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The Emerging Role of Deubiquitinases in Cell Death

Regulated cell death (RCD) is a signal-controlled process that not only eliminates infected, damaged, or aged cells but is also implicated in a variety of pathological conditions. The process of RCD is regulated by intracellular proteins that undergo varying levels of post-translational modification...

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Autores principales: Zhou, Zhuan, Song, Xinxin, Kang, Rui, Tang, Daolin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9775562/
https://www.ncbi.nlm.nih.gov/pubmed/36551253
http://dx.doi.org/10.3390/biom12121825
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author Zhou, Zhuan
Song, Xinxin
Kang, Rui
Tang, Daolin
author_facet Zhou, Zhuan
Song, Xinxin
Kang, Rui
Tang, Daolin
author_sort Zhou, Zhuan
collection PubMed
description Regulated cell death (RCD) is a signal-controlled process that not only eliminates infected, damaged, or aged cells but is also implicated in a variety of pathological conditions. The process of RCD is regulated by intracellular proteins that undergo varying levels of post-translational modifications, including mono- or polyubiquitination. Functionally, ubiquitination can affect protein abundance, localization, and activity. Like other post-translational modifications, ubiquitination is a dynamic and reversible process mediated by deubiquitinases, a large class of proteases that cleave ubiquitin from proteins and other substrates. The balance between ubiquitination and deubiquitination machinery determines cell fate under stressful conditions. Here, we review the latest advances in our understanding of the role of deubiquitinases in regulating the main types of RCD, including apoptosis, necroptosis, pyroptosis, and ferroptosis. This knowledge may contribute to identifying new protein degradation-related prognostic markers and therapeutic targets for human disease.
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spelling pubmed-97755622022-12-23 The Emerging Role of Deubiquitinases in Cell Death Zhou, Zhuan Song, Xinxin Kang, Rui Tang, Daolin Biomolecules Review Regulated cell death (RCD) is a signal-controlled process that not only eliminates infected, damaged, or aged cells but is also implicated in a variety of pathological conditions. The process of RCD is regulated by intracellular proteins that undergo varying levels of post-translational modifications, including mono- or polyubiquitination. Functionally, ubiquitination can affect protein abundance, localization, and activity. Like other post-translational modifications, ubiquitination is a dynamic and reversible process mediated by deubiquitinases, a large class of proteases that cleave ubiquitin from proteins and other substrates. The balance between ubiquitination and deubiquitination machinery determines cell fate under stressful conditions. Here, we review the latest advances in our understanding of the role of deubiquitinases in regulating the main types of RCD, including apoptosis, necroptosis, pyroptosis, and ferroptosis. This knowledge may contribute to identifying new protein degradation-related prognostic markers and therapeutic targets for human disease. MDPI 2022-12-06 /pmc/articles/PMC9775562/ /pubmed/36551253 http://dx.doi.org/10.3390/biom12121825 Text en © 2022 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 Review
Zhou, Zhuan
Song, Xinxin
Kang, Rui
Tang, Daolin
The Emerging Role of Deubiquitinases in Cell Death
title The Emerging Role of Deubiquitinases in Cell Death
title_full The Emerging Role of Deubiquitinases in Cell Death
title_fullStr The Emerging Role of Deubiquitinases in Cell Death
title_full_unstemmed The Emerging Role of Deubiquitinases in Cell Death
title_short The Emerging Role of Deubiquitinases in Cell Death
title_sort emerging role of deubiquitinases in cell death
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9775562/
https://www.ncbi.nlm.nih.gov/pubmed/36551253
http://dx.doi.org/10.3390/biom12121825
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