4.7 Article

Capivasertib restricts SARS-CoV-2 cellular entry: a potential clinical application for COVID-19

Journal

INTERNATIONAL JOURNAL OF BIOLOGICAL SCIENCES
Volume 17, Issue 9, Pages 2348-2355

Publisher

IVYSPRING INT PUBL
DOI: 10.7150/ijbs.57810

Keywords

COVID-19; SARS-CoV-2; AKT inhibitor; capivasertib; antiviral activity

Funding

  1. National Science Fund of China [31872239]
  2. Fundamental Research Fund for the Central Universities of China [2042021kf0219]
  3. Science and Technology Development Fund Macau SAR [0055/2019/A1]
  4. Hubei Science Fund for Excellent Scholars [2020CFA015]
  5. Nazarbayev University Faculty-Development Competitive Research Grants [15798117 (110119FD4531), 15874919 (110119FD4542)]

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The study identified the PI3K/AKT pathway as crucial in COVID-19, with inhibitors potentially blocking SARS-CoV-2 entry into cells and offering antiviral targets. This suggests that PI3K/AKT kinase inhibitor drugs could be a promising strategy for managing COVID-19, especially in cancer patients.
Coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection has led to more than 150 million infections and about 3.1 million deaths up to date. Currently, drugs screened are urgently aiming to block the infection of SARS-CoV-2. Here, we explored the interaction networks of kinase and COVID-19 crosstalk, and identified phosphoinositide 3-kinase (PI3K)/AKT pathway as the most important kinase signal pathway involving COVID-19. Further, we found a PI3K/AKT signal pathway inhibitor capivasertib restricted the entry of SARS-CoV-2 into cells under non-cytotoxic concentrations. Lastly, the signal axis PI3K/AKT/FYVE finger-containing phosphoinositide kinase (PIKfyve)/PtdIns(3,5)P2 was revealed to play a key role during the cellular entry of viruses including SARS-CoV-2, possibly providing potential antiviral targets. Altogether, our study suggests that the PI3K/AKT kinase inhibitor drugs may be a promising anti-SARS-CoV-2 strategy for clinical application, especially for managing cancer patients with COVID-19 in the pandemic era. Coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection has led to more than 150 million infections and about 3.1 million deaths up to date. Currently, drugs screened are urgently aiming to block the infection of SARS-CoV-2. Here, we explored the interaction networks of kinase and COVID-19 crosstalk, and identified phosphoinositide 3-kinase (PI3K)/AKT pathway as the most important kinase signal pathway involving COVID-19. Further, we found a PI3K/AKT signal pathway inhibitor capivasertib restricted the entry of SARS-CoV-2 into cells under non-cytotoxic concentrations. Lastly, the signal axis PI3K/AKT/FYVE finger-containing phosphoinositide kinase (PIKfyve)/PtdIns(3,5)P2 was revealed to play a key role during the cellular entry of viruses including SARS-CoV-2, possibly providing potential antiviral targets. Altogether, our study suggests that the PI3K/AKT kinase inhibitor drugs may be a promising anti-SARS-CoV-2 strategy for clinical application, especially for managing cancer patients with COVID-19 in the pandemic era.

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