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Deshpande, A.J.
;
Cusan, M.
;
Rawat, V.P.S.
;
Reuter, H.
;
Krause, A.
; Pott, C.* ;
Quintanilla-Martinez, L.
;
Kakadia, P.
;
Kuchenbauer, F.
;
Ahmed, F.
; Delabesse, E.* ; Hahn, M.* ; Lichtner, P.* ;
Kneba, M.
;
Hiddemann, W.
; Macintyre, E.* ; Mecucci, C.* ; Ludwig, W.D.* ; Humphries, R.K.* ;
Bohlander, S.K.
;
Feuring-Buske, M.
;
Buske, C.
Acute myeloid leukemia is propagated by a leukemic stem cell with lymphoid characteristics in a mouse model of CALM/AF10-positive leukemia.
Cancer Cell
10
, 363-374 (2006)
DOI
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as soon as Postprint is submitted to ZB.
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A challenge for the development of therapies selectively targeting leukemic stem cells in acute myeloid leukemia (AML) is their similarity to normal hematopoietic stem cells (HSCs). Here we demonstrate that the leukemia-propagating cell in murine CALM/AF10-positive AML differs from normal HSCs by B220 surface expression and immunoglobulin heavy chain rearrangement. Furthermore, depletion of B220+ cells in leukemic transplants impaired development of leukemia in recipients. As in the murine model, human CALM/AF10-positive AML was characterized by CD45RA (B220)-positive, IG DH-JH rearranged leukemic cells. These data demonstrate in a murine leukemia model that AML can be propagated by a transformed progenitor with lymphoid characteristics, which can be targeted by antibodies that do not crossreact with normal HSCs. © 2006 Elsevier Inc. All rights reserved.
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Article: Journal article
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Scientific Article
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Humdisease
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ISSN (print) / ISBN
1535-6108
e-ISSN
1878-3686
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Cancer Cell
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Volume: 10,
Issue: 5,
Pages: 363-374
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Cell Press
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Cambridge, Mass.
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CCG Pathogenesis of Acute Myeloid Leukemia (KKG-KPL)
Institute of Pathology (PATH)
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