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DHFR Inhibitors Display a Pleiotropic Anti-Viral Activity against SARS-CoV-2: Insights into the Mechanisms of Action
During the COVID-19 pandemic, drug repurposing represented an effective strategy to obtain quick answers to medical emergencies. Based on previous data on methotrexate (MTX), we evaluated the anti-viral activity of several DHFR inhibitors in two cell lines. We observed that this class of compounds s...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10221469/ https://www.ncbi.nlm.nih.gov/pubmed/37243214 http://dx.doi.org/10.3390/v15051128 |
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author | Iaconis, Daniela Caccuri, Francesca Manelfi, Candida Talarico, Carmine Bugatti, Antonella Filippini, Federica Zani, Alberto Novelli, Rubina Kuzikov, Maria Ellinger, Bernhard Gribbon, Philip Riecken, Kristoffer Esposito, Francesca Corona, Angela Tramontano, Enzo Beccari, Andrea Rosario Caruso, Arnaldo Allegretti, Marcello |
author_facet | Iaconis, Daniela Caccuri, Francesca Manelfi, Candida Talarico, Carmine Bugatti, Antonella Filippini, Federica Zani, Alberto Novelli, Rubina Kuzikov, Maria Ellinger, Bernhard Gribbon, Philip Riecken, Kristoffer Esposito, Francesca Corona, Angela Tramontano, Enzo Beccari, Andrea Rosario Caruso, Arnaldo Allegretti, Marcello |
author_sort | Iaconis, Daniela |
collection | PubMed |
description | During the COVID-19 pandemic, drug repurposing represented an effective strategy to obtain quick answers to medical emergencies. Based on previous data on methotrexate (MTX), we evaluated the anti-viral activity of several DHFR inhibitors in two cell lines. We observed that this class of compounds showed a significant influence on the virus-induced cytopathic effect (CPE) partly attributed to the intrinsic anti-metabolic activity of these drugs, but also to a specific anti-viral function. To elucidate the molecular mechanisms, we took advantage of our EXSCALATE platform for in-silico molecular modelling and further validated the influence of these inhibitors on nsp13 and viral entry. Interestingly, pralatrexate and trimetrexate showed superior effects in counteracting the viral infection compared to other DHFR inhibitors. Our results indicate that their higher activity is due to their polypharmacological and pleiotropic profile. These compounds can thus potentially give a clinical advantage in the management of SARS-CoV-2 infection in patients already treated with this class of drugs. |
format | Online Article Text |
id | pubmed-10221469 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-102214692023-05-28 DHFR Inhibitors Display a Pleiotropic Anti-Viral Activity against SARS-CoV-2: Insights into the Mechanisms of Action Iaconis, Daniela Caccuri, Francesca Manelfi, Candida Talarico, Carmine Bugatti, Antonella Filippini, Federica Zani, Alberto Novelli, Rubina Kuzikov, Maria Ellinger, Bernhard Gribbon, Philip Riecken, Kristoffer Esposito, Francesca Corona, Angela Tramontano, Enzo Beccari, Andrea Rosario Caruso, Arnaldo Allegretti, Marcello Viruses Article During the COVID-19 pandemic, drug repurposing represented an effective strategy to obtain quick answers to medical emergencies. Based on previous data on methotrexate (MTX), we evaluated the anti-viral activity of several DHFR inhibitors in two cell lines. We observed that this class of compounds showed a significant influence on the virus-induced cytopathic effect (CPE) partly attributed to the intrinsic anti-metabolic activity of these drugs, but also to a specific anti-viral function. To elucidate the molecular mechanisms, we took advantage of our EXSCALATE platform for in-silico molecular modelling and further validated the influence of these inhibitors on nsp13 and viral entry. Interestingly, pralatrexate and trimetrexate showed superior effects in counteracting the viral infection compared to other DHFR inhibitors. Our results indicate that their higher activity is due to their polypharmacological and pleiotropic profile. These compounds can thus potentially give a clinical advantage in the management of SARS-CoV-2 infection in patients already treated with this class of drugs. MDPI 2023-05-09 /pmc/articles/PMC10221469/ /pubmed/37243214 http://dx.doi.org/10.3390/v15051128 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Iaconis, Daniela Caccuri, Francesca Manelfi, Candida Talarico, Carmine Bugatti, Antonella Filippini, Federica Zani, Alberto Novelli, Rubina Kuzikov, Maria Ellinger, Bernhard Gribbon, Philip Riecken, Kristoffer Esposito, Francesca Corona, Angela Tramontano, Enzo Beccari, Andrea Rosario Caruso, Arnaldo Allegretti, Marcello DHFR Inhibitors Display a Pleiotropic Anti-Viral Activity against SARS-CoV-2: Insights into the Mechanisms of Action |
title | DHFR Inhibitors Display a Pleiotropic Anti-Viral Activity against SARS-CoV-2: Insights into the Mechanisms of Action |
title_full | DHFR Inhibitors Display a Pleiotropic Anti-Viral Activity against SARS-CoV-2: Insights into the Mechanisms of Action |
title_fullStr | DHFR Inhibitors Display a Pleiotropic Anti-Viral Activity against SARS-CoV-2: Insights into the Mechanisms of Action |
title_full_unstemmed | DHFR Inhibitors Display a Pleiotropic Anti-Viral Activity against SARS-CoV-2: Insights into the Mechanisms of Action |
title_short | DHFR Inhibitors Display a Pleiotropic Anti-Viral Activity against SARS-CoV-2: Insights into the Mechanisms of Action |
title_sort | dhfr inhibitors display a pleiotropic anti-viral activity against sars-cov-2: insights into the mechanisms of action |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10221469/ https://www.ncbi.nlm.nih.gov/pubmed/37243214 http://dx.doi.org/10.3390/v15051128 |
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