• Title of article

    The Histone Demethylase KDM1A Sustains the Oncogenic Potential of MLL-AF9 Leukemia Stem Cells

  • Author/Authors

    Harris، نويسنده , , William J. and Huang، نويسنده , , Xu and Lynch، نويسنده , , James T. and Spencer، نويسنده , , Gary J. and Hitchin، نويسنده , , James R. and Li، نويسنده , , Yaoyong and Ciceri، نويسنده , , Filippo and Blaser، نويسنده , , Julian G. and Greystoke، نويسنده , , Brigit F. and Jordan، نويسنده , , Allan M. and Miller، نويسنده , , Crispin J. and Ogilvie، نويسنده , , Donald J. and Somervaille، نويسنده , , Tim C.P.، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2012
  • Pages
    15
  • From page
    473
  • To page
    487
  • Abstract
    Summary a mouse model of human MLL-AF9 leukemia, we identified the lysine-specific demethylase KDM1A (LSD1 or AOF2) as an essential regulator of leukemia stem cell (LSC) potential. KDM1A acts at genomic loci bound by MLL-AF9 to sustain expression of the associated oncogenic program, thus preventing differentiation and apoptosis. In vitro and in vivo pharmacologic targeting of KDM1A using tranylcypromine analogs active in the nanomolar range phenocopied Kdm1a knockdown in both murine and primary human AML cells exhibiting MLL translocations. By contrast, the clonogenic and repopulating potential of normal hematopoietic stem and progenitor cells was spared. Our data establish KDM1A as a key effector of the differentiation block in MLL leukemia, which may be selectively targeted to therapeutic effect.
  • Journal title
    Cancer Cell
  • Serial Year
    2012
  • Journal title
    Cancer Cell
  • Record number

    1337857