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Control of Nucleotide Metabolism Enables Mutant p53’s Oncogenic Gain-of-Function Activity
Since its discovery as an oncoprotein in 1979, investigation into p53’s many identities has completed a full circle and today it is inarguably the most extensively studied tumor suppressor (wild-type p53 form or WTp53) and oncogene (mutant p53 form or mtp53) in cancer research. After the p53 protein...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5751358/ https://www.ncbi.nlm.nih.gov/pubmed/29257071 http://dx.doi.org/10.3390/ijms18122759 |
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author | Schmidt, Valentina Nagar, Rachana Martinez, Luis A. |
author_facet | Schmidt, Valentina Nagar, Rachana Martinez, Luis A. |
author_sort | Schmidt, Valentina |
collection | PubMed |
description | Since its discovery as an oncoprotein in 1979, investigation into p53’s many identities has completed a full circle and today it is inarguably the most extensively studied tumor suppressor (wild-type p53 form or WTp53) and oncogene (mutant p53 form or mtp53) in cancer research. After the p53 protein was declared “Molecule of the Year” by Science in 1993, the p53 field exploded and a plethora of excellent reviews is now available on every aspect of p53 genetics and functional repertoire in a cell. Nevertheless, new functions of p53 continue to emerge. Here, we discuss a novel mechanism that contributes to mtp53’s Gain of Functions GOF (gain-of-function) activities and involves the upregulation of both nucleotide de novo synthesis and nucleoside salvage pathways. |
format | Online Article Text |
id | pubmed-5751358 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-57513582018-01-08 Control of Nucleotide Metabolism Enables Mutant p53’s Oncogenic Gain-of-Function Activity Schmidt, Valentina Nagar, Rachana Martinez, Luis A. Int J Mol Sci Review Since its discovery as an oncoprotein in 1979, investigation into p53’s many identities has completed a full circle and today it is inarguably the most extensively studied tumor suppressor (wild-type p53 form or WTp53) and oncogene (mutant p53 form or mtp53) in cancer research. After the p53 protein was declared “Molecule of the Year” by Science in 1993, the p53 field exploded and a plethora of excellent reviews is now available on every aspect of p53 genetics and functional repertoire in a cell. Nevertheless, new functions of p53 continue to emerge. Here, we discuss a novel mechanism that contributes to mtp53’s Gain of Functions GOF (gain-of-function) activities and involves the upregulation of both nucleotide de novo synthesis and nucleoside salvage pathways. MDPI 2017-12-19 /pmc/articles/PMC5751358/ /pubmed/29257071 http://dx.doi.org/10.3390/ijms18122759 Text en © 2017 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 (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Schmidt, Valentina Nagar, Rachana Martinez, Luis A. Control of Nucleotide Metabolism Enables Mutant p53’s Oncogenic Gain-of-Function Activity |
title | Control of Nucleotide Metabolism Enables Mutant p53’s Oncogenic Gain-of-Function Activity |
title_full | Control of Nucleotide Metabolism Enables Mutant p53’s Oncogenic Gain-of-Function Activity |
title_fullStr | Control of Nucleotide Metabolism Enables Mutant p53’s Oncogenic Gain-of-Function Activity |
title_full_unstemmed | Control of Nucleotide Metabolism Enables Mutant p53’s Oncogenic Gain-of-Function Activity |
title_short | Control of Nucleotide Metabolism Enables Mutant p53’s Oncogenic Gain-of-Function Activity |
title_sort | control of nucleotide metabolism enables mutant p53’s oncogenic gain-of-function activity |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5751358/ https://www.ncbi.nlm.nih.gov/pubmed/29257071 http://dx.doi.org/10.3390/ijms18122759 |
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