acutely aware of the inadequacies of our ability to respond to viral epidemics. Although disrupting the viral life cycle is critical for limiting viral spread and disease, it has proven challenging to develop targeted and selective therapeutics. Synthetic lethality offers a promising but largely unexploited strategy against infectious viral disease; as viruses infect cells, they abnormally alter the cell state, unwittingly exposing new vulnerabilities in the infected cell. Therefore, we propose that effective therapies can be developed to selectively target the virally reconfigured host cell networks that accompany altered cellular states to cripple the host cell that has been converted into a virus factory, thus disrupting the viral life cycle. Rockefeller University Press 2020-08-12 /pmc/articles/PMC7659715/ /pubmed/32785687 http://dx.doi.org/10.1083/jcb.202006159 Text en © 2020 Mast et al. https://creativecommons.org/licenses/by-nc-sa/4.0/http://www.rupress.org/terms/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Perspective Mast, Fred D. Navare, Arti T. van der Sloot, Almer M. Coulombe-Huntington, Jasmin Rout, Michael P. Baliga, Nitin S. Kaushansky, Alexis Chait, Brian T. Aderem, Alan Rice, Charles M. Sali, Andrej Tyers, Mike Aitchison, John D. Crippling life support for SARS-CoV-2 and other viruses through synthetic lethality |
title | Crippling life support for SARS-CoV-2 and other viruses through synthetic lethality |
title_full | Crippling life support for SARS-CoV-2 and other viruses through synthetic lethality |
title_fullStr | Crippling life support for SARS-CoV-2 and other viruses through synthetic lethality |
title_full_unstemmed | Crippling life support for SARS-CoV-2 and other viruses through synthetic lethality |
title_short | Crippling life support for SARS-CoV-2 and other viruses through synthetic lethality |
title_sort | crippling life support for sars-cov-2 and other viruses through synthetic lethality |
topic | Perspective |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7659715/ https://www.ncbi.nlm.nih.gov/pubmed/32785687 http://dx.doi.org/10.1083/jcb.202006159 |
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