The t(6;9) associated DEK/CAN fusion protein targets a population of long-term repopulating hematopoietic stem cells for leukemogenic transformation

Leukemia. 2010 Nov;24(11):1910-9. doi: 10.1038/leu.2010.180. Epub 2010 Sep 9.

Abstract

The t(6;9)-positive acute myeloid leukemia (AML) is classified as a separate clinical entity because of its early onset and poor prognosis. The hallmark of t(6;9) AML is the expression of the DEK/CAN fusion protein. The leukemogenic potential of DEK/CAN has been called into question, because it was shown to be unable to block the differentiation of hematopoietic progenitors. We found that DEK/CAN initiated leukemia from a small subpopulation within the hematopoietic stem cell (HSC) population expressing a surface marker pattern of long-term (LT) HSC. The propagation of established DEK/CAN-positive leukemia was not restricted to the LT-HSC population, but occurred even from more mature and heterogeneous cell populations. This finding indicates that in DEK/CAN-induced leukemia, there is a difference between 'leukemia-initiating cells' (L-ICs) and 'leukemia-maintaining cells' (L-MCs). In contrast to the L-IC cells represented by a very rare subpopulation of LT-HSC, the L-MC seem to be represented by a larger and phenotypically heterogeneous cell population.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Ly / genetics
  • Cell Differentiation
  • Colony-Forming Units Assay
  • DNA-Binding Proteins / genetics*
  • Female
  • Hematopoietic Stem Cells / cytology*
  • Hematopoietic Stem Cells / drug effects
  • Hematopoietic Stem Cells / physiology
  • Leukemia, Experimental / genetics
  • Leukemia, Myeloid, Acute / genetics*
  • Leukemia, Myeloid, Acute / pathology
  • Membrane Proteins / genetics
  • Mice
  • Mice, Inbred C57BL
  • Mutagenesis, Site-Directed
  • Nuclear Pore Complex Proteins / genetics
  • Oncogene Proteins / genetics*
  • Open Reading Frames
  • Poly-ADP-Ribose Binding Proteins
  • Recombinant Fusion Proteins / pharmacology
  • Splenomegaly / pathology
  • Translocation, Genetic

Substances

  • Antigens, Ly
  • DEK protein, mouse
  • DNA-Binding Proteins
  • Ly6a protein, mouse
  • Membrane Proteins
  • Nuclear Pore Complex Proteins
  • Oncogene Proteins
  • Poly-ADP-Ribose Binding Proteins
  • Recombinant Fusion Proteins