Lactonization of the Oncometabolite D-2-Hydroxyglutarate Produces a Novel Endogenous Metabolite
Authors:
- Raffaela S. BergerRBRaffaela S. Berger
- Christian J. WachsmuthCWChristian J. Wachsmuth
- Magdalena C. WaldhierMWMagdalena C. Waldhier
- Kathrin Renner-SattlerKRKathrin Renner-Sattler
- Simone ThomasSTSimone Thomas
- Anuhar ChaturvediACAnuhar Chaturvedi
- Hans-Helmut NillerHNHans-Helmut Niller
- Elisabeth BumesEBElisabeth Bumes
- Peter HauPeter Hau
- Martin ProescholdtMPMartin Proescholdt
- Wolfram GronwaldWolfram Gronwald
- Michael HeuserMHMichael Heuser
Open Access
Abstract
In recent years, onco-metabolites like D-2-hydroxyglutarate, which is produced in isocitrate dehydrogenase-mutated tumors, have gained increasing interest. Here, we report a metabolite in human specimens that is closely related to 2-hydroxyglutarate: the intramolecular ester of 2-hydroxyglutarate, 2-hydroxyglutarate-γ-lactone. Using 13C5-L-glutamine tracer analysis, we showed that 2-hydroxyglutarate is the endogenous precursor of 2-hydroxyglutarate-lactone and that there is a high exchange between these two metabolites. Lactone formation does not depend on mutated isocitrate dehydrogenase, but its formation is most probably linked to transport processes across the cell membrane and favored at low environmental pH. Furthermore, human macrophages showed not only striking differences in uptake of 2-hydroxyglutarate and its lactone but also in the enantiospecific hydrolysis of the latter. Consequently, 2-hydroxyglutarate-lactone may play a critical role in the modulation of the tumor microenvironment.Keywords
Funding Information
- Deutsche Forschungsgemeinschaft (DFG KFO262)
- European Regional Development Fund (Interreg V BY-CZ118)
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