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The Warburg Effect Suppresses Oxidative Stress Induced Apoptosis in a Yeast Model for Cancer
BACKGROUND: Otto Warburg observed that cancer cells are often characterized by intense glycolysis in the presence of oxygen and a concomitant decrease in mitochondrial respiration. Research has mainly focused on a possible connection between increased glycolysis and tumor development whereas decreas...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2643009/ https://www.ncbi.nlm.nih.gov/pubmed/19240798 http://dx.doi.org/10.1371/journal.pone.0004592 |
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author | Ruckenstuhl, Christoph Büttner, Sabrina Carmona-Gutierrez, Didac Eisenberg, Tobias Kroemer, Guido Sigrist, Stephan J. Fröhlich, Kai-Uwe Madeo, Frank |
author_facet | Ruckenstuhl, Christoph Büttner, Sabrina Carmona-Gutierrez, Didac Eisenberg, Tobias Kroemer, Guido Sigrist, Stephan J. Fröhlich, Kai-Uwe Madeo, Frank |
author_sort | Ruckenstuhl, Christoph |
collection | PubMed |
description | BACKGROUND: Otto Warburg observed that cancer cells are often characterized by intense glycolysis in the presence of oxygen and a concomitant decrease in mitochondrial respiration. Research has mainly focused on a possible connection between increased glycolysis and tumor development whereas decreased respiration has largely been left unattended. Therefore, a causal relation between decreased respiration and tumorigenesis has not been demonstrated. METHODOLOGY/PRINCIPAL FINDINGS: For this purpose, colonies of Saccharomyces cerevisiae, which is suitable for manipulation of mitochondrial respiration and shows mitochondria-mediated cell death, were used as a model. Repression of respiration as well as ROS-scavenging via glutathione inhibited apoptosis and conferred a survival advantage during seeding and early development of this fast proliferating solid cell population. In contrast, enhancement of respiration triggered cell death. CONCLUSION/SIGNIFICANCE: Thus, the Warburg effect might directly contribute to the initiation of cancer formation - not only by enhanced glycolysis - but also via decreased respiration in the presence of oxygen, which suppresses apoptosis. |
format | Text |
id | pubmed-2643009 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-26430092009-02-25 The Warburg Effect Suppresses Oxidative Stress Induced Apoptosis in a Yeast Model for Cancer Ruckenstuhl, Christoph Büttner, Sabrina Carmona-Gutierrez, Didac Eisenberg, Tobias Kroemer, Guido Sigrist, Stephan J. Fröhlich, Kai-Uwe Madeo, Frank PLoS One Research Article BACKGROUND: Otto Warburg observed that cancer cells are often characterized by intense glycolysis in the presence of oxygen and a concomitant decrease in mitochondrial respiration. Research has mainly focused on a possible connection between increased glycolysis and tumor development whereas decreased respiration has largely been left unattended. Therefore, a causal relation between decreased respiration and tumorigenesis has not been demonstrated. METHODOLOGY/PRINCIPAL FINDINGS: For this purpose, colonies of Saccharomyces cerevisiae, which is suitable for manipulation of mitochondrial respiration and shows mitochondria-mediated cell death, were used as a model. Repression of respiration as well as ROS-scavenging via glutathione inhibited apoptosis and conferred a survival advantage during seeding and early development of this fast proliferating solid cell population. In contrast, enhancement of respiration triggered cell death. CONCLUSION/SIGNIFICANCE: Thus, the Warburg effect might directly contribute to the initiation of cancer formation - not only by enhanced glycolysis - but also via decreased respiration in the presence of oxygen, which suppresses apoptosis. Public Library of Science 2009-02-25 /pmc/articles/PMC2643009/ /pubmed/19240798 http://dx.doi.org/10.1371/journal.pone.0004592 Text en Ruckenstuhl et al. http://creativecommons.org/licenses/by/4.0/ 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 properly credited. |
spellingShingle | Research Article Ruckenstuhl, Christoph Büttner, Sabrina Carmona-Gutierrez, Didac Eisenberg, Tobias Kroemer, Guido Sigrist, Stephan J. Fröhlich, Kai-Uwe Madeo, Frank The Warburg Effect Suppresses Oxidative Stress Induced Apoptosis in a Yeast Model for Cancer |
title | The Warburg Effect Suppresses Oxidative Stress Induced Apoptosis in a Yeast Model for Cancer |
title_full | The Warburg Effect Suppresses Oxidative Stress Induced Apoptosis in a Yeast Model for Cancer |
title_fullStr | The Warburg Effect Suppresses Oxidative Stress Induced Apoptosis in a Yeast Model for Cancer |
title_full_unstemmed | The Warburg Effect Suppresses Oxidative Stress Induced Apoptosis in a Yeast Model for Cancer |
title_short | The Warburg Effect Suppresses Oxidative Stress Induced Apoptosis in a Yeast Model for Cancer |
title_sort | warburg effect suppresses oxidative stress induced apoptosis in a yeast model for cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2643009/ https://www.ncbi.nlm.nih.gov/pubmed/19240798 http://dx.doi.org/10.1371/journal.pone.0004592 |
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