pandemic is caused by the SARS-CoV-2 virus, whose internalization and infection are mediated by the angiotensin-converting enzyme 2 (ACE2). The identification of novel approaches to tackle this step is instrumental for the development of therapies for the management of COVID-19 and other diseases with a similar mechanism of infection. Thalidomide, a drug sadly known for its teratogenic effects, has potent immunomodulatory and anti-inflammatory properties. Treatment with this drug has been shown to improve the immune functions of COVID-19 patients and proposed for the management of COVID-19 in clinical practice through drug repositioning. Here, we investigated the molecular details linking thalidomide to ACE2 and COVID-19, showing that in conditions mimicking SARS-CoV-2-associated cytokine storm, the transcription factor Delta Np63 alpha and ACE2 are stabilized, and IL-8 production is increased. In such conditions, we found p63 to bind to and regulate the expression of the ACE2 gene. We previously showed that Delta Np63 alpha is degraded upon thalidomide treatment and now found that treatment with this drug-or with its analogue lenalidomide-downregulates ACE2 in a p63-dependent manner. Finally, we found that thalidomide treatment reduces in vitro infection by pseudo-SARS-CoV-2, a baculovirus pseudotyped with the SARS-CoV-2 spike protein. Overall, we propose the dual effect of thalidomide in reducing SARS-CoV-2 viral re-entry and inflammation through p63 degradation to weaken SARS-CoV-2 entry into host cells and mitigate lung inflammation, making it a valuable option in clinical management of COVID-19.Key messagesThalidomide treatment results in p63-dependent ACE2 downregulation.ACE2 is a p63 transcriptional target.Thalidomide reduces the "cytokine storm" associated to COVID-19.Thalidomide prevents viral re-entry of SARS-CoV-2 by p63-dependent ACE2 downregulation.Thalidomide is a modulator of SARS-CoV-2 or other ACE2-dependent infections.ACE2 is modulated by a pharmacological substance.

Molecular mechanisms of thalidomide effectiveness on COVID-19 patients explained: ACE2 is a new ΔNp63α target gene / L. Monteonofrio, I. Virdia, S. Pozzi, R. Quadri, A. Amendolare, F. Marzano, M. Braile, V. Sulfaro, M. Paroni, A. Tullo, S. Soddu, L. Guerrini. - In: JOURNAL OF MOLECULAR MEDICINE. - ISSN 0946-2716. - (2024), pp. 1-10. [Epub ahead of print] [10.1007/s00109-024-02485-x]

Molecular mechanisms of thalidomide effectiveness on COVID-19 patients explained: ACE2 is a new ΔNp63α target gene

R. Quadri
Membro del Collaboration Group
;
F. Marzano
Membro del Collaboration Group
;
M. Braile
Membro del Collaboration Group
;
M. Paroni
Membro del Collaboration Group
;
L. Guerrini
Co-ultimo
Membro del Collaboration Group
2024

Abstract

pandemic is caused by the SARS-CoV-2 virus, whose internalization and infection are mediated by the angiotensin-converting enzyme 2 (ACE2). The identification of novel approaches to tackle this step is instrumental for the development of therapies for the management of COVID-19 and other diseases with a similar mechanism of infection. Thalidomide, a drug sadly known for its teratogenic effects, has potent immunomodulatory and anti-inflammatory properties. Treatment with this drug has been shown to improve the immune functions of COVID-19 patients and proposed for the management of COVID-19 in clinical practice through drug repositioning. Here, we investigated the molecular details linking thalidomide to ACE2 and COVID-19, showing that in conditions mimicking SARS-CoV-2-associated cytokine storm, the transcription factor Delta Np63 alpha and ACE2 are stabilized, and IL-8 production is increased. In such conditions, we found p63 to bind to and regulate the expression of the ACE2 gene. We previously showed that Delta Np63 alpha is degraded upon thalidomide treatment and now found that treatment with this drug-or with its analogue lenalidomide-downregulates ACE2 in a p63-dependent manner. Finally, we found that thalidomide treatment reduces in vitro infection by pseudo-SARS-CoV-2, a baculovirus pseudotyped with the SARS-CoV-2 spike protein. Overall, we propose the dual effect of thalidomide in reducing SARS-CoV-2 viral re-entry and inflammation through p63 degradation to weaken SARS-CoV-2 entry into host cells and mitigate lung inflammation, making it a valuable option in clinical management of COVID-19.Key messagesThalidomide treatment results in p63-dependent ACE2 downregulation.ACE2 is a p63 transcriptional target.Thalidomide reduces the "cytokine storm" associated to COVID-19.Thalidomide prevents viral re-entry of SARS-CoV-2 by p63-dependent ACE2 downregulation.Thalidomide is a modulator of SARS-CoV-2 or other ACE2-dependent infections.ACE2 is modulated by a pharmacological substance.
ACE2; COVID 19; SARS-CoV-2; Thalidomide; ΔNp63α
Settore BIOS-08/A - Biologia molecolare
   Psoriatic plaque as a tumor suppressor model: identification of cellular and inflammatory pathways leading to cancer prevention.
   MINISTERO DELL'UNIVERSITA' E DELLA RICERCA
   2022J2XH2S_002
2024
18-set-2024
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1103828
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