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GOF Mutant P53 in Cancers: A Therapeutic Challenge

Overview
Journal Cancers (Basel)
Publisher MDPI
Specialty Oncology
Date 2022 Oct 27
PMID 36291874
Authors
Affiliations
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Abstract

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.

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References
1.
OShea C, Soria C, Bagus B, McCormick F . Heat shock phenocopies E1B-55K late functions and selectively sensitizes refractory tumor cells to ONYX-015 oncolytic viral therapy. Cancer Cell. 2005; 8(1):61-74. DOI: 10.1016/j.ccr.2005.06.009. View

2.
Bykov V, Eriksson S, Bianchi J, Wiman K . Targeting mutant p53 for efficient cancer therapy. Nat Rev Cancer. 2017; 18(2):89-102. DOI: 10.1038/nrc.2017.109. View

3.
Donzelli S, Fontemaggi G, Fazi F, Di Agostino S, Padula F, Biagioni F . MicroRNA-128-2 targets the transcriptional repressor E2F5 enhancing mutant p53 gain of function. Cell Death Differ. 2011; 19(6):1038-48. PMC: 3354056. DOI: 10.1038/cdd.2011.190. View

4.
Fuertes-Alvarez S, Maeso-Alonso L, Villoch-Fernandez J, Wildung M, Martin-Lopez M, Marshall C . p73 regulates ependymal planar cell polarity by modulating actin and microtubule cytoskeleton. Cell Death Dis. 2018; 9(12):1183. PMC: 6281643. DOI: 10.1038/s41419-018-1205-6. View

5.
Klimovich B, Merle N, Neumann M, Elmshauser S, Nist A, Mernberger M . p53 partial loss-of-function mutations sensitize to chemotherapy. Oncogene. 2021; 41(7):1011-1023. PMC: 8837531. DOI: 10.1038/s41388-021-02141-5. View