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• W2078692783 endingPage "e51426" @default.
• W2078692783 startingPage "e51426" @default.
• W2078692783 abstract "Numerous p53 missense mutations possess gain-of-function activities. Studies in mouse models have demonstrated that the stabilization of p53 R172H (R175H in human) mutant protein, by currently unknown factors, is a prerequisite for its oncogenic gain-of-function phenotype such as tumour progression and metastasis. Here we show that MDM2-dependent ubiquitination and degradation of p53 R175H mutant protein in mouse embryonic fibroblasts is partially inhibited by increasing concentration of heat shock protein 70 (HSP70/HSPA1-A). These phenomena correlate well with the appearance of HSP70-dependent folding intermediates in the form of dynamic cytoplasmic spots containing aggregate-prone p53 R175H and several molecular chaperones. We propose that a transient but recurrent interaction with HSP70 may lead to an increase in mutant p53 protein half-life. In the presence of MDM2 these pseudoaggregates can form stable amyloid-like structures, which occasionally merge into an aggresome. Interestingly, formation of folding intermediates is not observed in the presence of HSC70/HSPA8, the dominant-negative K71S variant of HSP70 or HSP70 inhibitor. In cancer cells, where endogenous HSP70 levels are already elevated, mutant p53 protein forms nuclear aggregates without the addition of exogenous HSP70. Aggregates containing p53 are also visible under conditions where p53 is partially unfolded: 37°C for temperature-sensitive variant p53 V143A and 42°C for wild-type p53. Refolding kinetics of p53 indicate that HSP70 causes transient exposure of p53 aggregate-prone domain(s). We propose that formation of HSP70- and MDM2-dependent protein coaggregates in tumours with high levels of these two proteins could be one of the mechanisms by which mutant p53 is stabilized. Moreover, sequestration of p73 tumour suppressor protein by these nuclear aggregates may lead to gain-of-function phenotypes." @default.
• W2078692783 created "2016-06-24" @default.
• W2078692783 creator A5032209489 @default.
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• W2078692783 creator A5073515303 @default.
• W2078692783 creator A5077590296 @default.
• W2078692783 creator A5078713898 @default.
• W2078692783 date "2012-12-12" @default.
• W2078692783 modified "2023-10-16" @default.
• W2078692783 title "Molecular Mechanism of Mutant p53 Stabilization: The Role of HSP70 and MDM2" @default.
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• W2078692783 doi "https://doi.org/10.1371/journal.pone.0051426" @default.
• W2078692783 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3520893" @default.
• W2078692783 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/23251530" @default.
• W2078692783 hasPublicationYear "2012" @default.

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