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Repurposing clinically available drugs and therapies for pathogenic targets to combat SARS‐CoV‐2

The coronavirus disease 2019 (COVID‐19) pandemic has affected a large portion of the global population, both physically and mentally. Current evidence suggests that the rapidly evolving coronavirus subvariants risk rendering vaccines and antibodies ineffective due to their potential to evade existin...

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Autores principales: Xue, Yiying, Mei, Husheng, Chen, Yisa, Griffin, James D., Liu, Qingsong, Weisberg, Ellen, Yang, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10183156/
https://www.ncbi.nlm.nih.gov/pubmed/37193304
http://dx.doi.org/10.1002/mco2.254
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author Xue, Yiying
Mei, Husheng
Chen, Yisa
Griffin, James D.
Liu, Qingsong
Weisberg, Ellen
Yang, Jing
author_facet Xue, Yiying
Mei, Husheng
Chen, Yisa
Griffin, James D.
Liu, Qingsong
Weisberg, Ellen
Yang, Jing
author_sort Xue, Yiying
collection PubMed
description The coronavirus disease 2019 (COVID‐19) pandemic has affected a large portion of the global population, both physically and mentally. Current evidence suggests that the rapidly evolving coronavirus subvariants risk rendering vaccines and antibodies ineffective due to their potential to evade existing immunity, with enhanced transmission activity and higher reinfection rates that could lead to new outbreaks across the globe. The goal of viral management is to disrupt the viral life cycle as well as to relieve severe symptoms such as lung damage, cytokine storm, and organ failure. In the fight against viruses, the combination of viral genome sequencing, elucidation of the structure of viral proteins, and identifying proteins that are highly conserved across multiple coronaviruses has revealed many potential molecular targets. In addition, the time‐ and cost‐effective repurposing of preexisting antiviral drugs or approved/clinical drugs for these targets offers considerable clinical advantages for COVID‐19 patients. This review provides a comprehensive overview of various identified pathogenic targets and pathways as well as corresponding repurposed approved/clinical drugs and their potential against COVID‐19. These findings provide new insight into the discovery of novel therapeutic strategies that could be applied to the control of disease symptoms emanating from evolving SARS‐CoV‐2 variants.
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spelling pubmed-101831562023-05-15 Repurposing clinically available drugs and therapies for pathogenic targets to combat SARS‐CoV‐2 Xue, Yiying Mei, Husheng Chen, Yisa Griffin, James D. Liu, Qingsong Weisberg, Ellen Yang, Jing MedComm (2020) Reviews The coronavirus disease 2019 (COVID‐19) pandemic has affected a large portion of the global population, both physically and mentally. Current evidence suggests that the rapidly evolving coronavirus subvariants risk rendering vaccines and antibodies ineffective due to their potential to evade existing immunity, with enhanced transmission activity and higher reinfection rates that could lead to new outbreaks across the globe. The goal of viral management is to disrupt the viral life cycle as well as to relieve severe symptoms such as lung damage, cytokine storm, and organ failure. In the fight against viruses, the combination of viral genome sequencing, elucidation of the structure of viral proteins, and identifying proteins that are highly conserved across multiple coronaviruses has revealed many potential molecular targets. In addition, the time‐ and cost‐effective repurposing of preexisting antiviral drugs or approved/clinical drugs for these targets offers considerable clinical advantages for COVID‐19 patients. This review provides a comprehensive overview of various identified pathogenic targets and pathways as well as corresponding repurposed approved/clinical drugs and their potential against COVID‐19. These findings provide new insight into the discovery of novel therapeutic strategies that could be applied to the control of disease symptoms emanating from evolving SARS‐CoV‐2 variants. John Wiley and Sons Inc. 2023-05-14 /pmc/articles/PMC10183156/ /pubmed/37193304 http://dx.doi.org/10.1002/mco2.254 Text en © 2023 The Authors. MedComm published by Sichuan International Medical Exchange & Promotion Association (SCIMEA) and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reviews
Xue, Yiying
Mei, Husheng
Chen, Yisa
Griffin, James D.
Liu, Qingsong
Weisberg, Ellen
Yang, Jing
Repurposing clinically available drugs and therapies for pathogenic targets to combat SARS‐CoV‐2
title Repurposing clinically available drugs and therapies for pathogenic targets to combat SARS‐CoV‐2
title_full Repurposing clinically available drugs and therapies for pathogenic targets to combat SARS‐CoV‐2
title_fullStr Repurposing clinically available drugs and therapies for pathogenic targets to combat SARS‐CoV‐2
title_full_unstemmed Repurposing clinically available drugs and therapies for pathogenic targets to combat SARS‐CoV‐2
title_short Repurposing clinically available drugs and therapies for pathogenic targets to combat SARS‐CoV‐2
title_sort repurposing clinically available drugs and therapies for pathogenic targets to combat sars‐cov‐2
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10183156/
https://www.ncbi.nlm.nih.gov/pubmed/37193304
http://dx.doi.org/10.1002/mco2.254
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