| Literature DB >> 33082514 |
Lyudmila Krassikova1, Boxi Zhang1, Divya Nagarajan1, André Lima Queiroz1,2, Merve Kacal1, Evangelos Samakidis1, Helin Vakifahmetoglu-Norberg1, Erik Norberg3.
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.Entities:
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Year: 2020 PMID: 33082514 PMCID: PMC7937685 DOI: 10.1038/s41418-020-00639-1
Source DB: PubMed Journal: Cell Death Differ ISSN: 1350-9047 Impact factor: 15.828