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Gasdermin E: A Prospective Target for Therapy of Diseases

Gasdermin E (GSDME) is a member of the gasdermin protein family, which mediates programmed cell death including apoptosis and pyroptosis. Recently, it was suggested that GSDME is activated by chemotherapeutic drugs to stimulate pyroptosis of cancer cells and trigger anti-tumor immunity, which is ide...

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Autores principales: Liao, Xiu-Xiu, Dai, Yong-Zhao, Zhao, Yao-Zhong, Nie, Ke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9019550/
https://www.ncbi.nlm.nih.gov/pubmed/35462927
http://dx.doi.org/10.3389/fphar.2022.855828
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author Liao, Xiu-Xiu
Dai, Yong-Zhao
Zhao, Yao-Zhong
Nie, Ke
author_facet Liao, Xiu-Xiu
Dai, Yong-Zhao
Zhao, Yao-Zhong
Nie, Ke
author_sort Liao, Xiu-Xiu
collection PubMed
description Gasdermin E (GSDME) is a member of the gasdermin protein family, which mediates programmed cell death including apoptosis and pyroptosis. Recently, it was suggested that GSDME is activated by chemotherapeutic drugs to stimulate pyroptosis of cancer cells and trigger anti-tumor immunity, which is identified as a tumor suppressor. However, GSDME-mediated pyroptosis contributes to normal tissue damage, leading to pathological inflammations. Inhibiting GSDME-mediated pyroptosis might be a potential target in ameliorating inflammatory diseases. Therefore, targeting GSDME is a promising option for the treatment of diseases in the future. In this review, we introduce the roles of GSDME-driven programmed cell death in different diseases and the potential targeted therapies of GSDME, so as to provide a foundation for future research.
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spelling pubmed-90195502022-04-21 Gasdermin E: A Prospective Target for Therapy of Diseases Liao, Xiu-Xiu Dai, Yong-Zhao Zhao, Yao-Zhong Nie, Ke Front Pharmacol Pharmacology Gasdermin E (GSDME) is a member of the gasdermin protein family, which mediates programmed cell death including apoptosis and pyroptosis. Recently, it was suggested that GSDME is activated by chemotherapeutic drugs to stimulate pyroptosis of cancer cells and trigger anti-tumor immunity, which is identified as a tumor suppressor. However, GSDME-mediated pyroptosis contributes to normal tissue damage, leading to pathological inflammations. Inhibiting GSDME-mediated pyroptosis might be a potential target in ameliorating inflammatory diseases. Therefore, targeting GSDME is a promising option for the treatment of diseases in the future. In this review, we introduce the roles of GSDME-driven programmed cell death in different diseases and the potential targeted therapies of GSDME, so as to provide a foundation for future research. Frontiers Media S.A. 2022-04-06 /pmc/articles/PMC9019550/ /pubmed/35462927 http://dx.doi.org/10.3389/fphar.2022.855828 Text en Copyright © 2022 Liao, Dai, Zhao and Nie. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Liao, Xiu-Xiu
Dai, Yong-Zhao
Zhao, Yao-Zhong
Nie, Ke
Gasdermin E: A Prospective Target for Therapy of Diseases
title Gasdermin E: A Prospective Target for Therapy of Diseases
title_full Gasdermin E: A Prospective Target for Therapy of Diseases
title_fullStr Gasdermin E: A Prospective Target for Therapy of Diseases
title_full_unstemmed Gasdermin E: A Prospective Target for Therapy of Diseases
title_short Gasdermin E: A Prospective Target for Therapy of Diseases
title_sort gasdermin e: a prospective target for therapy of diseases
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9019550/
https://www.ncbi.nlm.nih.gov/pubmed/35462927
http://dx.doi.org/10.3389/fphar.2022.855828
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