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Exportin 1 inhibition as antiviral therapy
Coronavirus 2019 (COVID-19; caused by Severe Acute Respiratory Syndrome Coronavirus 2; SARS-CoV-2) is a currently global health problem. Previous studies showed that blocking nucleocytoplasmic transport with exportin 1 (XPO1) inhibitors originally developed as anticancer drugs can quarantine key vir...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Ltd.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7305737/ https://www.ncbi.nlm.nih.gov/pubmed/32569833 http://dx.doi.org/10.1016/j.drudis.2020.06.014 |
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author | Uddin, Md. Hafiz Zonder, Jeffrey A. Azmi, Asfar S. |
author_facet | Uddin, Md. Hafiz Zonder, Jeffrey A. Azmi, Asfar S. |
author_sort | Uddin, Md. Hafiz |
collection | PubMed |
description | Coronavirus 2019 (COVID-19; caused by Severe Acute Respiratory Syndrome Coronavirus 2; SARS-CoV-2) is a currently global health problem. Previous studies showed that blocking nucleocytoplasmic transport with exportin 1 (XPO1) inhibitors originally developed as anticancer drugs can quarantine key viral accessory proteins and genomic materials in the nucleus of host cell and reduce virus replication and immunopathogenicity. These observations support the concept of the inhibition of nuclear export as an effective strategy against an array of viruses, including influenza A, B, and SARS-CoV. Clinical studies using the XPO1 inhibitor selinexor as a therapy for COVID-19 infection are in progress. |
format | Online Article Text |
id | pubmed-7305737 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73057372020-06-22 Exportin 1 inhibition as antiviral therapy Uddin, Md. Hafiz Zonder, Jeffrey A. Azmi, Asfar S. Drug Discov Today Feature Coronavirus 2019 (COVID-19; caused by Severe Acute Respiratory Syndrome Coronavirus 2; SARS-CoV-2) is a currently global health problem. Previous studies showed that blocking nucleocytoplasmic transport with exportin 1 (XPO1) inhibitors originally developed as anticancer drugs can quarantine key viral accessory proteins and genomic materials in the nucleus of host cell and reduce virus replication and immunopathogenicity. These observations support the concept of the inhibition of nuclear export as an effective strategy against an array of viruses, including influenza A, B, and SARS-CoV. Clinical studies using the XPO1 inhibitor selinexor as a therapy for COVID-19 infection are in progress. Elsevier Ltd. 2020-10 2020-06-20 /pmc/articles/PMC7305737/ /pubmed/32569833 http://dx.doi.org/10.1016/j.drudis.2020.06.014 Text en © 2020 Elsevier Ltd. 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 | Feature Uddin, Md. Hafiz Zonder, Jeffrey A. Azmi, Asfar S. Exportin 1 inhibition as antiviral therapy |
title | Exportin 1 inhibition as antiviral therapy |
title_full | Exportin 1 inhibition as antiviral therapy |
title_fullStr | Exportin 1 inhibition as antiviral therapy |
title_full_unstemmed | Exportin 1 inhibition as antiviral therapy |
title_short | Exportin 1 inhibition as antiviral therapy |
title_sort | exportin 1 inhibition as antiviral therapy |
topic | Feature |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7305737/ https://www.ncbi.nlm.nih.gov/pubmed/32569833 http://dx.doi.org/10.1016/j.drudis.2020.06.014 |
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