Adenosine present in human brain glioma extracellular spaces is a marker of astrocyte purine metabolism. In this study, we evaluated adenosine levels in the extracellular fluid of 21 human gliomas of high-grade malignancy using brain microdialysis techniques coupled to high-performance liquid chromatography. The adenosine concentration (mean +/- SEM) within the control tissue was 2.99 +/- 0.37 muM and in the tumour tissue 1.56 +/- 0.46 muM. The reduction was statistically significant. It is concluded that the adenosine concentrations reached in the tumour tissue are sufficient to stimulate all adenosine receptor subtypes, suppress local anti-tumour immune responses and affect glial and endothelial cell proliferation. (C) 2003 Elsevier Science Ireland Ltd. All rights reserved.

Adenosine extracellular levels in human brain gliomas: an intraoperative microdialysis study / Melani A; De Micheli E; Pinna G; Alfieri A; Della Corte L; Pedata F.. - In: NEUROSCIENCE LETTERS. - ISSN 0304-3940. - STAMPA. - 346:(2003), pp. 93-96.

Adenosine extracellular levels in human brain gliomas: an intraoperative microdialysis study.

MELANI, ALESSIA;DELLA CORTE, LAURA;PEDATA, FELICITA
2003

Abstract

Adenosine present in human brain glioma extracellular spaces is a marker of astrocyte purine metabolism. In this study, we evaluated adenosine levels in the extracellular fluid of 21 human gliomas of high-grade malignancy using brain microdialysis techniques coupled to high-performance liquid chromatography. The adenosine concentration (mean +/- SEM) within the control tissue was 2.99 +/- 0.37 muM and in the tumour tissue 1.56 +/- 0.46 muM. The reduction was statistically significant. It is concluded that the adenosine concentrations reached in the tumour tissue are sufficient to stimulate all adenosine receptor subtypes, suppress local anti-tumour immune responses and affect glial and endothelial cell proliferation. (C) 2003 Elsevier Science Ireland Ltd. All rights reserved.
2003
346
93
96
Melani A; De Micheli E; Pinna G; Alfieri A; Della Corte L; Pedata F.
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/311559
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