Mitochondrial
NADPH-dependent
isocitrate dehydrogenase, IDH2, and cytosolic IDH1, catalyze reductive carboxylation of
2-oxoglutarate. Both idh2 and idh1 monoallelic mutations are harbored in grade 2/3
gliomas, secondary
glioblastomas and
acute myeloid leukemia. Mutant IDH1/IDH2
enzymes were reported to form an oncometabolite r-2-hydroxyglutarate (2HG), further strengthening
malignancy. We quantified CO2-dependent reductive carboxylation glutaminolysis (RCG) and CO2-independent 2HG production in HTB-126 and MDA-MB-231
breast carcinoma cells by measuring (13)C incorporation from 1-(13)C-glutamine into
citrate,
malate, and 2HG. For HTB-126 cells, (13)C-citrate, (13)C-malate, and (13)C-2-hydroxyglutarate were enriched by 2-, 5-, and 15-fold at 5mM
glucose (2-, 2.5-, and 13-fold at 25 mM
glucose), respectively, after 6 h. Such enrichment decreased by 6% with IDH1 silencing, but by 30-50% upon IDH2 silencing while cell respiration and
ATP levels rose up to 150%. Unlike 2HG production RCG declined at decreasing CO2. At
hypoxia (5% O2), IDH2-related and unrelated (13)C-accumulation into
citrate and
malate increased 1.5-2.5-fold with unchanged IDH2 expression; whereas hypoxic 2HG formation did not. (13)C-2HG originated by ∼50% from other than IDH2 or IDH1 reactions, substantiating remaining activity in IDH1&2-silenced cells. Relatively high basal (12)C-2HG levels existed (5-fold higher vs. non-
tumor HTB-125 cells) and (13)C-2HG was formed despite the absence of any idh2 and idh1 mutations in HTB-126 cells. Since RCG is enhanced at
hypoxia (frequent in solid
tumors) and 2HG can be formed without idh1/2 mutations, we suggest 2HG as an analytic marker (in serum, urine, or biopsies) predicting
malignancy of
breast cancer in all patients.