IDH2 mutations in patients with D-2-hydroxyglutaric aciduria

Science. 2010 Oct 15;330(6002):336. doi: 10.1126/science.1192632. Epub 2010 Sep 16.

Abstract

Heterozygous somatic mutations in the genes encoding isocitrate dehydrogenase-1 and -2 (IDH1 and IDH2) were recently discovered in human neoplastic disorders. These mutations disable the enzymes' normal ability to convert isocitrate to 2-ketoglutarate (2-KG) and confer on the enzymes a new function: the ability to convert 2-KG to d-2-hydroxyglutarate (D-2-HG). We have detected heterozygous germline mutations in IDH2 that alter enzyme residue Arg(140) in 15 unrelated patients with d-2-hydroxyglutaric aciduria (D-2-HGA), a rare neurometabolic disorder characterized by supraphysiological levels of D-2-HG. These findings provide additional impetus for investigating the role of D-2-HG in the pathophysiology of metabolic disease and cancer.

MeSH terms

  • Adolescent
  • Brain Diseases, Metabolic, Inborn / genetics*
  • Brain Neoplasms / genetics
  • Brain Neoplasms / metabolism
  • Child
  • Child, Preschool
  • Female
  • Germ-Line Mutation*
  • Glutarates / metabolism*
  • Glutarates / urine
  • Heterozygote
  • Humans
  • Infant
  • Isocitrate Dehydrogenase / chemistry
  • Isocitrate Dehydrogenase / genetics*
  • Isocitrate Dehydrogenase / metabolism
  • Male
  • Neoplasms / genetics
  • Neoplasms / metabolism
  • Young Adult

Substances

  • Glutarates
  • alpha-hydroxyglutarate
  • IDH2 protein, human
  • Isocitrate Dehydrogenase
  • IDH1 protein, human