Replication Study: The common feature of leukemia-associated IDH1 and IDH2 mutations is a neomorphic enzyme activity converting alpha-ketoglutarate to 2-hydroxyglutarate

Elife. 2017 Jun 27:6:e26030. doi: 10.7554/eLife.26030.

Abstract

In 2016, as part of the Reproducibility Project: Cancer Biology, we published a Registered Report (Fiehn et al., 2016), that described how we intended to replicate selected experiments from the paper "The common feature of leukemia-associated IDH1 and IDH2 mutations is a neomorphic enzyme activity converting alpha-ketoglutarate to 2-hydroxyglutarate" (Ward et al., 2010). Here, we report the results of those experiments. We found that cells expressing R172K mutant IDH2 did not display isocitrate-dependent NADPH production above vector control levels, in contrast to the increased production observed with wild-type IDH2. Conversely, expression of R172K mutant IDH2 resulted in increased alpha-ketoglutarate-dependent consumption of NADPH compared to wild-type IDH2 or vector control. These results are similar to those reported in the original study (Figure 2; Ward et al., 2010). Further, expression of R172K mutant IDH2 resulted in increased 2HG levels within cells compared to the background levels observed in wild-type IDH2 and vector control, similar to the original study (Figure 3D; Ward et al., 2010). In primary human AML samples, the 2HG levels observed in samples with mutant IDH1 or IDH2 status were higher than those observed in samples without an IDH mutation, similar to what was observed in the original study (Figure 5C; Ward et al., 2010). Finally, we report meta-analyses for each result.

Keywords: 2-HG; Reproducibility Project: Cancer Biology; acute myeloid leukemia; biochemistry; cancer biology; human; metascience; replication; reproducibility.

MeSH terms

  • Biotransformation
  • Glutarates
  • Humans
  • Isocitrate Dehydrogenase / genetics
  • Isocitrate Dehydrogenase / metabolism*
  • Ketoglutaric Acids / metabolism*
  • Leukemia, Myeloid, Acute / pathology*
  • Mutant Proteins / genetics
  • Mutant Proteins / metabolism*
  • NADP / metabolism
  • Tumor Cells, Cultured

Substances

  • Glutarates
  • Ketoglutaric Acids
  • Mutant Proteins
  • alpha-hydroxyglutarate
  • NADP
  • IDH2 protein, human
  • Isocitrate Dehydrogenase
  • IDH1 protein, human

Grants and funding

The funder had no role in study design, data collection and interpretation, or the decision to submit the work for publication.