Mutations of the myeloid transcription factor CEBPA are not associated with the blast crisis of chronic myeloid leukaemia

被引:8
|
作者
Pabst, T
Stillner, E
Neuberg, D
Nimer, S
Willman, CL
List, AF
Melo, JV
Tenen, DG
Mueller, BU
机构
[1] Harvard Univ, Sch Med, Inst Med, Boston, MA 02115 USA
[2] Univ Hosp Bern, Inst Med Oncol, CH-3010 Bern, Switzerland
[3] Dana Farber Canc Inst, Dept Biostat, Boston, MA 02115 USA
[4] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
[5] Univ New Mexico, Sch Med, Albuquerque, NM 87131 USA
[6] Univ S Florida, Coll Med, H Lee Moffitt Canc Ctr & Res Inst, Tampa, FL 33612 USA
[7] Hammersmith Hosp, Imperial Coll, Dept Hematol, London, England
[8] Univ Hosp Bern, Dept Internal Med, CH-3010 Bern, Switzerland
关键词
CEBPA; chronic myeloid leukaemia; transcription factor; differentiation; mutation;
D O I
10.1111/j.1365-2141.2006.06057.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The transcription factor CEBPA is crucial for normal myeloid differentiation. CEBPA gene mutations have been reported in patients with acute myeloid leukaemia. The inevitable evolution of chronic myeloid leukaemia (CML) in chronic phase (CP) to a fatal blast crisis (BC) is assumed to result from the acquisition of additional genetic changes in the leukaemic clone. Gain of CEBPA mutations might represent a key event causing the differentiation block observed in myeloid CML-BC, but not in CML-CP. Here, no CEBPA mutation in 95 CML-BC patients was found, suggesting a limited role, if any, of CEBPA mutations in this disorder.
引用
收藏
页码:400 / 402
页数:3
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