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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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Formato: | Texto |
Lenguaje: | English |
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Impact Journals LLC
2010
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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. |
format | Text |
id | pubmed-3018840 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT ericksonjonw glutaminaseahotspotforregulationofcancercellmetabolism AT cerionericharda glutaminaseahotspotforregulationofcancercellmetabolism |