The oncometabolite 2-hydroxyglutarate inhibits histone lysine demethylases.

نویسندگان

  • Rasheduzzaman Chowdhury
  • Kar Kheng Yeoh
  • Ya-Min Tian
  • Lars Hillringhaus
  • Eleanor A Bagg
  • Nathan R Rose
  • Ivanhoe K H Leung
  • Xuan S Li
  • Esther C Y Woon
  • Ming Yang
  • Michael A McDonough
  • Oliver N King
  • Ian J Clifton
  • Robert J Klose
  • Timothy D W Claridge
  • Peter J Ratcliffe
  • Christopher J Schofield
  • Akane Kawamura
چکیده

Mutations in isocitrate dehydrogenases (IDHs) have a gain-of-function effect leading to R(-)-2-hydroxyglutarate (R-2HG) accumulation. By using biochemical, structural and cellular assays, we show that either or both R- and S-2HG inhibit 2-oxoglutarate (2OG)-dependent oxygenases with varying potencies. Half-maximal inhibitory concentration (IC(50)) values for the R-form of 2HG varied from approximately 25 μM for the histone N(ɛ)-lysine demethylase JMJD2A to more than 5 mM for the hypoxia-inducible factor (HIF) prolyl hydroxylase. The results indicate that candidate oncogenic pathways in IDH-associated malignancy should include those that are regulated by other 2OG oxygenases than HIF hydroxylases, in particular those involving the regulation of histone methylation.

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عنوان ژورنال:
  • EMBO reports

دوره 12 5  شماره 

صفحات  -

تاریخ انتشار 2011