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Author (up) Henkenius, K.; Greene, B.H.; Barckhausen, C.; Hartmann, R.; Marken, M.; Kaiser, T.; Rehberger, M.; Metzelder, S.K.; Parak, W.J.; Neubauer, A.; Brendel, C.; Mack, E. file  url
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  Title Maintenance of cellular respiration indicates drug resistance in acute myeloid leukemia Type Journal Article
  Year 2017 Publication Leukemia Research Abbreviated Journal Leuk Res  
  Volume 62 Issue Pages 56-63  
  Keywords Cell Line, Tumor; Cell Respiration/*physiology; Drug Resistance, Neoplasm/*physiology; Glycolysis/drug effects/physiology; Humans; Leukemia, Myeloid, Acute/*metabolism; Oxidative Phosphorylation/drug effects; Aml; Drug resistance; Mitochondrial membrane potential; Respiration  
  Abstract Primary resistance to induction therapy is an unsolved clinical problem in acute myeloid leukemia (AML). Here we investigated drug resistance in AML at the level of cellular metabolism in order to identify early predictors of therapeutic response. Using extracellular flux analysis, we compared metabolic drug responses in AML cell lines sensitive or resistant to cytarabine or sorafenib after 24h of drug treatment to a small cell lung cancer (SCLC) cell line exposed to etoposide. Only drug-resistant AML cells maintained oxidative metabolism upon drug exposure while SCLC cells displayed an overall metabolic shift towards glycolysis, i.e. a Warburg effect to escape drug toxicity. Moreover, primary AML blasts displayed very low glycolytic activity, while oxygen consumption was readily detectable, indicating an essential role of oxidative pathways in the bioenergetics of AML blasts. In line with these observations, analysis of the mitochondrial membrane potential using tetramethylrhodamine ethyl ester staining and flow cytometry allowed for clear discrimination between drug sensitive and resistant AML cell line clones and primary blasts after 24h of treatment with cytarabine or sorafenib. Our data reveal a distinct metabolic phenotype of resistant AML cells and suggest that disrupting oxidative metabolism rather than glycolysis may enhance the cytotoxic effects of chemotherapy in AML.  
  Call Number Serial 2125  
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