Dolma Lobsang
GOF Mutant p53 in Cancers: A Therapeutic Challenge
Lobsang, Dolma; Muller, Patricia A.J.
Abstract
TP53 is mutated in the majority of human cancers. Mutations can lead to loss of p53 expression or expression of mutant versions of the p53 protein. These mutant p53 proteins have oncogenic potential. They can inhibit any remaining WTp53 in a dominant negative manner, or they can acquire new functions that promote tumour growth, invasion, metastasis and chemoresistance. In this review we explore some of the mechanisms that make mutant p53 cells resistant to chemotherapy. As mutant p53 tumours are resistant to many traditional chemotherapies, many have sought to explore new ways of targeting mutant p53 tumours and reinstate chemosensitivity. These approaches include targeting of mutant p53 stability, mutant p53 binding partners and downstream pathways, p53 vaccines, restoration of WTp53 function, and WTp53 gene delivery. The current advances and challenges of these strategies are discussed.
Citation
Lobsang, D., & Muller, P. A. (2022). GOF Mutant p53 in Cancers: A Therapeutic Challenge. Cancers, 14(20), Article 5091. https://doi.org/10.3390/cancers14205091
Journal Article Type | Article |
---|---|
Acceptance Date | Oct 14, 2022 |
Online Publication Date | Oct 18, 2022 |
Publication Date | Oct 2, 2022 |
Deposit Date | Oct 18, 2022 |
Publicly Available Date | Oct 18, 2022 |
Journal | Cancers |
Electronic ISSN | 2072-6694 |
Publisher | MDPI |
Peer Reviewed | Peer Reviewed |
Volume | 14 |
Issue | 20 |
Article Number | 5091 |
DOI | https://doi.org/10.3390/cancers14205091 |
Public URL | https://durham-repository.worktribe.com/output/1188581 |
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Copyright Statement
© 2022 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 (https://
creativecommons.org/licenses/by/
4.0/).
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