Mohan Aditya A, Tomaszewski William H, Haskell-Mendoza Aden P, Hotchkiss Kelly M, Singh Kirit, Reedy Jessica L, Fecci Peter E, Sampson John H, Khasraw Mustafa
Preston Robert Tisch Brain Tumor Center at Duke, Department of Neurosurgery, Duke University Medical Center, Durham, NC, United States.
Front Oncol. 2021 Jun 16;11:696402. doi: 10.3389/fonc.2021.696402. eCollection 2021.
We have only recently begun to understand how cancer metabolism affects antitumor responses and immunotherapy outcomes. Certain immunometabolic targets have been actively pursued in other tumor types, however, glioblastoma research has been slow to exploit the therapeutic vulnerabilities of immunometabolism. In this review, we highlight the pathways that are most relevant to glioblastoma and focus on how these immunometabolic pathways influence tumor growth and immune suppression. We discuss hypoxia, glycolysis, tryptophan metabolism, arginine metabolism, 2-Hydroxyglutarate (2HG) metabolism, adenosine metabolism, and altered phospholipid metabolism, in order to provide an analysis and overview of the field of glioblastoma immunometabolism.
直到最近,我们才开始了解癌症代谢如何影响抗肿瘤反应和免疫治疗结果。某些免疫代谢靶点在其他肿瘤类型中已得到积极研究,然而,胶质母细胞瘤研究在利用免疫代谢的治疗弱点方面进展缓慢。在本综述中,我们重点介绍了与胶质母细胞瘤最相关的途径,并关注这些免疫代谢途径如何影响肿瘤生长和免疫抑制。我们讨论了缺氧、糖酵解、色氨酸代谢、精氨酸代谢、2-羟基戊二酸(2HG)代谢、腺苷代谢以及改变的磷脂代谢,以便对胶质母细胞瘤免疫代谢领域进行分析和概述。