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Glutaminase: A Hot Spot For Regulation Of Cancer Cell Metabolism?

Cancer cells re-program their metabolic machinery in order to satisfy their bioenergetic and biosynthetic requirements. A critical aspect of the re-programming of cancer cell metabolism involves changes in the glycolytic pathway (referred to as the “Warburg effect”). As an outcome of these changes,...

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Autores principales: Erickson, Jon W., Cerione, Richard A.
Formato: Texto
Lenguaje:English
Publicado: Impact Journals LLC 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3018840/
https://www.ncbi.nlm.nih.gov/pubmed/21234284
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author Erickson, Jon W.
Cerione, Richard A.
author_facet Erickson, Jon W.
Cerione, Richard A.
author_sort Erickson, Jon W.
collection PubMed
description Cancer cells re-program their metabolic machinery in order to satisfy their bioenergetic and biosynthetic requirements. A critical aspect of the re-programming of cancer cell metabolism involves changes in the glycolytic pathway (referred to as the “Warburg effect”). As an outcome of these changes, much of the pyruvate generated via the glycolytic pathway is converted to lactic acid, rather than being used to produce acetyl-CoA and ultimately, the citrate which enters the citric acid cycle. In order to compensate for these changes and to help maintain a functioning citric acid cycle, cancer cells often rely on elevated glutamine metabolism. Recently, we have found that this is achieved through a marked elevation of glutaminase activity in cancer cells. Here we further consider these findings and the possible mechanisms by which this important metabolic activity is regulated.
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spelling pubmed-30188402011-01-11 Glutaminase: A Hot Spot For Regulation Of Cancer Cell Metabolism? Erickson, Jon W. Cerione, Richard A. Oncotarget Research Perspectives Cancer cells re-program their metabolic machinery in order to satisfy their bioenergetic and biosynthetic requirements. A critical aspect of the re-programming of cancer cell metabolism involves changes in the glycolytic pathway (referred to as the “Warburg effect”). As an outcome of these changes, much of the pyruvate generated via the glycolytic pathway is converted to lactic acid, rather than being used to produce acetyl-CoA and ultimately, the citrate which enters the citric acid cycle. In order to compensate for these changes and to help maintain a functioning citric acid cycle, cancer cells often rely on elevated glutamine metabolism. Recently, we have found that this is achieved through a marked elevation of glutaminase activity in cancer cells. Here we further consider these findings and the possible mechanisms by which this important metabolic activity is regulated. Impact Journals LLC 2010-12-09 /pmc/articles/PMC3018840/ /pubmed/21234284 Text en Copyright: © 2010 Erickson and Cerione http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
spellingShingle Research Perspectives
Erickson, Jon W.
Cerione, Richard A.
Glutaminase: A Hot Spot For Regulation Of Cancer Cell Metabolism?
title Glutaminase: A Hot Spot For Regulation Of Cancer Cell Metabolism?
title_full Glutaminase: A Hot Spot For Regulation Of Cancer Cell Metabolism?
title_fullStr Glutaminase: A Hot Spot For Regulation Of Cancer Cell Metabolism?
title_full_unstemmed Glutaminase: A Hot Spot For Regulation Of Cancer Cell Metabolism?
title_short Glutaminase: A Hot Spot For Regulation Of Cancer Cell Metabolism?
title_sort glutaminase: a hot spot for regulation of cancer cell metabolism?
topic Research Perspectives
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3018840/
https://www.ncbi.nlm.nih.gov/pubmed/21234284
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