生物
肿瘤微环境
谷氨酰胺
胶质瘤
癌变
免疫系统
星形胶质细胞
代谢途径
神经科学
谷氨酸受体
细胞生物学
信号转导
癌症研究
新陈代谢
癌症
中枢神经系统
免疫学
生物化学
受体
遗传学
氨基酸
作者
Jed de Ruiter Swain,Evdokia Michalopoulou,Evan Noch,Michael J. Lukey,Linda Van Aelst
出处
期刊:Genes & Development
[Cold Spring Harbor Laboratory]
日期:2023-08-01
卷期号:37 (15-16): 681-702
被引量:2
标识
DOI:10.1101/gad.350693.123
摘要
The different cell types in the brain have highly specialized roles with unique metabolic requirements. Normal brain function requires the coordinated partitioning of metabolic pathways between these cells, such as in the neuron–astrocyte glutamate–glutamine cycle. An emerging theme in glioblastoma (GBM) biology is that malignant cells integrate into or “hijack” brain metabolism, co-opting neurons and glia for the supply of nutrients and recycling of waste products. Moreover, GBM cells communicate via signaling metabolites in the tumor microenvironment to promote tumor growth and induce immune suppression. Recent findings in this field point toward new therapeutic strategies to target the metabolic exchange processes that fuel tumorigenesis and suppress the anticancer immune response in GBM. Here, we provide an overview of the intercellular division of metabolic labor that occurs in both the normal brain and the GBM tumor microenvironment and then discuss the implications of these interactions for GBM therapy.
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