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The Janus Face of p53-Targeting Ubiquitin Ligases

The tumor suppressor p53 prevents tumorigenesis and cancer progression by maintaining genomic stability and inducing cell growth arrest and apoptosis. Because of the extremely detrimental nature of wild-type p53, cancer cells usually mutate the TP53 gene in favor of their survival and propagation. S...

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Detalles Bibliográficos
Autores principales: Hao, Qian, Chen, Yajie, Zhou, Xiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7407405/
https://www.ncbi.nlm.nih.gov/pubmed/32660118
http://dx.doi.org/10.3390/cells9071656
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author Hao, Qian
Chen, Yajie
Zhou, Xiang
author_facet Hao, Qian
Chen, Yajie
Zhou, Xiang
author_sort Hao, Qian
collection PubMed
description The tumor suppressor p53 prevents tumorigenesis and cancer progression by maintaining genomic stability and inducing cell growth arrest and apoptosis. Because of the extremely detrimental nature of wild-type p53, cancer cells usually mutate the TP53 gene in favor of their survival and propagation. Some of the mutant p53 proteins not only lose the wild-type activity, but also acquire oncogenic function, namely “gain-of-function”, to promote cancer development. Growing evidence has revealed that various E3 ubiquitin ligases are able to target both wild-type and mutant p53 for degradation or inactivation, and thus play divergent roles leading to cancer cell survival or death in the context of different p53 status. In this essay, we reviewed the recent progress in our understanding of the p53-targeting E3 ubiquitin ligases, and discussed the potential clinical implications of these E3 ubiquitin ligases in cancer therapy.
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spelling pubmed-74074052020-08-25 The Janus Face of p53-Targeting Ubiquitin Ligases Hao, Qian Chen, Yajie Zhou, Xiang Cells Review The tumor suppressor p53 prevents tumorigenesis and cancer progression by maintaining genomic stability and inducing cell growth arrest and apoptosis. Because of the extremely detrimental nature of wild-type p53, cancer cells usually mutate the TP53 gene in favor of their survival and propagation. Some of the mutant p53 proteins not only lose the wild-type activity, but also acquire oncogenic function, namely “gain-of-function”, to promote cancer development. Growing evidence has revealed that various E3 ubiquitin ligases are able to target both wild-type and mutant p53 for degradation or inactivation, and thus play divergent roles leading to cancer cell survival or death in the context of different p53 status. In this essay, we reviewed the recent progress in our understanding of the p53-targeting E3 ubiquitin ligases, and discussed the potential clinical implications of these E3 ubiquitin ligases in cancer therapy. MDPI 2020-07-09 /pmc/articles/PMC7407405/ /pubmed/32660118 http://dx.doi.org/10.3390/cells9071656 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Hao, Qian
Chen, Yajie
Zhou, Xiang
The Janus Face of p53-Targeting Ubiquitin Ligases
title The Janus Face of p53-Targeting Ubiquitin Ligases
title_full The Janus Face of p53-Targeting Ubiquitin Ligases
title_fullStr The Janus Face of p53-Targeting Ubiquitin Ligases
title_full_unstemmed The Janus Face of p53-Targeting Ubiquitin Ligases
title_short The Janus Face of p53-Targeting Ubiquitin Ligases
title_sort janus face of p53-targeting ubiquitin ligases
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7407405/
https://www.ncbi.nlm.nih.gov/pubmed/32660118
http://dx.doi.org/10.3390/cells9071656
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