G PROTEIN-COUPLED RECEPTORS AS ONCOGENIC SIGNALS IN GLIOMA: EMERGING THERAPEUTIC AVENUES

被引:36
作者
Cherry, A. E. [1 ]
Stella, N. [1 ,2 ]
机构
[1] Univ Washington, Dept Pharmacol, Seattle, WA 98195 USA
[2] Univ Washington, Dept Psychiat & Behav Sci, Seattle, WA 98195 USA
关键词
glioblastoma multiforme; astrocytoma; G protein-coupled receptor; receptor tyrosine kinase; EPIDERMAL-GROWTH-FACTOR; INDUCED CELL-PROLIFERATION; PHASE-II TRIAL; ACUTE MYELOID-LEUKEMIA; NF-KAPPA-B; SUBSTANCE-P; LYSOPHOSPHATIDIC ACID; SPHINGOSINE; 1-PHOSPHATE; GLIOBLASTOMA-MULTIFORME; FORMYLPEPTIDE RECEPTOR;
D O I
10.1016/j.neuroscience.2014.08.015
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Gliomas are the most common malignant intracranial tumors. Newly developed targeted therapies for these cancers aim to inhibit oncogenic signals, many of which emanate from receptor tyrosine kinases, including the epidermal growth factor receptor (EGFR) and the vascular endothelial growth factor receptor (VEGFR). Unfortunately, the first-generation treatments targeting these oncogenic signals provide little survival benefit in both mouse xenograft models and human patients. The search for new treatment options has uncovered several G protein- coupled receptor (GPCR) candidates and generated a growing interest in this class of proteins as alternative therapeutic targets for the treatment of various cancers, including glioblastoma multiforme (GBM). GPCRs constitute a large family of membrane receptors that influence oncogenic pathways through canonical and non-canonical signaling. Accordingly, evidence indicates that GPCRs display a unique ability to crosstalk with receptor tyrosine kinases, making them important molecular components controlling tumorigenesis. This review summarizes the current research on GPCR functionality in gliomas and explores the potential of modulating these receptors to treat this devastating disease. (C) 2014 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:222 / 236
页数:15
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