Concurrent MPL515 and JAK2V617F mutations in myelofibrosis:: chronology of clonal emergence and changes in mutant allele burden over time

被引:78
|
作者
Lasho, Terra L.
Pardanani, Animesh
McClure, Rebecca F.
Mesa, Ruben A.
Levine, Ross L.
Gilliland, D. Gary
Tefferi, Ayalew
机构
[1] Mayo Clin, Div Hematol, Rochester, MN 55905 USA
[2] Dana Farber Canc Inst, Rochester, MN USA
[3] Harvard Univ, Sch Med, Brigham & Womens Hosp, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Howard Hughes Med Inst, Boston, MA 02115 USA
关键词
myelofibrosis; MPLW515L; MPLW515K; essential thrombocythaemia;
D O I
10.1111/j.1365-2141.2006.06348.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
MPLW515L/K and JAK2V617F can co-exist in myelofibrosis with myeloid metaplasia (MMM). The chronology of clonal emergence was studied in three such cases using serially stored bone marrow. At diagnosis, a major MPL515 mutant clone was accompanied by a minor JAK2V617F clone in all three instances. At 25 time points over a period of 4-8 years, allele burden fluctuated but remained high for MPLW515L/K and low for JAK2V617F. We conclude that MPLW515L/K and JAK2V617F are both early events in MMM and allele burden, rather than the mere presence of these mutations, might be relevant to phenotypic variation in myeloproliferative disorders.
引用
收藏
页码:683 / 687
页数:5
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