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p63 and p53: Collaborative Partners or Dueling Rivals?

The tumor suppressor p53 and its oncogenic sibling p63 (ΔNp63) direct opposing fates in tumor development. These paralog proteins are transcription factors that elicit their tumor suppressive and oncogenic capacity through the regulation of both shared and unique target genes. Both proteins predomin...

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Detalles Bibliográficos
Autores principales: Woodstock, Dana L., Sammons, Morgan A., Fischer, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8287303/
https://www.ncbi.nlm.nih.gov/pubmed/34291055
http://dx.doi.org/10.3389/fcell.2021.701986
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author Woodstock, Dana L.
Sammons, Morgan A.
Fischer, Martin
author_facet Woodstock, Dana L.
Sammons, Morgan A.
Fischer, Martin
author_sort Woodstock, Dana L.
collection PubMed
description The tumor suppressor p53 and its oncogenic sibling p63 (ΔNp63) direct opposing fates in tumor development. These paralog proteins are transcription factors that elicit their tumor suppressive and oncogenic capacity through the regulation of both shared and unique target genes. Both proteins predominantly function as activators of transcription, leading to a paradigm shift away from ΔNp63 as a dominant negative to p53 activity. The discovery of p53 and p63 as pioneer transcription factors regulating chromatin structure revealed new insights into how these paralogs can both positively and negatively influence each other to direct cell fate. The previous view of a strict rivalry between the siblings needs to be revisited, as p53 and p63 can also work together toward a common goal.
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spelling pubmed-82873032021-07-20 p63 and p53: Collaborative Partners or Dueling Rivals? Woodstock, Dana L. Sammons, Morgan A. Fischer, Martin Front Cell Dev Biol Cell and Developmental Biology The tumor suppressor p53 and its oncogenic sibling p63 (ΔNp63) direct opposing fates in tumor development. These paralog proteins are transcription factors that elicit their tumor suppressive and oncogenic capacity through the regulation of both shared and unique target genes. Both proteins predominantly function as activators of transcription, leading to a paradigm shift away from ΔNp63 as a dominant negative to p53 activity. The discovery of p53 and p63 as pioneer transcription factors regulating chromatin structure revealed new insights into how these paralogs can both positively and negatively influence each other to direct cell fate. The previous view of a strict rivalry between the siblings needs to be revisited, as p53 and p63 can also work together toward a common goal. Frontiers Media S.A. 2021-07-05 /pmc/articles/PMC8287303/ /pubmed/34291055 http://dx.doi.org/10.3389/fcell.2021.701986 Text en Copyright © 2021 Woodstock, Sammons and Fischer. https://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) and the copyright owner(s) 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 Cell and Developmental Biology
Woodstock, Dana L.
Sammons, Morgan A.
Fischer, Martin
p63 and p53: Collaborative Partners or Dueling Rivals?
title p63 and p53: Collaborative Partners or Dueling Rivals?
title_full p63 and p53: Collaborative Partners or Dueling Rivals?
title_fullStr p63 and p53: Collaborative Partners or Dueling Rivals?
title_full_unstemmed p63 and p53: Collaborative Partners or Dueling Rivals?
title_short p63 and p53: Collaborative Partners or Dueling Rivals?
title_sort p63 and p53: collaborative partners or dueling rivals?
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8287303/
https://www.ncbi.nlm.nih.gov/pubmed/34291055
http://dx.doi.org/10.3389/fcell.2021.701986
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