TY - JOUR
T1 - The warburg effect suppresses oxidative stress induced apoptosis yeast model for cancer
AU - Ruckenstuhl, Christoph
AU - Büttner, Sabrina
AU - Carmona-Gutierrez, Didac
AU - Eisenberg, Tobias
AU - Kroemer, Guido
AU - Sigrist, Stephan J.
AU - Fröhlich, Kai Uwe
AU - Madeo, Frank
PY - 2009/2/25
Y1 - 2009/2/25
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=84887212425&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0004592
DO - 10.1371/journal.pone.0004592
M3 - Article
AN - SCOPUS:84887212425
SN - 1932-6203
VL - 4
JO - PLoS ONE
JF - PLoS ONE
IS - 2
M1 - e4592
ER -