| Literature DB >> 30506321 |
Keisuke Miyake1, Yoshifumi Baba1, Takatsugu Ishimoto1, Yukiharu Hiyoshi1, Masaaki Iwatsuki1, Yuji Miyamoto1, Naoya Yoshida1, Masayuki Watanabe2, Yoko Ogata1, Megumi Nagayama3, Atit Silsirivanit3,4, Daiki Kobayashi3, Norie Araki3, Hideo Baba5.
Abstract
Isocitrate dehydrogenase 1 and 2 (IDH1 and IDH2) are key metabolic enzymes that convert isocitrate to α-ketoglutarate. Somatic point mutations in IDH1/2 confer a gain-of-function in cancer cells, resulting in overproduction of an oncometabolite, 2-hydroxyglutarate (2HG). 2HG interferes with cellular metabolism and epigenetic regulation, contributing to oncogenesis. Given that IDH1 and IDH2 are attracting attention as promising therapeutic targets, better evaluation of the incidence of IDH1 and IDH2 mutations and 2HG level in human cancers is clinically important. This is the first study to assess their incidence in esophageal squamous cell carcinomas (ESCCs). First, we established pyrosequencing assays for IDH1 and IDH2 mutations and revealed that these mutations were absent in 10 ESCC cell lines and 96 ESCC tissues. Second, utilizing IDH1 and IDH2 overexpression vectors, we demonstrated that LC-MS/MS assays can accurately evaluate 2HG level and found that some ESCC cases presented a high level of 2HG. In conclusion, IDH1 or IDH2 mutations play a limited role in the development of ESCC. 2HG is potentially synthesized to high levels in the absence of IDH1 and IDH2 mutations, and this may correlate with progression of ESCCs.Entities:
Keywords: 2-Hydroxyglutarate; Esophageal squamous cell carcinoma; Isocitrate dehydrogenase; Oncometabolite; α-Ketoglutaric acid
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Year: 2018 PMID: 30506321 DOI: 10.1007/s12032-018-1229-x
Source DB: PubMed Journal: Med Oncol ISSN: 1357-0560 Impact factor: 3.738