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Targeting deubiquitinase USP28 for cancer therapy

As one of the most important post-translational modifications, ubiquitination plays versatile roles in cancer-related pathways, and is involved in protein metabolism, cell-cycle progression, apoptosis, and transcription. Counteracting the activities of the E3 ligases, the deubiquitylating enzymes ha...

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Autores principales: Wang, Xiaofang, Liu, Zhiyi, Zhang, Li, Yang, Zhaozhi, Chen, Xingxing, Luo, Jurui, Zhou, Zhirui, Mei, Xin, Yu, Xiaoli, Shao, Zhimin, Feng, Yan, Fu, Shen, Zhang, Zhen, Wei, Dongping, Jia, Lijun, Ma, Jinli, Guo, Xiaomao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833459/
https://www.ncbi.nlm.nih.gov/pubmed/29415985
http://dx.doi.org/10.1038/s41419-017-0208-z
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author Wang, Xiaofang
Liu, Zhiyi
Zhang, Li
Yang, Zhaozhi
Chen, Xingxing
Luo, Jurui
Zhou, Zhirui
Mei, Xin
Yu, Xiaoli
Shao, Zhimin
Feng, Yan
Fu, Shen
Zhang, Zhen
Wei, Dongping
Jia, Lijun
Ma, Jinli
Guo, Xiaomao
author_facet Wang, Xiaofang
Liu, Zhiyi
Zhang, Li
Yang, Zhaozhi
Chen, Xingxing
Luo, Jurui
Zhou, Zhirui
Mei, Xin
Yu, Xiaoli
Shao, Zhimin
Feng, Yan
Fu, Shen
Zhang, Zhen
Wei, Dongping
Jia, Lijun
Ma, Jinli
Guo, Xiaomao
author_sort Wang, Xiaofang
collection PubMed
description As one of the most important post-translational modifications, ubiquitination plays versatile roles in cancer-related pathways, and is involved in protein metabolism, cell-cycle progression, apoptosis, and transcription. Counteracting the activities of the E3 ligases, the deubiquitylating enzymes have been suggested as another important mechanism to modulate the ubiquitination process, and are implicated in cancer as well. In this article, we review the emerging roles of USP28 in cancer pathways as revealed by recent studies. We discuss the major mechanisms by which USP28 is involved in the cancer-related pathways, whereby USP28 regulates physiological homeostasis of ubiquitination process, DNA-damage response, and cell cycle during genotoxic stress. We further review the studies where USP28 was targeted for treating multiples cancers including non-small cell lung cancer, breast cancer, intestinal cancers, gliomas, and bladder cancer. As a result, the clinical significance of targeting USP28 for cancer therapy merits further exploration and demonstration.
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spelling pubmed-58334592018-03-05 Targeting deubiquitinase USP28 for cancer therapy Wang, Xiaofang Liu, Zhiyi Zhang, Li Yang, Zhaozhi Chen, Xingxing Luo, Jurui Zhou, Zhirui Mei, Xin Yu, Xiaoli Shao, Zhimin Feng, Yan Fu, Shen Zhang, Zhen Wei, Dongping Jia, Lijun Ma, Jinli Guo, Xiaomao Cell Death Dis Review Article As one of the most important post-translational modifications, ubiquitination plays versatile roles in cancer-related pathways, and is involved in protein metabolism, cell-cycle progression, apoptosis, and transcription. Counteracting the activities of the E3 ligases, the deubiquitylating enzymes have been suggested as another important mechanism to modulate the ubiquitination process, and are implicated in cancer as well. In this article, we review the emerging roles of USP28 in cancer pathways as revealed by recent studies. We discuss the major mechanisms by which USP28 is involved in the cancer-related pathways, whereby USP28 regulates physiological homeostasis of ubiquitination process, DNA-damage response, and cell cycle during genotoxic stress. We further review the studies where USP28 was targeted for treating multiples cancers including non-small cell lung cancer, breast cancer, intestinal cancers, gliomas, and bladder cancer. As a result, the clinical significance of targeting USP28 for cancer therapy merits further exploration and demonstration. Nature Publishing Group UK 2018-02-07 /pmc/articles/PMC5833459/ /pubmed/29415985 http://dx.doi.org/10.1038/s41419-017-0208-z Text en © The Author(s) 2018 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 Review Article
Wang, Xiaofang
Liu, Zhiyi
Zhang, Li
Yang, Zhaozhi
Chen, Xingxing
Luo, Jurui
Zhou, Zhirui
Mei, Xin
Yu, Xiaoli
Shao, Zhimin
Feng, Yan
Fu, Shen
Zhang, Zhen
Wei, Dongping
Jia, Lijun
Ma, Jinli
Guo, Xiaomao
Targeting deubiquitinase USP28 for cancer therapy
title Targeting deubiquitinase USP28 for cancer therapy
title_full Targeting deubiquitinase USP28 for cancer therapy
title_fullStr Targeting deubiquitinase USP28 for cancer therapy
title_full_unstemmed Targeting deubiquitinase USP28 for cancer therapy
title_short Targeting deubiquitinase USP28 for cancer therapy
title_sort targeting deubiquitinase usp28 for cancer therapy
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833459/
https://www.ncbi.nlm.nih.gov/pubmed/29415985
http://dx.doi.org/10.1038/s41419-017-0208-z
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