NUP98-HOXA9 expression in hemopoietic stem cells induces chronic and acute myeloid leukemias in mice

被引:173
作者
Kroon, E
Thorsteinsdottir, U
Mayotte, N
Nakamura, T
Sauvageau, G
机构
[1] Clin Res Inst Montreal, Lab Mol Genet Hemopoiet Stem Cells, Montreal, PQ H2W 1R7, Canada
[2] Univ Montreal, Dept Med, Montreal, PQ H3J 3J7, Canada
[3] Hop Maison Neuve Rosemont, Dept Hematol, Montreal, PQ H1T 2M2, Canada
[4] Japanese Fdn Canc Res, Inst Canc, Dept Carcinogenesis, Tokyo 170, Japan
关键词
AML; Hox; Meis; NUP98; HOXA9; PBX;
D O I
10.1093/emboj/20.3.350
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Here we describe hemopoietic chimeras serving as a mouse model for NUP98-HOXA9-induced leukemia, which reproduced several of the phenotypes observed in human disease. Mice transplanted with bone marrow cells expressing NUP98-HOXA49 through retroviral transduction acquire a myeloproliferative disease (MPD) and eventually succumb to acute myeloid leukemia (AML), The NUP98 portion of the fusion protein was shown to be responsible for transforming a clinically silent pre-leukemic phase observed for Hoxa9 into a chronic, stem cell-derived MPD, The co-expression of NUP98-HOXA9 and Meis1 accelerated the transformation of MPD to AML, identifying a genetic interaction previously observed for Hoxa9 and Meis1, Our findings demonstrate the presence of overlapping yet distinct molecular mechanisms for MPD versus AML, illustrating the complexity of leukemic transformation.
引用
收藏
页码:350 / 361
页数:12
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