Isocitrate Dehydrogenase 2 Dysfunction Contributes to 5-hydroxymethylcytosine Depletion in Gastric Cancer Cells

Anticancer Res. 2016 Aug;36(8):3983-90.

Abstract

The isocitrate dehydrogenase (IDH) family of enzymes comprises of the key functional metabolic enzymes in the Krebs cycle that catalyze the conversion of isocitrate to α-ketoglutarate (α-KG). α-KG acts as a cofactor in the conversion of 5-methylcytosine (5mC) to 5-hydroxymethylcytosine (5hmC). However, the relationship between 5hmC and IDH in gastric cancer remains unclear. Our study revealed that the 5hmC level was substantially lower and 5mC level was slightly higher in gastric cancer tissues; however, 5-formylcytosine (5fC) and 5-carboxylcytosine (5caC) levels did not change significantly in these tissues. We further examined the expression levels of IDH1 and IDH2 in gastric cancer tissues and observed that IDH2 levels were significantly lower in gastric cancer tissues than in the adjacent normal tissues. The ectopic expression of IDH2 can increase 5hmC levels in gastric cancer cells. In conclusion, our results suggested that IDH2 dysfunction is involved in 5hmC depletion during gastric cancer progression.

Keywords: DNA methylation; demethylation; gastric cancer; hydroxymethylation.

MeSH terms

  • 5-Methylcytosine / metabolism
  • Cytosine / analogs & derivatives
  • Cytosine / isolation & purification
  • Cytosine / metabolism
  • DNA Methylation / genetics*
  • Female
  • Humans
  • Isocitrate Dehydrogenase / biosynthesis*
  • Isocitrate Dehydrogenase / genetics
  • Ketoglutaric Acids / metabolism
  • Male
  • Stomach Neoplasms / genetics*
  • Stomach Neoplasms / pathology

Substances

  • 5-carboxylcytosine
  • 5-formylcytosine
  • Ketoglutaric Acids
  • 5-hydroxymethylcytosine
  • 5-Methylcytosine
  • Cytosine
  • IDH2 protein, human
  • Isocitrate Dehydrogenase
  • IDH1 protein, human