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Endoplasmic reticulum secretory pathway: Potential target against SARS-CoV-2
Coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has recently emerged throughout the world, resulting in more than 400 million cases and over 6 million deaths worldwide as of January 2022. Coronaviruses subvert or use certain aspects of the...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9387115/ https://www.ncbi.nlm.nih.gov/pubmed/35988898 http://dx.doi.org/10.1016/j.virusres.2022.198897 |
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author | Upadhyay, Maarisha Gupta, Sanjeev |
author_facet | Upadhyay, Maarisha Gupta, Sanjeev |
author_sort | Upadhyay, Maarisha |
collection | PubMed |
description | Coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has recently emerged throughout the world, resulting in more than 400 million cases and over 6 million deaths worldwide as of January 2022. Coronaviruses subvert or use certain aspects of the unfolded protein response in the endoplasmic reticulum to overcome protein translation shutdown to benefit their replication. New virions use the ER-Golgi intermediate compartment to assemble and gain transportation to the cell membrane. Extensive remodeling of the ER has been demonstrated during SARS-CoV-2 infection. In this review article, we discuss the role of the endoplasmic reticulum secretory pathway in the replication cycle of SARS-CoV-2. Currently, there is a dearth of therapeutic options for intervening with SARS-CoV-2 infection. To accelerate drug development, efforts around the globe have been focusing on repurposing drugs that have already been approved for clinical use by regulatory agencies. Targeting the ERS pathway is reasonable, as prior work has shown that SARS-CoV-2 egress is dependent on this pathway. Here we discuss the feasibility of off-patent, FDA-approved, pharmacological inhibitors of the ERS pathway to suppress the SARS-CoV-2 replication cycle, a promising approach that warrants investigation. |
format | Online Article Text |
id | pubmed-9387115 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93871152022-08-18 Endoplasmic reticulum secretory pathway: Potential target against SARS-CoV-2 Upadhyay, Maarisha Gupta, Sanjeev Virus Res Article Coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has recently emerged throughout the world, resulting in more than 400 million cases and over 6 million deaths worldwide as of January 2022. Coronaviruses subvert or use certain aspects of the unfolded protein response in the endoplasmic reticulum to overcome protein translation shutdown to benefit their replication. New virions use the ER-Golgi intermediate compartment to assemble and gain transportation to the cell membrane. Extensive remodeling of the ER has been demonstrated during SARS-CoV-2 infection. In this review article, we discuss the role of the endoplasmic reticulum secretory pathway in the replication cycle of SARS-CoV-2. Currently, there is a dearth of therapeutic options for intervening with SARS-CoV-2 infection. To accelerate drug development, efforts around the globe have been focusing on repurposing drugs that have already been approved for clinical use by regulatory agencies. Targeting the ERS pathway is reasonable, as prior work has shown that SARS-CoV-2 egress is dependent on this pathway. Here we discuss the feasibility of off-patent, FDA-approved, pharmacological inhibitors of the ERS pathway to suppress the SARS-CoV-2 replication cycle, a promising approach that warrants investigation. Elsevier B.V. 2022-10-15 2022-08-18 /pmc/articles/PMC9387115/ /pubmed/35988898 http://dx.doi.org/10.1016/j.virusres.2022.198897 Text en © 2022 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Upadhyay, Maarisha Gupta, Sanjeev Endoplasmic reticulum secretory pathway: Potential target against SARS-CoV-2 |
title | Endoplasmic reticulum secretory pathway: Potential target against SARS-CoV-2 |
title_full | Endoplasmic reticulum secretory pathway: Potential target against SARS-CoV-2 |
title_fullStr | Endoplasmic reticulum secretory pathway: Potential target against SARS-CoV-2 |
title_full_unstemmed | Endoplasmic reticulum secretory pathway: Potential target against SARS-CoV-2 |
title_short | Endoplasmic reticulum secretory pathway: Potential target against SARS-CoV-2 |
title_sort | endoplasmic reticulum secretory pathway: potential target against sars-cov-2 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9387115/ https://www.ncbi.nlm.nih.gov/pubmed/35988898 http://dx.doi.org/10.1016/j.virusres.2022.198897 |
work_keys_str_mv | AT upadhyaymaarisha endoplasmicreticulumsecretorypathwaypotentialtargetagainstsarscov2 AT guptasanjeev endoplasmicreticulumsecretorypathwaypotentialtargetagainstsarscov2 |