PI3K/Akt/mTOR pathway: a potential target for anti-SARS-CoV-2 therapy
Coronavirus disease 2019 (COVID-19) is a viral infection caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). A single-stranded RNA virus from a β-Coronaviridae family causes acute clinical manifestations. Its high death rate and severe clinical symptoms have turned it into the mo...
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Published in | Immunologic research Vol. 70; no. 3; pp. 269 - 275 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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Springer US
01.06.2022
Springer Nature B.V |
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Abstract | Coronavirus disease 2019 (COVID-19) is a viral infection caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). A single-stranded RNA virus from a β-Coronaviridae family causes acute clinical manifestations. Its high death rate and severe clinical symptoms have turned it into the most significant challenge worldwide. Up until now, several effective COVID-19 vaccines have been designed and marketed, but our data on specialized therapeutic drugs for the treatment of COVID-19 is still limited. In order to synthesis virus particles, SARS-CoV-2 uses host metabolic pathways such as phosphoinositide3-kinase (PI3K)/protein kinase B (PKB, also known as AKT)/mammalian target of rapamycin (mTOR). mTOR is involved in multiple biological processes. Over-activation of the mTOR pathway improves viral replication, which makes it a possible target in COVID-19 therapy. Clinical data shows the hyperactivation of the mTOR pathway in lung tissues during respiratory viral infections. However, the exact impact of mTOR pathway inhibitors on the COVID-19 severity and death rate is yet to be thoroughly investigated. There are several mTOR pathway inhibitors. Rapamycin is the most famous inhibitor of mTORC1 among all. Studies on other respiratory viruses suggest that the therapeutic inhibitors of the mTOR pathway, especially rapamycin, can be a potential approach to anti-SARS-CoV-2 therapy. Using therapeutic methods that inhibit harmful immune responses can open a new chapter in treating severe COVID-19 disease. We highlighted the potential contribution of PI3K/Akt/mTOR inhibitors in the treatment of COVID-19. |
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AbstractList | Coronavirus disease 2019 (COVID-19) is a viral infection caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). A single-stranded RNA virus from a β-Coronaviridae family causes acute clinical manifestations. Its high death rate and severe clinical symptoms have turned it into the most significant challenge worldwide. Up until now, several effective COVID-19 vaccines have been designed and marketed, but our data on specialized therapeutic drugs for the treatment of COVID-19 is still limited. In order to synthesis virus particles, SARS-CoV-2 uses host metabolic pathways such as phosphoinositide3-kinase (PI3K)/protein kinase B (PKB, also known as AKT)/mammalian target of rapamycin (mTOR). mTOR is involved in multiple biological processes. Over-activation of the mTOR pathway improves viral replication, which makes it a possible target in COVID-19 therapy. Clinical data shows the hyperactivation of the mTOR pathway in lung tissues during respiratory viral infections. However, the exact impact of mTOR pathway inhibitors on the COVID-19 severity and death rate is yet to be thoroughly investigated. There are several mTOR pathway inhibitors. Rapamycin is the most famous inhibitor of mTORC1 among all. Studies on other respiratory viruses suggest that the therapeutic inhibitors of the mTOR pathway, especially rapamycin, can be a potential approach to anti-SARS-CoV-2 therapy. Using therapeutic methods that inhibit harmful immune responses can open a new chapter in treating severe COVID-19 disease. We highlighted the potential contribution of PI3K/Akt/mTOR inhibitors in the treatment of COVID-19. |
Author | Mafi, Sahar Mohammad-Rezaei, Mina Khalifehzadeh-Esfahani, Zahra Fattahi, Soheila Jafarinia, Morteza |
Author_xml | – sequence: 1 givenname: Soheila surname: Fattahi fullname: Fattahi, Soheila organization: Cellular and Molecular Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences – sequence: 2 givenname: Zahra surname: Khalifehzadeh-Esfahani fullname: Khalifehzadeh-Esfahani, Zahra organization: Immunology Department, Faculty of Medicine, Isfahan University of Medical Sciences – sequence: 3 givenname: Mina surname: Mohammad-Rezaei fullname: Mohammad-Rezaei, Mina organization: Immunology Research Center, Iran University of Medical Sciences, Department of Immunology, School of Medicine, Iran University of Medical Sciences – sequence: 4 givenname: Sahar surname: Mafi fullname: Mafi, Sahar organization: Medical Plants Research Center, Yasuj University of Medical Sciences, Department of Clinical Biochemistry, Yasuj University of Medical Sciences – sequence: 5 givenname: Morteza orcidid: 0000-0002-3272-448X surname: Jafarinia fullname: Jafarinia, Morteza email: morteza_jaafarinia@yahoo.com organization: Shiraz Neuroscience Research Center, Shiraz University of Medical Sciences |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/35107743$$D View this record in MEDLINE/PubMed |
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Keywords | COVID-19 mTOR inhibitors Rapamycin; SARS-CoV-2 PI3K/Akt/ mTOR pathway |
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License | 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
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