Selective inhibition of Ezh2 by a small molecule inhibitor blocks tumor cells proliferation.

نویسندگان

  • Wei Qi
  • HoMan Chan
  • Lin Teng
  • Ling Li
  • Shannon Chuai
  • Ruipeng Zhang
  • Jue Zeng
  • Min Li
  • Hong Fan
  • Ying Lin
  • Justin Gu
  • Ophelia Ardayfio
  • Ji-Hu Zhang
  • Xiaoxia Yan
  • Jialuo Fang
  • Yuan Mi
  • Man Zhang
  • Tao Zhou
  • Grace Feng
  • Zijun Chen
  • Guobin Li
  • Teddy Yang
  • Kehao Zhao
  • Xianghui Liu
  • Zhengtian Yu
  • Chris X Lu
  • Peter Atadja
  • En Li
چکیده

Ezh2 (Enhancer of zeste homolog 2) protein is the enzymatic component of the Polycomb repressive complex 2 (PRC2), which represses gene expression by methylating lysine 27 of histone H3 (H3K27) and regulates cell proliferation and differentiation during embryonic development. Recently, hot-spot mutations of Ezh2 were identified in diffused large B-cell lymphomas and follicular lymphomas. To investigate if tumor growth is dependent on the enzymatic activity of Ezh2, we developed a potent and selective small molecule inhibitor, EI1, which inhibits the enzymatic activity of Ezh2 through direct binding to the enzyme and competing with the methyl group donor S-Adenosyl methionine. EI1-treated cells exhibit genome-wide loss of H3K27 methylation and activation of PRC2 target genes. Furthermore, inhibition of Ezh2 by EI1 in diffused large B-cell lymphomas cells carrying the Y641 mutations results in decreased proliferation, cell cycle arrest, and apoptosis. These results provide strong validation of Ezh2 as a potential therapeutic target for the treatment of cancer.

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عنوان ژورنال:
  • Proceedings of the National Academy of Sciences of the United States of America

دوره 109 52  شماره 

صفحات  -

تاریخ انتشار 2012