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Metabolism and Transcription in Cancer: Merging Two Classic Tales

Cellular plasticity, or the ability of a cancer cell to adapt to changes in the microenvironment, is a major determinant of cell survival and functionality that require the coordination of transcriptional programs with signaling and metabolic pathways. In this scenario, these pathways sense and inte...

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Autores principales: Martín-Martín, Natalia, Carracedo, Arkaitz, Torrano, Verónica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5760552/
https://www.ncbi.nlm.nih.gov/pubmed/29354634
http://dx.doi.org/10.3389/fcell.2017.00119
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author Martín-Martín, Natalia
Carracedo, Arkaitz
Torrano, Verónica
author_facet Martín-Martín, Natalia
Carracedo, Arkaitz
Torrano, Verónica
author_sort Martín-Martín, Natalia
collection PubMed
description Cellular plasticity, or the ability of a cancer cell to adapt to changes in the microenvironment, is a major determinant of cell survival and functionality that require the coordination of transcriptional programs with signaling and metabolic pathways. In this scenario, these pathways sense and integrate nutrient signals for the induction of coordinated gene expression programs in cancer. This minireview focuses on recent advances that shed light on the bidirectional relationship between metabolism and gene transcription, and their biological outcomes in cancer. Specifically, we will discuss how metabolic changes occurring in cancer cells impact on gene expression, both at the level of the epigenetic landscape and transcription factor regulation.
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spelling pubmed-57605522018-01-19 Metabolism and Transcription in Cancer: Merging Two Classic Tales Martín-Martín, Natalia Carracedo, Arkaitz Torrano, Verónica Front Cell Dev Biol Cell and Developmental Biology Cellular plasticity, or the ability of a cancer cell to adapt to changes in the microenvironment, is a major determinant of cell survival and functionality that require the coordination of transcriptional programs with signaling and metabolic pathways. In this scenario, these pathways sense and integrate nutrient signals for the induction of coordinated gene expression programs in cancer. This minireview focuses on recent advances that shed light on the bidirectional relationship between metabolism and gene transcription, and their biological outcomes in cancer. Specifically, we will discuss how metabolic changes occurring in cancer cells impact on gene expression, both at the level of the epigenetic landscape and transcription factor regulation. Frontiers Media S.A. 2018-01-05 /pmc/articles/PMC5760552/ /pubmed/29354634 http://dx.doi.org/10.3389/fcell.2017.00119 Text en Copyright © 2018 Martín-Martín, Carracedo and Torrano. http://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) or licensor 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
Martín-Martín, Natalia
Carracedo, Arkaitz
Torrano, Verónica
Metabolism and Transcription in Cancer: Merging Two Classic Tales
title Metabolism and Transcription in Cancer: Merging Two Classic Tales
title_full Metabolism and Transcription in Cancer: Merging Two Classic Tales
title_fullStr Metabolism and Transcription in Cancer: Merging Two Classic Tales
title_full_unstemmed Metabolism and Transcription in Cancer: Merging Two Classic Tales
title_short Metabolism and Transcription in Cancer: Merging Two Classic Tales
title_sort metabolism and transcription in cancer: merging two classic tales
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5760552/
https://www.ncbi.nlm.nih.gov/pubmed/29354634
http://dx.doi.org/10.3389/fcell.2017.00119
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