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Regulation of Metabolic Activity by p53

Metabolic reprogramming in cancer cells is controlled by the activation of multiple oncogenic signalling pathways in order to promote macromolecule biosynthesis during rapid proliferation. Cancer cells also need to adapt their metabolism to survive and multiply under the metabolically compromised co...

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Detalles Bibliográficos
Autores principales: Flöter, Jessica, Kaymak, Irem, Schulze, Almut
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487992/
https://www.ncbi.nlm.nih.gov/pubmed/28531108
http://dx.doi.org/10.3390/metabo7020021
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author Flöter, Jessica
Kaymak, Irem
Schulze, Almut
author_facet Flöter, Jessica
Kaymak, Irem
Schulze, Almut
author_sort Flöter, Jessica
collection PubMed
description Metabolic reprogramming in cancer cells is controlled by the activation of multiple oncogenic signalling pathways in order to promote macromolecule biosynthesis during rapid proliferation. Cancer cells also need to adapt their metabolism to survive and multiply under the metabolically compromised conditions provided by the tumour microenvironment. The tumour suppressor p53 interacts with the metabolic network at multiple nodes, mostly to reduce anabolic metabolism and promote preservation of cellular energy under conditions of nutrient restriction. Inactivation of this tumour suppressor by deletion or mutation is a frequent event in human cancer. While loss of p53 function lifts an important barrier to cancer development by deleting cell cycle and apoptosis checkpoints, it also removes a crucial regulatory mechanism and can render cancer cells highly sensitive to metabolic perturbation. In this review, we will summarise the major concepts of metabolic regulation by p53 and explore how this knowledge can be used to selectively target p53 deficient cancer cells in the context of the tumour microenvironment.
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spelling pubmed-54879922017-06-30 Regulation of Metabolic Activity by p53 Flöter, Jessica Kaymak, Irem Schulze, Almut Metabolites Review Metabolic reprogramming in cancer cells is controlled by the activation of multiple oncogenic signalling pathways in order to promote macromolecule biosynthesis during rapid proliferation. Cancer cells also need to adapt their metabolism to survive and multiply under the metabolically compromised conditions provided by the tumour microenvironment. The tumour suppressor p53 interacts with the metabolic network at multiple nodes, mostly to reduce anabolic metabolism and promote preservation of cellular energy under conditions of nutrient restriction. Inactivation of this tumour suppressor by deletion or mutation is a frequent event in human cancer. While loss of p53 function lifts an important barrier to cancer development by deleting cell cycle and apoptosis checkpoints, it also removes a crucial regulatory mechanism and can render cancer cells highly sensitive to metabolic perturbation. In this review, we will summarise the major concepts of metabolic regulation by p53 and explore how this knowledge can be used to selectively target p53 deficient cancer cells in the context of the tumour microenvironment. MDPI 2017-05-20 /pmc/articles/PMC5487992/ /pubmed/28531108 http://dx.doi.org/10.3390/metabo7020021 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
Flöter, Jessica
Kaymak, Irem
Schulze, Almut
Regulation of Metabolic Activity by p53
title Regulation of Metabolic Activity by p53
title_full Regulation of Metabolic Activity by p53
title_fullStr Regulation of Metabolic Activity by p53
title_full_unstemmed Regulation of Metabolic Activity by p53
title_short Regulation of Metabolic Activity by p53
title_sort regulation of metabolic activity by p53
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487992/
https://www.ncbi.nlm.nih.gov/pubmed/28531108
http://dx.doi.org/10.3390/metabo7020021
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