Journal article
c-Myc rapidly induces acute myeloid leukemia in mice without evidence of lymphoma-associated antiapoptotic mutations
Blood, Vol.106(7), pp.2452-2461
10/01/2005
DOI: 10.1182/blood-2005-02-0734
PMID: 15972450
Abstract
AbstractEctopic expression of c-Myc (Myc) in most primary cell types results in programmed cell death, and malignant transformation cannot occur without additional mutations that block apoptosis. The development of Myc-induced lymphoid tumors has been well studied and supports this model. Myc can be upregulated in acute myeloid leukemia (AML), but its exact role in myeloid leukemogenesis is unclear. To study its role in AML, we used a murine stem cell virus (MSCV) retroviral gene transfer/transplantation system to broadly express Myc in the bone marrow of mice either alone or in combination with antiapoptotic mutations. Myc expression in the context either of Arf/Ink4a loss or Bcl-2 coexpression induced a mixture of acute myeloid and acute lymphoid leukemias (AML+ALL). In the absence of antiapoptotic mutations however, all mice transplanted with MSCV-Myc (100%, n = 110) developed AML exclusively. MSCV-Myc-induced AML was polyclonal, readily transplantable, possessed an intact Arf-p53 pathway, and did not display cytogenetic abnormalities by spectral karyotyping (SKY) analysis. Lastly, we found that Myc preferentially stimulated the growth of myeloid progenitor cells in methylcellulose. These data provide the first direct evidence that Myc is a critical downstream effector of myeloid leukemogenesis and suggest that myeloid progenitors are intrinsically resistant to Myc-induced apoptosis. (Blood. 2005;106: 2452-2461)
Details
- Title: Subtitle
- c-Myc rapidly induces acute myeloid leukemia in mice without evidence of lymphoma-associated antiapoptotic mutations
- Creators
- Hui Luo - From the Department of Medicine and Genetics, Division of Oncology, and the Department of Pathology, Washington University School of Medicine, St Louis, MO; and the Department of Hematology/Oncology, University of Chicago, ILQing Li - From the Department of Medicine and Genetics, Division of Oncology, and the Department of Pathology, Washington University School of Medicine, St Louis, MO; and the Department of Hematology/Oncology, University of Chicago, ILJulie O'Neal - From the Department of Medicine and Genetics, Division of Oncology, and the Department of Pathology, Washington University School of Medicine, St Louis, MO; and the Department of Hematology/Oncology, University of Chicago, ILFriederike Kreisel - From the Department of Medicine and Genetics, Division of Oncology, and the Department of Pathology, Washington University School of Medicine, St Louis, MO; and the Department of Hematology/Oncology, University of Chicago, ILMichelle M Le Beau - From the Department of Medicine and Genetics, Division of Oncology, and the Department of Pathology, Washington University School of Medicine, St Louis, MO; and the Department of Hematology/Oncology, University of Chicago, ILMichael H Tomasson - From the Department of Medicine and Genetics, Division of Oncology, and the Department of Pathology, Washington University School of Medicine, St Louis, MO; and the Department of Hematology/Oncology, University of Chicago, IL
- Resource Type
- Journal article
- Publication Details
- Blood, Vol.106(7), pp.2452-2461
- DOI
- 10.1182/blood-2005-02-0734
- PMID
- 15972450
- ISSN
- 0006-4971
- eISSN
- 1528-0020
- Language
- English
- Date published
- 10/01/2005
- Academic Unit
- Hematology, Oncology, and Blood & Marrow Transplantation; Internal Medicine
- Record Identifier
- 9984094542202771
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