Epilepsy in glioblastoma multiforme: correlation with glutamine synthetase levels
Adult
Male
0301 basic medicine
Epilepsy
Brain Neoplasms
Blotting, Western
Astrocytes; Cerebral glioma; Epilepsy; Epileptogenesis; Glutamine synthetase
Middle Aged
03 medical and health sciences
Glutamate-Ammonia Ligase
Humans
Female
Glioblastoma
Aged
DOI:
10.1007/s11060-008-9794-z
Publication Date:
2009-01-29T16:19:54Z
AUTHORS (11)
ABSTRACT
The hypothesis addressed by this study is that a glutamine synthetase (GS) deficiency in neoplastic astrocytes is a possible molecular basis associated with seizure generation in glioblastoma multiforme (GBM).Quantitative Western blot analysis of GS was performed in 20 individuals operated for malignant glioma.The levels of GS in patients with GBM and epilepsy were significantly lower (range 0.04-1.15; mean 0.35 +/- 0.36; median 0.25) than in non-epileptic GBM individuals (range 0.78-3.97; mean 1.64 +/- 0.99; median 1.25; P = 0.002). No relationship has been found between histological features (i.e. necrosis, gliosis, stroma, inflammatory cells, giant cells, and haemosiderine) and GS expression or epilepsy.Even though the epileptogenesis in glioma is multifactorial, it is conceivable that a down-regulation of GS may have an important pro-epileptogenic role in GBM, through the slowing of glutamate-glutamine cycle. This study suggests that seizures in GBM are coupled with a highly localized enzyme deficiency. The manipulation of GS activity might constitute a novel principle for inhibiting seizures in patients with glioma epilepsy.
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