ACE-2, TMPRSS2 and Beyond; Promising Targets and Tools for COVID-19 Prophylaxis and Treatment

Several repurposing drugs and ongoing vaccine researches to combat Coronavirus Disease-19 (COVID-19) are testing clinically, worldwide. COVID-19 caused by severe acute respiratory failure syndrome-CoV-2, uses angiotensin-converting enzyme 2 (ACE-2) as a functional receptor for entry into the cells,...

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Main Authors: Akçahan GEPDİREMEN, Meltem KUMAŞ
Format: Article
Language:English
Published: Galenos Publishing House 2020-12-01
Series:Bezmiâlem Science
Subjects:
Online Access: http://bezmialemscience.org/archives/archive-detail/article-preview/ace-2-tmprss2-and-beyond-promising-targets-and-too/42777
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author Akçahan GEPDİREMEN
Meltem KUMAŞ
author_facet Akçahan GEPDİREMEN
Meltem KUMAŞ
author_sort Akçahan GEPDİREMEN
collection DOAJ
description Several repurposing drugs and ongoing vaccine researches to combat Coronavirus Disease-19 (COVID-19) are testing clinically, worldwide. COVID-19 caused by severe acute respiratory failure syndrome-CoV-2, uses angiotensin-converting enzyme 2 (ACE-2) as a functional receptor for entry into the cells, followed by its priming by transmembrane protease serine 2 (TMPRSS2). Most of the ACE-2 expressing cells are alveolar type II pneumocytes. Viral S-glycoprotein, TMPRSS2 and ACE-2 inhibition, as extracellular media components, are potential targets of future therapy. ACE-2 and/or TMPRSS2 blockade is thought to be beneficial in the prevention or treating of this infection which will be the most convenient for pharmacoeconomics and effectiveness, regarding similar future pandemics. Despite substrate-based design and synthesis of ACE-2 inhibitor compounds were presented almost two decades ago, data on renin angiotensin system activation or its blockers, especially ACE-2, are limited by now. Priority must be given to design a convenient vaccine soon, but due to the high mutation ability of such viruses mean that new vaccines may need to be developed for each outbreak. So, de novo drugs such as ACE-2 or TMPRSS2 blockers need to be developed which can specifically block spike binding sites of the target cells and prevent virus intrusion, especially at the extracellular media, for future pandemics.
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spelling doaj.art-88d08237c4e04c88b81fe272e4ef986c2023-02-15T16:21:07ZengGalenos Publishing HouseBezmiâlem Science2148-23732148-23732020-12-0183798310.14235/bas.galenos.2020.475613049054ACE-2, TMPRSS2 and Beyond; Promising Targets and Tools for COVID-19 Prophylaxis and TreatmentAkçahan GEPDİREMEN0Meltem KUMAŞ1 Bezmialem Vakıf University Medical Faculty, Department of Medical Pharmacology, İstanbul, Turkey Dokuz Eylül University Faculty of Veterinary Medicine, Department of Histology and Embryology, İzmir, Turkey Several repurposing drugs and ongoing vaccine researches to combat Coronavirus Disease-19 (COVID-19) are testing clinically, worldwide. COVID-19 caused by severe acute respiratory failure syndrome-CoV-2, uses angiotensin-converting enzyme 2 (ACE-2) as a functional receptor for entry into the cells, followed by its priming by transmembrane protease serine 2 (TMPRSS2). Most of the ACE-2 expressing cells are alveolar type II pneumocytes. Viral S-glycoprotein, TMPRSS2 and ACE-2 inhibition, as extracellular media components, are potential targets of future therapy. ACE-2 and/or TMPRSS2 blockade is thought to be beneficial in the prevention or treating of this infection which will be the most convenient for pharmacoeconomics and effectiveness, regarding similar future pandemics. Despite substrate-based design and synthesis of ACE-2 inhibitor compounds were presented almost two decades ago, data on renin angiotensin system activation or its blockers, especially ACE-2, are limited by now. Priority must be given to design a convenient vaccine soon, but due to the high mutation ability of such viruses mean that new vaccines may need to be developed for each outbreak. So, de novo drugs such as ACE-2 or TMPRSS2 blockers need to be developed which can specifically block spike binding sites of the target cells and prevent virus intrusion, especially at the extracellular media, for future pandemics. http://bezmialemscience.org/archives/archive-detail/article-preview/ace-2-tmprss2-and-beyond-promising-targets-and-too/42777 ace-2covid-19sars-cov-2raastmprss2coronavirus
spellingShingle Akçahan GEPDİREMEN
Meltem KUMAŞ
ACE-2, TMPRSS2 and Beyond; Promising Targets and Tools for COVID-19 Prophylaxis and Treatment
Bezmiâlem Science
ace-2
covid-19
sars-cov-2
raas
tmprss2
coronavirus
title ACE-2, TMPRSS2 and Beyond; Promising Targets and Tools for COVID-19 Prophylaxis and Treatment
title_full ACE-2, TMPRSS2 and Beyond; Promising Targets and Tools for COVID-19 Prophylaxis and Treatment
title_fullStr ACE-2, TMPRSS2 and Beyond; Promising Targets and Tools for COVID-19 Prophylaxis and Treatment
title_full_unstemmed ACE-2, TMPRSS2 and Beyond; Promising Targets and Tools for COVID-19 Prophylaxis and Treatment
title_short ACE-2, TMPRSS2 and Beyond; Promising Targets and Tools for COVID-19 Prophylaxis and Treatment
title_sort ace 2 tmprss2 and beyond promising targets and tools for covid 19 prophylaxis and treatment
topic ace-2
covid-19
sars-cov-2
raas
tmprss2
coronavirus
url http://bezmialemscience.org/archives/archive-detail/article-preview/ace-2-tmprss2-and-beyond-promising-targets-and-too/42777
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