The roles of FLT3 in hematopoiesis and leukemia

被引:1190
作者
Gilliland, DG
Griffin, JD
机构
[1] Harvard Univ, Brigham & Womens Hosp, Sch Med, Howard Hughes Med Inst, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dana Farber Canc Inst, Boston, MA 02115 USA
关键词
D O I
10.1182/blood-2002-02-0492
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
FLT3 is a receptor tyrosine kinase expressed by immature hematopoietic cells and is important for the normal development of stem cells and the immune system. The ligand for FLT3 is expressed by marrow stromal cells and other cells and synergizes with other growth factors to stimulate proliferation of stem cells, progenitor cells, dendritic cells, and natural killer cells. Mutations of FLT3 have been detected in about 30% of patients with acute myelogenous leukemia and a small number of patients with acute lymphocytic leukemia or myelodysplastic syndrome. Patients with FLT3 mutations tend to have a poor prognosis. The mutations most often involve small tandem duplications of amino acids within the juxtamembrane domain of the receptor and result in constitutive tyrosine kinase activity. Expression of a mutant FLT3 receptor in murine marrow cells results in a lethal myeloproliferative syndrome and preliminary studies suggest that mutant FLT3 cooperates with other leukemia oncogenes to confer a more aggressive phenotype. Taken together, these results suggest that FLT3 is an attractive therapeutic target for kinase inhibitors or other approaches for patients with mutations of this gene. (C) 2002 by The American Society of Hematology.
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收藏
页码:1532 / 1542
页数:11
相关论文
共 151 条
  • [81] LYMAN SD, 1994, STEM CELLS, V12, P99
  • [82] Flt3 ligand induces tumor regression and antitumor immune responses in vivo
    Lynch, DH
    Andreasen, A
    Maraskovsky, E
    Whitmore, J
    Miller, RE
    Schuh, JCL
    [J]. NATURE MEDICINE, 1997, 3 (06) : 625 - 631
  • [83] TARGETED DISRUPTION OF THE FLK2/FLT3 GENE LEADS TO DEFICIENCIES IN PRIMITIVE HEMATOPOIETIC PROGENITORS
    MACKAREHTSCHIAN, K
    HARDIN, JD
    MOORE, KA
    BOAST, S
    GOFF, SP
    LEMISCHKA, IR
    [J]. IMMUNITY, 1995, 3 (01) : 147 - 161
  • [84] In vivo generation of human dendritic cell subsets by Flt3 ligand
    Maraskovsky, E
    Daro, E
    Roux, E
    Teepe, M
    Maliszewski, CR
    Hoek, J
    Caron, D
    Lebsack, ME
    McKenna, HJ
    [J]. BLOOD, 2000, 96 (03) : 878 - 884
  • [85] Dramatic increase in the numbers of functionally mature dendritic cells in Flt3 ligand-treated mice: Multiple dendritic cell subpopulations identified
    Maraskovsky, E
    Brasel, K
    Teepe, M
    Roux, ER
    Lyman, SD
    Shortman, K
    McKenna, HJ
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 184 (05) : 1953 - 1962
  • [86] SHC and SHIP phosphorylation and interaction in response to activation of the FLT3 receptor
    Marchetto, S
    Fournier, E
    Beslu, N
    Aurran-Schleinitz, T
    Dubreuil, P
    Borg, JP
    Birnbaum, D
    Rosnet, O
    [J]. LEUKEMIA, 1999, 13 (09) : 1374 - 1382
  • [87] MAROC N, 1993, ONCOGENE, V8, P909
  • [88] A RECEPTOR TYROSINE KINASE SPECIFIC TO HEMATOPOIETIC STEM AND PROGENITOR CELL-ENRICHED POPULATIONS
    MATTHEWS, W
    JORDAN, CT
    WIEGAND, GW
    PARDOLL, D
    LEMISCHKA, IR
    [J]. CELL, 1991, 65 (07) : 1143 - 1152
  • [89] Mice lacking flt3 ligand have deficient hematopoiesis affecting hematopoietic progenitor cells, dendritic cells, and natural killer cells
    McKenna, HJ
    Stocking, KL
    Miller, RE
    Brasel, K
    De Smedt, T
    Maraskovsky, E
    Maliszewski, CR
    Lynch, DH
    Smith, J
    Pulendran, B
    Roux, ER
    Teepe, M
    Lyman, SD
    Peschon, JJ
    [J]. BLOOD, 2000, 95 (11) : 3489 - 3497
  • [90] McKenna HJ, 1996, EXP HEMATOL, V24, P378