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去泛素化酶 JOSD2 是葡萄糖代谢的正向调节因子。

The deubiquitinase JOSD2 is a positive regulator of glucose metabolism.

机构信息

Department of Physiology and Pharmacology, Biomedicum, Karolinska Institutet, Solnavägen 9, SE-171 65, Stockholm, Sweden.

Department of Medicine, Weill Cornell Medicine, New York, NY, 10065, USA.

出版信息

Cell Death Differ. 2021 Mar;28(3):1091-1109. doi: 10.1038/s41418-020-00639-1. Epub 2020 Oct 20.

Abstract

Cancer cells undergo complex metabolic alterations. The mechanisms underlying the tuning of cancer metabolism are under active investigation. Here, we identify the uncharacterized deubiquitinase JOSD2 as a positive regulator of cancer cell proliferation by displaying comprehensive effects on glucose catabolism. We found that JOSD2 directly controls a metabolic enzyme complex that includes Aldolase A, Phosphofructokinase-1 and Phosphoglycerate dehydrogenase, in vitro and in vivo. Further, JOSD2 expression, but not a catalytically inactive mutant, deubiquitinates and stabilizes the enzyme complex, thereby enhancing their activities and the glycolytic rate. This represents a selective JOSD2 feature that is not shared among other Machado-Joseph disease DUBs or observed in nontransformed cells. JOSD2 deficiency displays cytostatic effects and reduces glycolysis in a broad spectrum of tumor cells of distinct origin and its expression correlates with poor prognosis in non-small cell lung cancer. Overall, our study provides evidence for a previously unknown biological mechanism in which JOSD2 integrates glucose and serine metabolism with potential therapeutic implications.

摘要

癌细胞经历复杂的代谢改变。癌症代谢调节的机制正在积极研究中。在这里,我们通过显示对葡萄糖分解代谢的全面影响,将未被描述的去泛素酶 JOSD2 鉴定为癌细胞增殖的正调节剂。我们发现 JOSD2 直接控制包括醛缩酶 A、磷酸果糖激酶-1 和磷酸甘油酸脱氢酶在内的代谢酶复合物,在体外和体内都是如此。此外,JOSD2 表达,而不是催化失活的突变体,去泛素化并稳定酶复合物,从而增强它们的活性和糖酵解速率。这代表了 JOSD2 的一个选择性特征,在其他 Machado-Joseph 病 DUB 中没有共享,也没有在非转化细胞中观察到。JOSD2 缺乏显示出细胞停滞效应,并降低广泛来源的不同肿瘤细胞中的糖酵解作用,其表达与非小细胞肺癌的预后不良相关。总的来说,我们的研究提供了一个以前未知的生物学机制的证据,其中 JOSD2 将葡萄糖和丝氨酸代谢与潜在的治疗意义整合在一起。

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