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DNA Damage and Cellular Stress Responses

Glucose Withdrawal Induces Oxidative Stress followed by Apoptosis in Glioblastoma Cells but not in Normal Human Astrocytes

¹ Department of Radiation Oncology and ² Comprehensive Cancer Center, University of California at San Francisco, San Francisco, California

Requests for reprints: Tobias B. Dansen, Department of Physiological Chemistry, University Medical Center Utrecht, Universiteitsweg 100, Room STR 3.233, 3584 CG Utrecht, the Netherlands. Phone: 31-30-2538918; Fax: 31-30-2539035. E-mail: t.b.dansen{at}med.uu.nl

Tumor cells rely preferentially on anaerobic glycolysis rather than on respiration for ATP generation, a phenomenon known as the Warburg effect. We explored the effects of glucose withdrawal on glioblastoma multiforme–derived cell lines and their nontransformed counterparts, normal human astrocytes. We found that glucose withdrawal induces extensive apoptosis in glioblastoma multiforme cells but not in normal astrocytes. In all cells examined, ATP levels are sustained on glucose withdrawal due to elevation of fatty acid oxidation and ensuing respiration; however, we show that oxidative stress generated in the mitochondrial respiratory chain is the direct cause of cell death in glioblastoma multiforme cells. Oxidative stress that only occurs in glioblastoma multiforme cells underlies the selective susceptibility to glucose withdrawal–induced apoptosis documented in the malignant cells. This study implicates glycolysis as a potentially efficient and selective target for glioblastoma multiforme treatment. (Mol Cancer Res 2006;4(5):319–30)

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