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SETBP1 突变发生在 9%的 MDS/MPN 和 4%的 MPN 病例中,与非典型 CML、单体 7、i(17)(q10) 等臂染色体、ASXL1 和 CBL 突变密切相关。

SETBP1 mutations occur in 9% of MDS/MPN and in 4% of MPN cases and are strongly associated with atypical CML, monosomy 7, isochromosome i(17)(q10), ASXL1 and CBL mutations.

机构信息

MLL Munich Leukemia Laboratory, Munich, Germany.

出版信息

Leukemia. 2013 Sep;27(9):1852-60. doi: 10.1038/leu.2013.133. Epub 2013 Apr 30.

Abstract

Chronic myeloid malignancies are categorized to the three main categories myeloproliferative neoplasms (MPNs), myelodysplastic syndromes (MDSs) and MDS/MPN overlap. So far, no specific genetic alteration profiles have been identified in the MDS/MPN overlap category. Recent studies identified mutations in SET-binding protein 1 (SETBP1) as novel marker in myeloid malignancies, especially in atypical chronic myeloid leukemia (aCML) and related diseases. We analyzed SETBP1 in 1 130 patients with MPN and MDS/MPN overlap and found mutation frequencies of 3.8% and 9.4%, respectively. In particular, there was a high frequency of SETBP1 mutation in aCML (19/60; 31.7%) and MDS/MPN unclassifiable (MDS/MPN, U; 20/240; 9.3%). SETBP1 mutated (SETBP1mut) patients showed significantly higher white blood cell counts and lower platelet counts and hemoglobin levels than SETBP1 wild-type patients. Cytomorphologic evaluation revealed a more dysplastic phenotype in SETBP1mut cases as compared with wild-type cases. We confirm a significant association of SETBP1mut with -7 and isochromosome i(17)(q10). Moreover, SETBP1mut were strongly associated with ASXL1 and CBL mutations (P<0.001 for both) and were mutually exclusive of JAK2 and TET2 mutations. In conclusion, SETBP1mut add an important new diagnostic marker for MDS/MPN and in particular for aCML.

摘要

慢性髓系恶性肿瘤可分为三大类

骨髓增殖性肿瘤(MPNs)、骨髓增生异常综合征(MDSs)和 MDS/MPN 重叠。迄今为止,在 MDS/MPN 重叠类别中尚未确定特定的遗传改变谱。最近的研究确定了 SET 结合蛋白 1(SETBP1)突变是髓系恶性肿瘤的新型标志物,尤其是在不典型慢性髓系白血病(aCML)和相关疾病中。我们分析了 1130 例 MPN 和 MDS/MPN 重叠患者的 SETBP1,发现突变频率分别为 3.8%和 9.4%。特别是在 aCML(19/60;31.7%)和 MDS/MPN 无法分类(MDS/MPN,U;20/240;9.3%)中,SETBP1 突变的频率很高。SETBP1 突变(SETBP1mut)患者的白细胞计数明显较高,血小板计数和血红蛋白水平明显较低。细胞形态学评估显示,与野生型病例相比,SETBP1mut 病例的表型更具发育不良。我们证实 SETBP1mut 与-7 和等臂染色体 i(17)(q10)显著相关。此外,SETBP1mut 与 ASXL1 和 CBL 突变强烈相关(均 P<0.001),与 JAK2 和 TET2 突变互斥。总之,SETBP1mut 为 MDS/MPN 特别是 aCML 增加了一个重要的新诊断标志物。

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