A role for RUNX1 in hematopoiesis and myeloid leukemia

被引:0
作者
Motoshi Ichikawa
Akihide Yoshimi
Masahiro Nakagawa
Nahoko Nishimoto
Naoko Watanabe-Okochi
Mineo Kurokawa
机构
[1] The University of Tokyo,Department of Hematology and Oncology, Graduate School of Medicine
来源
International Journal of Hematology | 2013年 / 97卷
关键词
RUNX1; Hematopoiesis; Leukemia; Hematopoietic stem cells; Megakaryocytes;
D O I
暂无
中图分类号
学科分类号
摘要
Since its discovery from a translocation in leukemias, the runt-related transcription factor 1/acute myelogenous leukemia-1 (RUNX1/AML1), which is widely expressed in hematopoietic cells, has been extensively studied. Many lines of evidence have shown that RUNX1 plays a critical role in regulating the development and precise maintenance of mammalian hematopoiesis. Studies using knockout mice have shown the importance of RUNX1 in a wide variety of hematopoietic cells, including hematopoietic stem cells and megakaryocytes. Recently, target molecular processes of RUNX1 in normal and malignant hematopoiesis have been revealed. Although RUNX1 is not required for the maintenance of hematopoietic stem cells, it is required for the homeostasis of hematopoietic stem and progenitor cells, and expansion of hematopoietic stem and progenitor cells due to RUNX1 deletion may be an important cause of human leukemias. Molecular abnormalities cooperating with loss of RUNX1 have also been identified. These findings may lead to a further understanding of human leukemias, and suggest novel molecular targeted therapies in the near future.
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页码:726 / 734
页数:8
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[1]  
North TE(2004)Runx1 is expressed in adult mouse hematopoietic stem cells and differentiating myeloid and lymphoid cells, but not in maturing erythroid cells Stem Cells 22 158-168
[2]  
Stacy T(1993)Identification of AML-1 and the (8;21) translocation protein (AML-1/ETO) as sequence-specific DNA-binding proteins: the runt homology domain is required for DNA binding and protein–protein interactions Mol Cell Biol 13 6336-6345
[3]  
Matheny CJ(1996)AML1, the target of multiple chromosomal translocations in human leukemia, is essential for normal fetal liver hematopoiesis Cell 84 321-330
[4]  
Speck NA(1996)Disruption of the Cbfa2 gene causes necrosis and hemorrhaging in the central nervous system and blocks definitive hematopoiesis Proc Natl Acad Sci USA 93 3444-3449
[5]  
de Bruijn MF(2000)A role for hematopoietic stem cells in promoting angiogenesis Cell 102 199-209
[6]  
Meyers S(2009)Runx1 is required for the endothelial to haematopoietic cell transition but not thereafter Nature 457 887-891
[7]  
Downing JR(2010)In vivo imaging of haematopoietic cells emerging from the mouse aortic endothelium Nature 464 116-120
[8]  
Hiebert SW(2004)AML-1 is required for megakaryocytic maturation and lymphocytic differentiation, but not for maintenance of hematopoietic stem cells in adult hematopoiesis Nat Med 10 299-304
[9]  
Okuda T(2005)Loss of Runx1 perturbs adult hematopoiesis and is associated with a myeloproliferative phenotype Blood 106 494-504
[10]  
van Deursen J(2006)AML1 deletion in adult mice causes splenomegaly and lymphomas Oncogene 25 929-939