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