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Insights Into the Properties, Biological Functions, and Regulation of USP21
Deubiquitylating enzymes (DUBs) antagonize ubiquitination by removing ubiquitin from their substrates. The role of DUBs in controlling various physiological and pathological processes has been extensively studied, and some members of DUBs have been identified as potential therapeutic targets in dise...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9279671/ https://www.ncbi.nlm.nih.gov/pubmed/35846989 http://dx.doi.org/10.3389/fphar.2022.944089 |
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author | An, Tao Lu, Yanting Yan, Xu Hou, Jingjing |
author_facet | An, Tao Lu, Yanting Yan, Xu Hou, Jingjing |
author_sort | An, Tao |
collection | PubMed |
description | Deubiquitylating enzymes (DUBs) antagonize ubiquitination by removing ubiquitin from their substrates. The role of DUBs in controlling various physiological and pathological processes has been extensively studied, and some members of DUBs have been identified as potential therapeutic targets in diseases ranging from tumors to neurodegeneration. Ubiquitin-specific protease 21 (USP21) is a member of the ubiquitin-specific protease family, the largest subfamily of DUBs. Although USP21 was discovered late and early research progress was slow, numerous studies in the last decade have gradually revealed the importance of USP21 in a wide variety of biological processes. In particular, the pro-carcinogenic effect of USP21 has been well elucidated in the last 2 years. In the present review, we provide a comprehensive overview of the current knowledge on USP21, including its properties, biological functions, pathophysiological roles, and cellular regulation. Limited pharmacological interventions for USP21 have also been introduced, highlighting the importance of developing novel and specific inhibitors targeting USP21. |
format | Online Article Text |
id | pubmed-9279671 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92796712022-07-15 Insights Into the Properties, Biological Functions, and Regulation of USP21 An, Tao Lu, Yanting Yan, Xu Hou, Jingjing Front Pharmacol Pharmacology Deubiquitylating enzymes (DUBs) antagonize ubiquitination by removing ubiquitin from their substrates. The role of DUBs in controlling various physiological and pathological processes has been extensively studied, and some members of DUBs have been identified as potential therapeutic targets in diseases ranging from tumors to neurodegeneration. Ubiquitin-specific protease 21 (USP21) is a member of the ubiquitin-specific protease family, the largest subfamily of DUBs. Although USP21 was discovered late and early research progress was slow, numerous studies in the last decade have gradually revealed the importance of USP21 in a wide variety of biological processes. In particular, the pro-carcinogenic effect of USP21 has been well elucidated in the last 2 years. In the present review, we provide a comprehensive overview of the current knowledge on USP21, including its properties, biological functions, pathophysiological roles, and cellular regulation. Limited pharmacological interventions for USP21 have also been introduced, highlighting the importance of developing novel and specific inhibitors targeting USP21. Frontiers Media S.A. 2022-06-30 /pmc/articles/PMC9279671/ /pubmed/35846989 http://dx.doi.org/10.3389/fphar.2022.944089 Text en Copyright © 2022 An, Lu, Yan and Hou. 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 An, Tao Lu, Yanting Yan, Xu Hou, Jingjing Insights Into the Properties, Biological Functions, and Regulation of USP21 |
title | Insights Into the Properties, Biological Functions, and Regulation of USP21 |
title_full | Insights Into the Properties, Biological Functions, and Regulation of USP21 |
title_fullStr | Insights Into the Properties, Biological Functions, and Regulation of USP21 |
title_full_unstemmed | Insights Into the Properties, Biological Functions, and Regulation of USP21 |
title_short | Insights Into the Properties, Biological Functions, and Regulation of USP21 |
title_sort | insights into the properties, biological functions, and regulation of usp21 |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9279671/ https://www.ncbi.nlm.nih.gov/pubmed/35846989 http://dx.doi.org/10.3389/fphar.2022.944089 |
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