Abstract
Acute promyelocytic leukemia (APL) is characterized by the accumulation of abnormal promyelocytes in the bone marrow (BM), and by the presence of a reciprocal chromosomal translocation involving retinoic acid receptor alpha (RARα). To date, five RARα partner genes have been identified in APL. NuMA-RARα was identified in a pediatric case of APL carrying a translocation t(11;17)(q13;q21). Using a construct containing the NuMA-RARα fusion gene driven by the human cathepsin G promoter (hCG-NuMA-RARα), two transgenic mouse lines were generated. Transgenic mice were observed to have a genetic myeloproliferation (increased granulopoiesis in BM) at an early age, and rapidly developed a myeloproliferative disease-like myeloid leukemia. This leukemia was morphologically and immunophenotypically indistinguishable from human APL, with a penetrance of 100%. The phenotype of transgenic mice was consistent with a blockade of neutrophil differentiation. NuMA-RARα is therefore sufficient for disease development in this APL model.
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Abbreviations
- APL:
-
acute promyelocytic leukemia
- ATRA:
-
all trans-retinoic acid
- BM:
-
bone marrow
- CFU:
-
colony-forming unit
- LTMC:
-
long-term marrow culture
- My/Ly:
-
myeloid/lymphoid
- MPD:
-
myeloproliferative disorder
- NPM :
-
nucleophosmin
- NuMA :
-
nuclear mitotic apparatus
- PB:
-
peripheral blood
- PML :
-
promyelocytic leukemia
- PLZF :
-
promyelocytic leukemia zinc-finger
- RARα :
-
retinoic acid receptor alpha
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Acknowledgements
We thank Dr S Arora for reading of the manuscript. This work was supported by funding from the National Cancer Institute of Canada (Grant #13087 to SK-R) and the National Institutes of Health (Grant #s R01 CA74031, R01 CA71692, and U01 CA84292 to PPP). MAS is an Ontario Graduate Scholar. We also gratefully acknowledge the disability accommodations funding provided through the University of Toronto, Office of Accessibility Services.
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Sukhai, M., Wu, X., Xuan, Y. et al. Myeloid leukemia with promyelocytic features in transgenic mice expressing hCG-NuMA-RARα. Oncogene 23, 665–678 (2004). https://doi.org/10.1038/sj.onc.1207073
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DOI: https://doi.org/10.1038/sj.onc.1207073