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Nf1 deficiency causes Ras-Dediated granulocyte/macrophage colony stimulating factor hypersensitivity and chronic myeloid leukaemia
Abstract
The Ras signal transduction pathway is often deregulated in human myeloid leukaemia. For example, activating point mutations in RAS genes are found in some patients with juvenile chronic myelogenous leukaemia (JCML), while other patients with JCML show loss of the neurofibromatosis type 1 (NF1) gene, a Ras GTPase activating protein. By generating mice whose haematopoietic system is reconsituted with Nf1 deficient haematopoietic stem cells we show that Nf1 gene loss, by itself, is sufficient to produce the myeloproliferative symptoms associated with human JCML. We also provide evidence to indicate that Nf1 gene loss induces myeloproliferative disease through a Ras-mediated hypersensitivity to granulocyte/macrophage-colony stimulating factor (GM-CSF). Finally, we describe a genetic screen for identifying genes that cooperate with Nf1 gene loss during progression to acute myeloid leukaemia.
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“and juvenile myelomonocytic leukemia (6).”
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Chan, G., & Neel, B. G. (2016) · Springer eBooks · doi:10.1007/978-1-4939-3649-6_4 · Cited by 13
Kim, W.-I., Wiesner, S. M., & Largaespada, D. A. (2007) · Experimental Hematology · doi:10.1016/j.exphem.2007.04.012 · Cited by 15
Self-citationIde, L. U. S., Aylor, R. T., Uce, M. I. L., & Hannon, K. E. S. (1997) · Cited by 14
IL-3 receptor signaling is dispensable for BCR-ABL-induced myeloproliferative disease
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Myeloid Leukemia: Disease Genes and Mouse Models
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Self-citationMorgan, K. J., Rowley, M., Wiesner, S. M., Hasz, D. E., Ness, B. V., & Largaespada, D. A. (2007) · Leukemia Research · doi:10.1016/j.leukres.2006.11.022 · Cited by 13
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Metadata
- Authors
- Largaespada, D. A., Brannan, C. I., Jenkins, N. A., & Copeland, N. G.
- Affiliations
- Frederick National Laboratory for Cancer Research (US)
- University of Florida (US)
- Venue
- Nature Genetics
- Published
- 1996-02
- Volume
- 12
- Issue
- 2
- Pages
- 137-143
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W2087533846
- Cited by
- 284
- References
- 33
- Citations by year
- 2025: 2 · 2024: 2 · 2023: 2 · 2022: 1 · 2021: 2 · 2020: 1 · 2019: 6 · 2018: 4 · 2017: 3 · 2016: 8 · 2015: 4 · 2014: 4 · 2013: 6 · 2012: 14
- FWCI
- 15.71
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Genetics (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Clinical Neurology › Neurofibromatosis and Schwannoma Cases
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Tyrosine Phosphatases
- Health Sciences › Medicine › Hematology › Acute Myeloid Leukemia Research
- Keywords
- neurofibromatosis type 1, NF1 deficiency, Ras signaling, GM-CSF, GM-CSF hypersensitivity, chronic myeloid leukemia, myeloproliferative neoplasms, hematopoietic stem cells, genetic screen, Ras GTPase-activating protein
- MeSH terms
- Acute Disease, Animals, Bone Marrow, Cell Differentiation, Cell Line, Transformed, Crosses, Genetic, Disease Models, Animal, Female, Guanosine Triphosphate, Hematopoietic Stem Cells, Humans, Leukemia, Myeloid, Liver, Male, Mice, Inbred C57BL, Signal Transduction, Leukemia, Myelogenous, Chronic, BCR-ABL Positive, Granulocyte-Macrophage Colony-Stimulating Factor, Genes, Neurofibromatosis 1, Hematopoietic Stem Cell Transplantation, Disease Progression, ras Proteins, Mice
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