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Mutant p53 in cancer: from molecular mechanism to therapeutic modulation
TP53, a crucial tumor suppressor gene, is the most commonly mutated gene in human cancers. Aside from losing its tumor suppressor function, mutant p53 (mutp53) often acquires inherent, novel oncogenic functions, which is termed “gain-of-function”. Emerging evidence suggests that mutp53 is highly ass...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9674619/ https://www.ncbi.nlm.nih.gov/pubmed/36400749 http://dx.doi.org/10.1038/s41419-022-05408-1 |
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author | Chen, Xiaohua Zhang, Taotao Su, Wei Dou, Zhihui Zhao, Dapeng Jin, Xiaodong Lei, Huiwen Wang, Jing Xie, Xiaodong Cheng, Bo Li, Qiang Zhang, Hong Di, Cuixia |
author_facet | Chen, Xiaohua Zhang, Taotao Su, Wei Dou, Zhihui Zhao, Dapeng Jin, Xiaodong Lei, Huiwen Wang, Jing Xie, Xiaodong Cheng, Bo Li, Qiang Zhang, Hong Di, Cuixia |
author_sort | Chen, Xiaohua |
collection | PubMed |
description | TP53, a crucial tumor suppressor gene, is the most commonly mutated gene in human cancers. Aside from losing its tumor suppressor function, mutant p53 (mutp53) often acquires inherent, novel oncogenic functions, which is termed “gain-of-function”. Emerging evidence suggests that mutp53 is highly associated with advanced malignancies and poor prognosis, which makes it a target for development of novel cancer therapies. Herein, we provide a summary of our knowledge of the mutp53 types and mutp53 spectrum in cancers. The mechanisms of mutp53 accumulation and gain-of-function are also summarized. Furthermore, we discuss the gain-of-function of mutp53 in cancers: genetic instability, ferroptosis, microenvironment, and stemness. Importantly, the role of mutp53 in the clinic is also discussed, particularly with regard to chemotherapy and radiotherapy. Last, emphasis is given to emerging strategies on how to target mutp53 for tumor therapy. Thus, this review will contribute to better understanding of the significance of mutp53 as a target for therapeutic strategies. |
format | Online Article Text |
id | pubmed-9674619 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96746192022-11-20 Mutant p53 in cancer: from molecular mechanism to therapeutic modulation Chen, Xiaohua Zhang, Taotao Su, Wei Dou, Zhihui Zhao, Dapeng Jin, Xiaodong Lei, Huiwen Wang, Jing Xie, Xiaodong Cheng, Bo Li, Qiang Zhang, Hong Di, Cuixia Cell Death Dis Review Article TP53, a crucial tumor suppressor gene, is the most commonly mutated gene in human cancers. Aside from losing its tumor suppressor function, mutant p53 (mutp53) often acquires inherent, novel oncogenic functions, which is termed “gain-of-function”. Emerging evidence suggests that mutp53 is highly associated with advanced malignancies and poor prognosis, which makes it a target for development of novel cancer therapies. Herein, we provide a summary of our knowledge of the mutp53 types and mutp53 spectrum in cancers. The mechanisms of mutp53 accumulation and gain-of-function are also summarized. Furthermore, we discuss the gain-of-function of mutp53 in cancers: genetic instability, ferroptosis, microenvironment, and stemness. Importantly, the role of mutp53 in the clinic is also discussed, particularly with regard to chemotherapy and radiotherapy. Last, emphasis is given to emerging strategies on how to target mutp53 for tumor therapy. Thus, this review will contribute to better understanding of the significance of mutp53 as a target for therapeutic strategies. Nature Publishing Group UK 2022-11-18 /pmc/articles/PMC9674619/ /pubmed/36400749 http://dx.doi.org/10.1038/s41419-022-05408-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Article Chen, Xiaohua Zhang, Taotao Su, Wei Dou, Zhihui Zhao, Dapeng Jin, Xiaodong Lei, Huiwen Wang, Jing Xie, Xiaodong Cheng, Bo Li, Qiang Zhang, Hong Di, Cuixia Mutant p53 in cancer: from molecular mechanism to therapeutic modulation |
title | Mutant p53 in cancer: from molecular mechanism to therapeutic modulation |
title_full | Mutant p53 in cancer: from molecular mechanism to therapeutic modulation |
title_fullStr | Mutant p53 in cancer: from molecular mechanism to therapeutic modulation |
title_full_unstemmed | Mutant p53 in cancer: from molecular mechanism to therapeutic modulation |
title_short | Mutant p53 in cancer: from molecular mechanism to therapeutic modulation |
title_sort | mutant p53 in cancer: from molecular mechanism to therapeutic modulation |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9674619/ https://www.ncbi.nlm.nih.gov/pubmed/36400749 http://dx.doi.org/10.1038/s41419-022-05408-1 |
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