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The Role of Deubiquitinases in Oncovirus and Host Interactions

Infection-related cancer comprises one-sixth of the global cancer burden. Oncoviruses can directly or indirectly contribute to tumorigenesis. Ubiquitination is a dynamic and reversible posttranslational modification that participates in almost all cellular processes. Hijacking of the ubiquitin syste...

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Autores principales: Li, Yueshuo, Shi, Feng, Hu, Jianmin, Xie, Longlong, Bode, Ann M., Cao, Ya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6668545/
https://www.ncbi.nlm.nih.gov/pubmed/31396277
http://dx.doi.org/10.1155/2019/2128410
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author Li, Yueshuo
Shi, Feng
Hu, Jianmin
Xie, Longlong
Bode, Ann M.
Cao, Ya
author_facet Li, Yueshuo
Shi, Feng
Hu, Jianmin
Xie, Longlong
Bode, Ann M.
Cao, Ya
author_sort Li, Yueshuo
collection PubMed
description Infection-related cancer comprises one-sixth of the global cancer burden. Oncoviruses can directly or indirectly contribute to tumorigenesis. Ubiquitination is a dynamic and reversible posttranslational modification that participates in almost all cellular processes. Hijacking of the ubiquitin system by viruses continues to emerge as a central theme around the viral life cycle. Deubiquitinating enzymes (DUBs) maintain ubiquitin homeostasis by removing ubiquitin modifications from target proteins, thereby altering protein function, stability, and signaling pathways, as well as acting as key mediators between the virus and its host. In this review, we focus on the multiple functions of DUBs in RIG-I-like receptors (RLRs) and stimulator of interferon genes (STING)-mediated antiviral signaling pathways, oncoviruses regulation of NF-κB activation, oncoviral life cycle, and the potential of DUB inhibitors as therapeutic strategies.
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spelling pubmed-66685452019-08-08 The Role of Deubiquitinases in Oncovirus and Host Interactions Li, Yueshuo Shi, Feng Hu, Jianmin Xie, Longlong Bode, Ann M. Cao, Ya J Oncol Review Article Infection-related cancer comprises one-sixth of the global cancer burden. Oncoviruses can directly or indirectly contribute to tumorigenesis. Ubiquitination is a dynamic and reversible posttranslational modification that participates in almost all cellular processes. Hijacking of the ubiquitin system by viruses continues to emerge as a central theme around the viral life cycle. Deubiquitinating enzymes (DUBs) maintain ubiquitin homeostasis by removing ubiquitin modifications from target proteins, thereby altering protein function, stability, and signaling pathways, as well as acting as key mediators between the virus and its host. In this review, we focus on the multiple functions of DUBs in RIG-I-like receptors (RLRs) and stimulator of interferon genes (STING)-mediated antiviral signaling pathways, oncoviruses regulation of NF-κB activation, oncoviral life cycle, and the potential of DUB inhibitors as therapeutic strategies. Hindawi 2019-07-18 /pmc/articles/PMC6668545/ /pubmed/31396277 http://dx.doi.org/10.1155/2019/2128410 Text en Copyright © 2019 Yueshuo Li et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Li, Yueshuo
Shi, Feng
Hu, Jianmin
Xie, Longlong
Bode, Ann M.
Cao, Ya
The Role of Deubiquitinases in Oncovirus and Host Interactions
title The Role of Deubiquitinases in Oncovirus and Host Interactions
title_full The Role of Deubiquitinases in Oncovirus and Host Interactions
title_fullStr The Role of Deubiquitinases in Oncovirus and Host Interactions
title_full_unstemmed The Role of Deubiquitinases in Oncovirus and Host Interactions
title_short The Role of Deubiquitinases in Oncovirus and Host Interactions
title_sort role of deubiquitinases in oncovirus and host interactions
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6668545/
https://www.ncbi.nlm.nih.gov/pubmed/31396277
http://dx.doi.org/10.1155/2019/2128410
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