Buczkowska Joanna, Szeliga Monika
Department of Neurotoxicology, Mossakowski Medical Research Institute, Polish Academy of Sciences, 5 Pawińskiego Str., 02-106 Warsaw, Poland.
Cancers (Basel). 2023 Nov 24;15(23):5566. doi: 10.3390/cancers15235566.
In rapidly proliferating cancer cells, glutamine is a major source of energy and building blocks. Increased glutamine uptake and enhanced glutaminolysis are key metabolic features of many cancers. Glutamine is metabolized by glutaminase (GA), which is encoded by two genes: and . In contrast to isoforms arising from the gene, which clearly act as oncoproteins, the role of products in tumorigenesis is far from well understood. While in some cancer types is overexpressed and drives cancer development, in some other types it is downregulated and behaves as a tumor suppressor gene. In this review, we describe the essential functions and regulatory mechanisms of human GLS2 and the cellular compartments in which GLS2 has been localized. Furthermore, we present the context-dependent oncogenic and tumor-suppressor properties of GLS2, and delve into the mechanisms underlying these phenomena.
在快速增殖的癌细胞中,谷氨酰胺是能量和构建模块的主要来源。谷氨酰胺摄取增加和谷氨酰胺分解增强是许多癌症的关键代谢特征。谷氨酰胺由谷氨酰胺酶(GA)代谢,谷氨酰胺酶由两个基因编码: 和 。与 基因产生的同工型明显作为癌蛋白不同, 产物在肿瘤发生中的作用远未得到充分理解。虽然在某些癌症类型中 过表达并驱动癌症发展,但在其他一些类型中它被下调并表现为肿瘤抑制基因。在本综述中,我们描述了人类GLS2的基本功能和调节机制以及GLS2所在的细胞区室。此外,我们介绍了GLS2依赖于背景的致癌和肿瘤抑制特性,并深入探讨了这些现象背后的机制。