Clonal analysis of TET2 and JAK2 mutations suggests that TET2 can be a late event in the progression of myeloproliferative neoplasms

被引:132
作者
Schaub, Franz X. [1 ]
Looser, Renate [1 ]
Li, Sai [1 ]
Hui Hao-Shen [1 ]
Lehmann, Thomas [2 ]
Tichelli, Andre [3 ]
Skoda, Radek C. [1 ]
机构
[1] Univ Basel Hosp, Dept Biomed, CH-4031 Basel, Switzerland
[2] Univ Basel Hosp, Dept Hematol, CH-4031 Basel, Switzerland
[3] Univ Basel Hosp, Div Diagnost Hematol, CH-4031 Basel, Switzerland
基金
瑞士国家科学基金会;
关键词
WORLD-HEALTH-ORGANIZATION; ACUTE MYELOID-LEUKEMIA; POLYCYTHEMIA-VERA; MALIGNANCIES; DISORDERS; T(10/11)(Q22; Q23); CLASSIFICATION; JAK2-V617F; RATIONALE; HAPLOTYPE;
D O I
10.1182/blood-2009-09-245381
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Somatic mutations in TET2 occur in patients with myeloproliferative neoplasms and other hematologic malignancies. It has been suggested that TET2 is a tumor suppressor gene and mutations in TET2 precede the acquisition of JAK2-V617F. To examine the order of events, we performed colony assays and genotyped TET2 and JAK2 in individual colonies. In 4 of 8 myeloproliferative neoplasm patients, we found that some colonies with mutated TET2 carried wild-type JAK2, whereas others were JAK2-V617F positive, indicating that TET2 occurred before JAK2-V617F. One of these patients carried a germline TET2 mutation. However, in 2 other patients, we obtained data compatible with the opposite order of events, with JAK2 exon 12 mutation preceding TET2 mutation in one case. Finally, in 2 of 8 patients, the TET2 and JAK2-V617F mutations defined 2 separate clones. The lack of a strict temporal order of occurrence makes it unlikely that mutations in TET2 represent a predisposing event for acquiring mutations in JAK2. (Blood. 2010; 115: 2003-2007)
引用
收藏
页码:2003 / 2007
页数:5
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