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Drugging in the absence of p53

Inactivation of the p53 gene is a key driver of tumorigenesis in various cancer cohorts and types. The quest for a successful p53-based therapy that holds the promise of treating more than half of the cancer population has culminated in extensive knowledge about the role and function of p53 and led...

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Detalles Bibliográficos
Autores principales: Aning, Obed Akwasi, Cheok, Chit Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6478123/
https://www.ncbi.nlm.nih.gov/pubmed/30865230
http://dx.doi.org/10.1093/jmcb/mjz012
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author Aning, Obed Akwasi
Cheok, Chit Fang
author_facet Aning, Obed Akwasi
Cheok, Chit Fang
author_sort Aning, Obed Akwasi
collection PubMed
description Inactivation of the p53 gene is a key driver of tumorigenesis in various cancer cohorts and types. The quest for a successful p53-based therapy that holds the promise of treating more than half of the cancer population has culminated in extensive knowledge about the role and function of p53 and led to new proposed innovative strategies against p53-defective cancers. We will discuss some of these latest studies with a focus on metabolic regulation and DNA damage response and also highlight novel functions of p53 in these pathways that may provide a contemporary rationale for targeting p53 loss in tumors.
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spelling pubmed-64781232019-04-25 Drugging in the absence of p53 Aning, Obed Akwasi Cheok, Chit Fang J Mol Cell Biol Invited Review Inactivation of the p53 gene is a key driver of tumorigenesis in various cancer cohorts and types. The quest for a successful p53-based therapy that holds the promise of treating more than half of the cancer population has culminated in extensive knowledge about the role and function of p53 and led to new proposed innovative strategies against p53-defective cancers. We will discuss some of these latest studies with a focus on metabolic regulation and DNA damage response and also highlight novel functions of p53 in these pathways that may provide a contemporary rationale for targeting p53 loss in tumors. Oxford University Press 2019-03-28 /pmc/articles/PMC6478123/ /pubmed/30865230 http://dx.doi.org/10.1093/jmcb/mjz012 Text en © The Author(s) (2019). Published by Oxford University Press on behalf of Journal of Molecular Cell Biology, IBCB, SIBS, CAS. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Invited Review
Aning, Obed Akwasi
Cheok, Chit Fang
Drugging in the absence of p53
title Drugging in the absence of p53
title_full Drugging in the absence of p53
title_fullStr Drugging in the absence of p53
title_full_unstemmed Drugging in the absence of p53
title_short Drugging in the absence of p53
title_sort drugging in the absence of p53
topic Invited Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6478123/
https://www.ncbi.nlm.nih.gov/pubmed/30865230
http://dx.doi.org/10.1093/jmcb/mjz012
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