Targeting apoptosis pathways in glioblastoma

被引:60
|
作者
Eisele, Guenter [1 ]
Weller, Michael [1 ]
机构
[1] Univ Zurich Hosp, Dept Neurol, CH-8091 Zurich, Switzerland
关键词
Glioblastoma; Apoptosis; Targeted therapy; HUMAN GLIOMA-CELLS; PHASE-II TRIAL; TRAIL-INDUCED APOPTOSIS; HUMAN-MALIGNANT GLIOMA; FAMILY PROTEIN EXPRESSION; HIGH-GRADE ASTROCYTOMAS; FAS LIGAND EXPRESSION; SURVIVIN EXPRESSION; DEATH RECEPTOR; SYNERGISTIC CYTOTOXICITY;
D O I
10.1016/j.canlet.2010.12.012
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The treatment of glioblastoma remains a major challenge for clinicians since these highly aggressive brain tumors are relatively resistant towards radio- and chemotherapy. The pathways that control apoptosis are altered in glioblastoma cells leading to resistance towards apoptotic stimuli in general. In this review we describe the alterations affecting the p53 pathway, the BCL-2 protein family, the inhibitor of apoptosis proteins and several growth factor pathways involved in the regulation of programmed cell death and define possible targets for new therapies within these apoptotic pathways in glioblastomas. Moreover, we review strategies to target death receptor pathways, most notably to render the glioblastoma cells more susceptible towards this approach without enhancing toxicity in general. Most of the strategies targeting apoptosis in glioblastomas presented here are in a pre-clinical stage of development, however, they all share the ultimative goal to improve the outcome for glioblastoma patients. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:335 / 345
页数:11
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