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Endothelial cell metabolism and implications for cancer therapy

Tumour tissue is characterised by fluctuating oxygen concentrations, decreased nutrient supply, and acidic pH. The primarily glycolytic metabolism of tumour cells contributes to this, with increased glucose consumption and increased lactate secretion. Endothelial cells are particularly challenged wh...

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Detalles Bibliográficos
Autores principales: Harjes, U, Bensaad, K, Harris, A L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3494441/
https://www.ncbi.nlm.nih.gov/pubmed/23047591
http://dx.doi.org/10.1038/bjc.2012.398
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author Harjes, U
Bensaad, K
Harris, A L
author_facet Harjes, U
Bensaad, K
Harris, A L
author_sort Harjes, U
collection PubMed
description Tumour tissue is characterised by fluctuating oxygen concentrations, decreased nutrient supply, and acidic pH. The primarily glycolytic metabolism of tumour cells contributes to this, with increased glucose consumption and increased lactate secretion. Endothelial cells are particularly challenged when recruited towards the tumour metabolic environment. They are required to proliferate and form functional networks in order to establish continuous blood flow. Considering that deregulated metabolism is an emerging hallmark of cancer and target of tumour therapy, it is of importance to incorporate the current knowledge about how the tumour metabolic environment, as a therapy target, can affect endothelial cell metabolism and the angiogenic response. Recent studies have shown differences in metabolic pathways in endothelial cells compared with other normal or tumour tissues. Therefore, we have reviewed relevant literature on endothelial metabolism and the response to angiogenic activation in conditions of metabolic stress.
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spelling pubmed-34944412012-11-09 Endothelial cell metabolism and implications for cancer therapy Harjes, U Bensaad, K Harris, A L Br J Cancer Minireview Tumour tissue is characterised by fluctuating oxygen concentrations, decreased nutrient supply, and acidic pH. The primarily glycolytic metabolism of tumour cells contributes to this, with increased glucose consumption and increased lactate secretion. Endothelial cells are particularly challenged when recruited towards the tumour metabolic environment. They are required to proliferate and form functional networks in order to establish continuous blood flow. Considering that deregulated metabolism is an emerging hallmark of cancer and target of tumour therapy, it is of importance to incorporate the current knowledge about how the tumour metabolic environment, as a therapy target, can affect endothelial cell metabolism and the angiogenic response. Recent studies have shown differences in metabolic pathways in endothelial cells compared with other normal or tumour tissues. Therefore, we have reviewed relevant literature on endothelial metabolism and the response to angiogenic activation in conditions of metabolic stress. Nature Publishing Group 2012-10-09 2012-10-09 /pmc/articles/PMC3494441/ /pubmed/23047591 http://dx.doi.org/10.1038/bjc.2012.398 Text en Copyright © 2012 Cancer Research UK https://creativecommons.org/licenses/by-nc-sa/3.0/This work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Minireview
Harjes, U
Bensaad, K
Harris, A L
Endothelial cell metabolism and implications for cancer therapy
title Endothelial cell metabolism and implications for cancer therapy
title_full Endothelial cell metabolism and implications for cancer therapy
title_fullStr Endothelial cell metabolism and implications for cancer therapy
title_full_unstemmed Endothelial cell metabolism and implications for cancer therapy
title_short Endothelial cell metabolism and implications for cancer therapy
title_sort endothelial cell metabolism and implications for cancer therapy
topic Minireview
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3494441/
https://www.ncbi.nlm.nih.gov/pubmed/23047591
http://dx.doi.org/10.1038/bjc.2012.398
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