Abstract
Using a mouse model of human acute myeloid leukemia (AML) induced by the MLL-AF9 oncogene, we demonstrate that colony-forming cells (CFCs) in the bone marrow and spleen of leukemic mice are also leukemia stem cells (LSCs). These self-renewing cells (1) are frequent, accounting for 25%-30% of myeloid lineage cells at late-stage disease; (2) generate a phenotypic, morphologic, and functional leukemia cell hierarchy; (3) express mature myeloid lineage-specific antigens; and (4) exhibit altered microenvironmental interactions by comparison with the oncogene-immortalized CFCs that initiated the disease. Therefore, the LSCs responsible for sustaining, expanding, and regenerating MLL-AF9 AML are downstream myeloid lineage cells, which have acquired an aberrant Hox-associated self-renewal program as well as other biologic features of hematopoietic stem cells. © 2006 Elsevier Inc. All rights reserved.
Original language | English |
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Pages (from-to) | 257-268 |
Number of pages | 11 |
Journal | Cancer Cell |
Volume | 10 |
Issue number | 4 |
DOIs | |
Publication status | Published - Oct 2006 |
Keywords
- CELLCYCLE
- STEMCELL
Research Beacons, Institutes and Platforms
- Manchester Cancer Research Centre