Molecular Pathways: Dysregulated Glutamatergic Signaling Pathways in Cancer

被引:97
|
作者
Prickett, Todd D. [1 ]
Samuels, Yardena [1 ]
机构
[1] NHGRI, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
PROTEIN-COUPLED RECEPTORS; METASTATIC MELANOMA; NMDA RECEPTORS; GLIOMA-CELLS; IN-VIVO; METABOTROPIC GLUTAMATE-RECEPTOR-1; PHARMACOLOGICAL BLOCKADE; THERAPEUTIC TARGET; HUMAN MELANOCYTES; BRAF INHIBITORS;
D O I
10.1158/1078-0432.CCR-11-1217
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The neurotransmitter glutamate interacts with glutamate receptor proteins, leading to the activation of multiple signaling pathways. Dysfunction in the glutamatergic signaling pathway is well established as a frequent player in diseases such as schizophrenia, Alzheimer disease, and brain tumors (gliomas). Recently, aberrant functioning of this pathway has also been shown in melanoma. In both glioma and melanoma, glutamate secretion stimulates tumor growth, proliferation, and survival through activation of the mitogen-activated protein kinase and phosphoinositide 3-kinase/Akt pathways. In the future, extracellular glutamate levels and glutamatergic signaling may serve as biological markers for tumorigenicity and facilitate targeted therapy for melanoma. Clin Cancer Res; 18(16); 4240-6. (C) 2012 AACR.
引用
收藏
页码:4240 / 4246
页数:7
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