赖氨酸琥珀酰化和SIRT5将营养状况与谷氨酰胺分解代谢联系起来。

Molecular & cellular oncology Pub Date : 2020-03-19 eCollection Date: 2020-01-01 DOI:10.1080/23723556.2020.1735284
Michael J Lukey, Kai Su Greene, Richard A Cerione
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引用次数: 7

摘要

肿瘤代谢微环境的特点是波动和有限的营养可利用性。为了在这些条件下生存,癌细胞的内在机制感知并发出营养状态的信号。我们描述了谷氨酰胺酶(GLS)如何通过赖氨酸琥珀酰化而不稳定,并通过NAD+依赖的去琥珀酰化酶sirtuin 5 (SIRT5)稳定,将营养水平与代谢通量耦合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lysine succinylation and SIRT5 couple nutritional status to glutamine catabolism.

The metabolic microenvironment of tumors is characterized by fluctuating and limited nutrient availability. To survive these conditions, cancer cell-intrinsic mechanisms sense and signal nutritional status. We describe how glutaminase (GLS) is destabilized by lysine succinylation and stabilized by the NAD+-dependent desuccinylase sirtuin 5 (SIRT5), coupling nutrient levels to metabolic flux.

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