A novel treatment strategy for glioblastoma multiforme and glioma associated seizures: Increasing glutamate uptake with PPARγ agonists

被引:9
作者
Ching, Jared [1 ,3 ,4 ]
Amiridis, Stephanie [1 ,3 ]
Stylli, Stanley S. [1 ,2 ]
Morokofff, Andrew P. [1 ,2 ]
O'Brien, Terence J. [3 ]
Kaye, Andrew H. [1 ,2 ]
机构
[1] Univ Melbourne, Royal Melbourne Hosp, Dept Surg, Melbourne, Vic 3010, Australia
[2] Royal Melbourne Hosp, Dept Neurosurg, Parkville, Vic 3050, Australia
[3] Univ Melbourne, Royal Melbourne Hosp, Dept Med, Melbourne, Vic 3010, Australia
[4] Univ Aberdeen, Inst Med Sci, Aberdeen AB25 2ZD, Scotland
关键词
Glioma; Glutamate; PPAR gamma; Seizures; PROLIFERATOR-ACTIVATED RECEPTORS; GLYCOGEN-SYNTHASE KINASE-3-BETA; PENTYLENETETRAZOLE-INDUCED SEIZURES; OXYGEN-GLUCOSE DEPRIVATION; AMINO-ACID TRANSPORTER-2; CELL-DEATH; MOLECULAR PATHOLOGY; PROLONGED SURVIVAL; CRYSTAL-STRUCTURE; HORMONE-RECEPTOR;
D O I
10.1016/j.jocn.2014.09.001
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The established role of glutamate in the pathogenesis of glioma-associated seizures (GAS) led us to investigate a novel treatment method using an established drug class, peroxisome proliferator activated receptor (PPAR) gamma agonists. Previously, sulfasalazine has been shown to prevent release of glutamate from glioma cells and prevent GAS in rodent models. However, raising protein mediated glutamate transport via excitatory amino acid transporter 2 (EAAT2) has not been investigated previously to our knowledge. PPAR gamma agonists are known to upregulate functional EAAT2 expression in astrocytes and prevent excitotoxicity caused by glutamate excess. These agents are also known to have antineoplastic mechanisms. Herein we discuss and review the potential mechanisms of these drugs and highlight a novel potential treatment for GAS. Crown Copyright (C) 2014 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:21 / 28
页数:8
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