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SARS-CoV-2 infection: can ferroptosis be a potential treatment target for multiple organ involvement?

Since the outbreak of the new coronavirus in 2019 (SARS-CoV-2), many studies have been performed to better understand the basic mechanisms and clinical features of the disease. However, uncertainties of the underlying mechanisms of multiple organ involvement remain. A substantial proportion of sever...

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Autores principales: Yang, Ming, Lai, Ching Lung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7687212/
https://www.ncbi.nlm.nih.gov/pubmed/33251029
http://dx.doi.org/10.1038/s41420-020-00369-w
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author Yang, Ming
Lai, Ching Lung
author_facet Yang, Ming
Lai, Ching Lung
author_sort Yang, Ming
collection PubMed
description Since the outbreak of the new coronavirus in 2019 (SARS-CoV-2), many studies have been performed to better understand the basic mechanisms and clinical features of the disease. However, uncertainties of the underlying mechanisms of multiple organ involvement remain. A substantial proportion of severe coronavirus disease 2019 (COVID-19) patients have lymphopenia, low serum iron levels, and multiple organ involvement. Several therapeutic agents have been used for different stages of the disease, but the treatment for severe disease is still suboptimal. Understanding the mechanism of programmed cell death in COVID-19 may lead to better therapeutic strategies for these patients. On the basis of observations of basic science studies and clinical researches on COVID-19, we hypothesize that ferroptosis, a novel programmed cell death, may be an important cause of multiple organ involvement in COVID-19 and it might serve as a new treatment target. In spite of the existing findings on the involvement of ferroptosis in SARS-CoV-2 infection, there is no reported study to uncover how does ferroptosis acts in SARS-CoV-2 infection yet. Uncovering the role of ferroptosis in SARS-CoV-2 infection is essential to develop new treatment strategies for COVID-19. Intracellular cell iron depletion or new generation of ferroptosis inhibitors might be potential drug candidates for COVID-19. We hope this hypothesis may launch a new wave of studies to uncover the association of ferroptosis and SARS-CoV-2 infection in vitro and in vivo.
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spelling pubmed-76872122020-11-25 SARS-CoV-2 infection: can ferroptosis be a potential treatment target for multiple organ involvement? Yang, Ming Lai, Ching Lung Cell Death Discov Perspective Since the outbreak of the new coronavirus in 2019 (SARS-CoV-2), many studies have been performed to better understand the basic mechanisms and clinical features of the disease. However, uncertainties of the underlying mechanisms of multiple organ involvement remain. A substantial proportion of severe coronavirus disease 2019 (COVID-19) patients have lymphopenia, low serum iron levels, and multiple organ involvement. Several therapeutic agents have been used for different stages of the disease, but the treatment for severe disease is still suboptimal. Understanding the mechanism of programmed cell death in COVID-19 may lead to better therapeutic strategies for these patients. On the basis of observations of basic science studies and clinical researches on COVID-19, we hypothesize that ferroptosis, a novel programmed cell death, may be an important cause of multiple organ involvement in COVID-19 and it might serve as a new treatment target. In spite of the existing findings on the involvement of ferroptosis in SARS-CoV-2 infection, there is no reported study to uncover how does ferroptosis acts in SARS-CoV-2 infection yet. Uncovering the role of ferroptosis in SARS-CoV-2 infection is essential to develop new treatment strategies for COVID-19. Intracellular cell iron depletion or new generation of ferroptosis inhibitors might be potential drug candidates for COVID-19. We hope this hypothesis may launch a new wave of studies to uncover the association of ferroptosis and SARS-CoV-2 infection in vitro and in vivo. Nature Publishing Group UK 2020-11-25 /pmc/articles/PMC7687212/ /pubmed/33251029 http://dx.doi.org/10.1038/s41420-020-00369-w Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Perspective
Yang, Ming
Lai, Ching Lung
SARS-CoV-2 infection: can ferroptosis be a potential treatment target for multiple organ involvement?
title SARS-CoV-2 infection: can ferroptosis be a potential treatment target for multiple organ involvement?
title_full SARS-CoV-2 infection: can ferroptosis be a potential treatment target for multiple organ involvement?
title_fullStr SARS-CoV-2 infection: can ferroptosis be a potential treatment target for multiple organ involvement?
title_full_unstemmed SARS-CoV-2 infection: can ferroptosis be a potential treatment target for multiple organ involvement?
title_short SARS-CoV-2 infection: can ferroptosis be a potential treatment target for multiple organ involvement?
title_sort sars-cov-2 infection: can ferroptosis be a potential treatment target for multiple organ involvement?
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7687212/
https://www.ncbi.nlm.nih.gov/pubmed/33251029
http://dx.doi.org/10.1038/s41420-020-00369-w
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