Cited by 463Cancer-related Molecular PathwaysMechanisms of cancer metastasisProtease and Inhibitor Mechanisms

p53 and its mutants in tumor cell migration and invasion

Open access
Muller, Patricia A. J., Vousden, Karen H., Norman, Jim C.·2011·Journal of Cell Biology

Abstract

In about half of all human cancers, the tumor suppressor p53 protein is either lost or mutated, frequently resulting in the expression of a transcriptionally inactive mutant p53 protein. Loss of p53 function is well known to influence cell cycle checkpoint controls and apoptosis. But it is now clear that p53 regulates other key stages of metastatic progression, such as cell migration and invasion. Moreover, recent data suggests that expression of mutant p53 is not the equivalent of p53 loss, and that mutant p53s can acquire new functions to drive cell migration, invasion, and metastasis, in part by interfering with p63 function.

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Crossref · 10.1083/jcb.201009059

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  • GOF mut-p53 exhibits interactions with distinct transcription factors (e.g., NF-ɣ, SREBP, VDR, Sp1, ETS2, NFR2, p73, p63) that promote tumor initiation and progression.

    “In contrast to wt-p53, GOF mut-p53 exhibits interactions with distinct transcription factors (e.g., NF-ɣ, SREBP, VDR, Sp1, ETS2, NFR2, p73, p63) that promote tumor initiation and progression [13,72,73,74,75,76,77].”

    From The p53 Pathway in Glioblastoma (2018) · cites this paper as [72]

    The “Mechanisms of mutant p53’s gain of function” section says mutant p53 interacts with the transcription factors p63 and p73 and negatively regulates their function. The Introduction links interference with p63 to tumor-cell migration and metastasis. Our copy does not substantiate the other listed transcription-factor interactions, so it supports only part of the attributed claim; no page numbers are available in the indexed passages. (LLM, conf=0.86)

    Experimental — accuracy not yet measured

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Authors
Muller, P. A. J., Vousden, K. H., & Norman, J. C.
Affiliations
Cancer Research UK Scotland Institute (GB)
Corresponding author
  • Muller, Patricia A. J.
  • Norman, Jim C.
Venue
Journal of Cell Biology
Published
2011-01-24
Volume
192
Issue
2
Pages
209-218
ISSN
  • 0021-9525 (ISSN-L)
  • 1540-8140
OpenAlex
W2005155951
Cited by
463
References
101
Citations by year
2026: 5 · 2025: 15 · 2024: 12 · 2023: 19 · 2022: 24 · 2021: 34 · 2020: 25 · 2019: 28 · 2018: 28 · 2017: 28 · 2016: 39 · 2015: 30 · 2014: 54 · 2013: 55 · 2012: 41
FWCI
5.11
Type
journal article
Language
en
Open access
Licence
cc-by-nc-sa
Locations
  • The Journal of Cell Biology (publishedVersion, cc-by-nc-sa)
  • Europe PMC (PubMed Central) (publishedVersion, cc-by-nc-sa)
  • PubMed Central (publishedVersion, cc-by-nc-sa)
  • PubMed (publishedVersion)
  • ENLIGHTEN (Jurnal Bimbingan dan Konseling Islam) (submittedVersion)
  • Durham Research Online (Durham University) (submittedVersion, cc-by)
Funders
  • Cancer Research UK
  • Nederlandse Organisatie voor Wetenschappelijk Onderzoek
Topics
  • Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mechanisms of cancer metastasis
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Protease and Inhibitor Mechanisms
Keywords
p53, mutant p53, tumor cell migration, tumor invasion, metastasis, p63, tumor suppressor, cell cycle checkpoints, apoptosis
MeSH terms
Animals, Cell Movement, Humans, Neoplasm Invasiveness, Neoplasms, Tumor Suppressor Protein p53, Mutant Proteins

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