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Role of p53 in Cell Death and Human Cancers

p53 is a nuclear transcription factor with a pro-apoptotic function. Since over 50% of human cancers carry loss of function mutations in p53 gene, p53 has been considered to be one of the classical type tumor suppressors. Mutant p53 acts as the dominant-negative inhibitor toward wild-type p53. Indee...

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Detalles Bibliográficos
Autores principales: Ozaki, Toshinori, Nakagawara, Akira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3756401/
https://www.ncbi.nlm.nih.gov/pubmed/24212651
http://dx.doi.org/10.3390/cancers3010994
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author Ozaki, Toshinori
Nakagawara, Akira
author_facet Ozaki, Toshinori
Nakagawara, Akira
author_sort Ozaki, Toshinori
collection PubMed
description p53 is a nuclear transcription factor with a pro-apoptotic function. Since over 50% of human cancers carry loss of function mutations in p53 gene, p53 has been considered to be one of the classical type tumor suppressors. Mutant p53 acts as the dominant-negative inhibitor toward wild-type p53. Indeed, mutant p53 has an oncogenic potential. In some cases, malignant cancer cells bearing p53 mutations display a chemo-resistant phenotype. In response to a variety of cellular stresses such as DNA damage, p53 is induced to accumulate in cell nucleus to exert its pro-apoptotic function. Activated p53 promotes cell cycle arrest to allow DNA repair and/or apoptosis to prevent the propagation of cells with serious DNA damage through the transactivation of its target genes implicated in the induction of cell cycle arrest and/or apoptosis. Thus, the DNA-binding activity of p53 is tightly linked to its tumor suppressive function. In the present review article, we describe the regulatory mechanisms of p53 and also p53-mediated therapeutic strategies to cure malignant cancers.
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spelling pubmed-37564012013-09-04 Role of p53 in Cell Death and Human Cancers Ozaki, Toshinori Nakagawara, Akira Cancers (Basel) Review p53 is a nuclear transcription factor with a pro-apoptotic function. Since over 50% of human cancers carry loss of function mutations in p53 gene, p53 has been considered to be one of the classical type tumor suppressors. Mutant p53 acts as the dominant-negative inhibitor toward wild-type p53. Indeed, mutant p53 has an oncogenic potential. In some cases, malignant cancer cells bearing p53 mutations display a chemo-resistant phenotype. In response to a variety of cellular stresses such as DNA damage, p53 is induced to accumulate in cell nucleus to exert its pro-apoptotic function. Activated p53 promotes cell cycle arrest to allow DNA repair and/or apoptosis to prevent the propagation of cells with serious DNA damage through the transactivation of its target genes implicated in the induction of cell cycle arrest and/or apoptosis. Thus, the DNA-binding activity of p53 is tightly linked to its tumor suppressive function. In the present review article, we describe the regulatory mechanisms of p53 and also p53-mediated therapeutic strategies to cure malignant cancers. Molecular Diversity Preservation International (MDPI) 2011-03-03 /pmc/articles/PMC3756401/ /pubmed/24212651 http://dx.doi.org/10.3390/cancers3010994 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Ozaki, Toshinori
Nakagawara, Akira
Role of p53 in Cell Death and Human Cancers
title Role of p53 in Cell Death and Human Cancers
title_full Role of p53 in Cell Death and Human Cancers
title_fullStr Role of p53 in Cell Death and Human Cancers
title_full_unstemmed Role of p53 in Cell Death and Human Cancers
title_short Role of p53 in Cell Death and Human Cancers
title_sort role of p53 in cell death and human cancers
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3756401/
https://www.ncbi.nlm.nih.gov/pubmed/24212651
http://dx.doi.org/10.3390/cancers3010994
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