Identification of the KDM2/7 Histone Lysine Demethylase Subfamily Inhibitor and its Antiproliferative Activity

نویسندگان

  • Takayoshi Suzuki
  • Hiroki Ozasa
  • Yukihiro Itoh
  • Peng Zhan
  • Hideyuki Sawada
  • Koshiki Mino
  • Louise Walport
  • Rei Ohkubo
  • Akane Kawamura
  • Masato Yonezawa
  • Yuichi Tsukada
  • Anthony Tumber
  • Hidehiko Nakagawa
  • Makoto Hasegawa
  • Ryuzo Sasaki
  • Tamio Mizukami
  • Christopher J. Schofield
  • Naoki Miyata
چکیده

Histone N(ε)-methyl lysine demethylases KDM2/7 have been identified as potential targets for cancer therapies. On the basis of the crystal structure of KDM7B, we designed and prepared a series of hydroxamate analogues bearing an alkyl chain. Enzyme assays revealed that compound 9 potently inhibits KDM2A, KDM7A, and KDM7B, with IC50s of 6.8, 0.2, and 1.2 μM, respectively. While inhibitors of KDM4s did not show any effect on cancer cells tested, the KDM2/7-subfamily inhibitor 9 exerted antiproliferative activity, indicating the potential for KDM2/7 inhibitors as anticancer agents.

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عنوان ژورنال:

دوره 56  شماره 

صفحات  -

تاریخ انتشار 2013