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Cited by 1,247

The DOI matches its Crossref record; 30 of the 30 references it cites were found in a registry or an index.

Mutant p53: one name, many proteins

Open access
Freed-Pastor, William A., Prives, Carol·2012·Genes & Development

Abstract

There is now strong evidence that mutation not only abrogates p53 tumor-suppressive functions, but in some instances can also endow mutant proteins with novel activities. Such neomorphic p53 proteins are capable of dramatically altering tumor cell behavior, primarily through their interactions with other cellular proteins and regulation of cancer cell transcriptional programs. Different missense mutations in p53 may confer unique activities and thereby offer insight into the mutagenic events that drive tumor progression. Here we review mechanisms by which mutant p53 exerts its cellular effects, with a particular focus on the burgeoning mutant p53 transcriptome, and discuss the biological and clinical consequences of mutant p53 gain of function.

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Metadata

Authors
Freed-Pastor, W. A., & Prives, C.
Venue
Genes & Development
Published
2012-06-15
Volume
26
Issue
12
Pages
1268-1286
ISSN
  • 0890-9369 (ISSN-L)
  • 1549-5477
OpenAlex
W2069452349
Cited by
1,247
References
30
Type
posted content
Language
en
Open access
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CoChat. (2026). Citation check: Mutant p53: one name, many proteins. https://app.cochat.ai/papers/10.1101/gad.190678.112
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Freed-Pastor, W. A., & Prives, C. (2012). Mutant p53: one name, many proteins. Genes & Development. https://doi.org/10.1101/gad.190678.112

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.