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Mutant p53: One, No One, and One Hundred Thousand

Encoded by the mutated variants of the TP53 tumor suppressor gene, mutant p53 proteins are getting an increased experimental support as active oncoproteins promoting tumor growth and metastasis. p53 missense mutant proteins are losing their wild-type tumor suppressor activity and acquire oncogenic p...

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Detalles Bibliográficos
Autores principales: Walerych, Dawid, Lisek, Kamil, Del Sal, Giannino
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4685664/
https://www.ncbi.nlm.nih.gov/pubmed/26734571
http://dx.doi.org/10.3389/fonc.2015.00289
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author Walerych, Dawid
Lisek, Kamil
Del Sal, Giannino
author_facet Walerych, Dawid
Lisek, Kamil
Del Sal, Giannino
author_sort Walerych, Dawid
collection PubMed
description Encoded by the mutated variants of the TP53 tumor suppressor gene, mutant p53 proteins are getting an increased experimental support as active oncoproteins promoting tumor growth and metastasis. p53 missense mutant proteins are losing their wild-type tumor suppressor activity and acquire oncogenic potential, possessing diverse transforming abilities in cell and mouse models. Whether various mutant p53s differ in their oncogenic potential has been a matter of debate. Recent discoveries are starting to uncover the existence of mutant p53 downstream programs that are common to different mutant p53 variants. In this review, we discuss a number of studies on mutant p53, underlining the advantages and disadvantages of alternative experimental approaches that have been used to describe the numerous mutant p53 gain-of-function activities. Therapeutic possibilities are also discussed, taking into account targeting either individual or multiple mutant p53 proteins in human cancer.
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spelling pubmed-46856642016-01-05 Mutant p53: One, No One, and One Hundred Thousand Walerych, Dawid Lisek, Kamil Del Sal, Giannino Front Oncol Oncology Encoded by the mutated variants of the TP53 tumor suppressor gene, mutant p53 proteins are getting an increased experimental support as active oncoproteins promoting tumor growth and metastasis. p53 missense mutant proteins are losing their wild-type tumor suppressor activity and acquire oncogenic potential, possessing diverse transforming abilities in cell and mouse models. Whether various mutant p53s differ in their oncogenic potential has been a matter of debate. Recent discoveries are starting to uncover the existence of mutant p53 downstream programs that are common to different mutant p53 variants. In this review, we discuss a number of studies on mutant p53, underlining the advantages and disadvantages of alternative experimental approaches that have been used to describe the numerous mutant p53 gain-of-function activities. Therapeutic possibilities are also discussed, taking into account targeting either individual or multiple mutant p53 proteins in human cancer. Frontiers Media S.A. 2015-12-21 /pmc/articles/PMC4685664/ /pubmed/26734571 http://dx.doi.org/10.3389/fonc.2015.00289 Text en Copyright © 2015 Walerych, Lisek and Del Sal. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Walerych, Dawid
Lisek, Kamil
Del Sal, Giannino
Mutant p53: One, No One, and One Hundred Thousand
title Mutant p53: One, No One, and One Hundred Thousand
title_full Mutant p53: One, No One, and One Hundred Thousand
title_fullStr Mutant p53: One, No One, and One Hundred Thousand
title_full_unstemmed Mutant p53: One, No One, and One Hundred Thousand
title_short Mutant p53: One, No One, and One Hundred Thousand
title_sort mutant p53: one, no one, and one hundred thousand
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4685664/
https://www.ncbi.nlm.nih.gov/pubmed/26734571
http://dx.doi.org/10.3389/fonc.2015.00289
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