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Published in: Journal of Neuro-Oncology 1/2008

01-10-2008 | Clinical-Patient Studies

Glucose metabolites, glutamate and glycerol in malignant glioma tumours during radiotherapy

Authors: Pedram Tabatabaei, Per Bergström, Roger Henriksson, A. Tommy Bergenheim

Published in: Journal of Neuro-Oncology | Issue 1/2008

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Abstract

Objective The metabolism of malignant glioma was studied in 13 patients. The main objective was to perform a study of the metabolic pattern of glucose, lactate, pyruvate, glutamate and glycerol in tumour tissue during base-line conditions and to detect any changes in the metabolism during radiotherapy. Method During a stereotactic biopsy, two microdialysis catheters were implanted: one in tumour and one in peri-tumoural tissue. Fasting samples were analysed daily, before and during 5 days of radiotherapy given with 2 Gy fractions. Results Base-line levels of glucose and pyruvate were significantly lower in tumour compared to peri-tumoural tissue (P = 0.04 and 0.023, respectively). The lactate/pyruvate ratio was significantly higher in tumour tissue (P = 0.022). In general, the levels of lactate, glutamate and glycerol were higher in tumour tissue, although not statistically significant. Further, we could not detect any significant changes during the 5 days of radiotherapy in any of the metabolites analysed. Conclusion Radiotherapy up to 10 Gy given in five fractions does not influence the glucose metabolism nor does it induce any acute cytotoxic effect detected with glutamate or glycerol in malignant glioma, as assessed by microdialysis. The study confirms the glycolytic properties of glucose metabolism in malignant glioma.
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Metadata
Title
Glucose metabolites, glutamate and glycerol in malignant glioma tumours during radiotherapy
Authors
Pedram Tabatabaei
Per Bergström
Roger Henriksson
A. Tommy Bergenheim
Publication date
01-10-2008
Publisher
Springer US
Published in
Journal of Neuro-Oncology / Issue 1/2008
Print ISSN: 0167-594X
Electronic ISSN: 1573-7373
DOI
https://doi.org/10.1007/s11060-008-9625-2

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