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致癌性 CSF3R 突变在慢性中性粒细胞白血病和非典型 CML 中的作用。

Oncogenic CSF3R mutations in chronic neutrophilic leukemia and atypical CML.

机构信息

Division of Hematology and Medical Oncology, Knight Cancer Institute, Oregon Health and Science University, Portland, OR 97239, USA.

出版信息

N Engl J Med. 2013 May 9;368(19):1781-90. doi: 10.1056/NEJMoa1214514.

Abstract

BACKGROUND

The molecular causes of many hematologic cancers remain unclear. Among these cancers are chronic neutrophilic leukemia (CNL) and atypical (BCR-ABL1-negative) chronic myeloid leukemia (CML), both of which are diagnosed on the basis of neoplastic expansion of granulocytic cells and exclusion of genetic drivers that are known to occur in other myeloproliferative neoplasms and myeloproliferative-myelodysplastic overlap neoplasms.

METHODS

To identify potential genetic drivers in these disorders, we used an integrated approach of deep sequencing coupled with the screening of primary leukemia cells obtained from patients with CNL or atypical CML against panels of tyrosine kinase-specific small interfering RNAs or small-molecule kinase inhibitors. We validated candidate oncogenes using in vitro transformation assays, and drug sensitivities were validated with the use of assays of primary-cell colonies.

RESULTS

We identified activating mutations in the gene encoding the receptor for colony-stimulating factor 3 (CSF3R) in 16 of 27 patients (59%) with CNL or atypical CML. These mutations segregate within two distinct regions of CSF3R and lead to preferential downstream kinase signaling through SRC family-TNK2 or JAK kinases and differential sensitivity to kinase inhibitors. A patient with CNL carrying a JAK-activating CSF3R mutation had marked clinical improvement after the administration of the JAK1/2 inhibitor ruxolitinib.

CONCLUSIONS

Mutations in CSF3R are common in patients with CNL or atypical CML and represent a potentially useful criterion for diagnosing these neoplasms. (Funded by the Leukemia and Lymphoma Society and others.).

摘要

背景

许多血液系统恶性肿瘤的分子病因仍然不明。其中包括慢性中性粒细胞白血病(CNL)和非典型(BCR-ABL1 阴性)慢性髓性白血病(CML),这两种疾病均基于粒细胞的肿瘤性扩张以及排除已知发生于其他骨髓增殖性肿瘤和骨髓增生性-骨髓发育不良重叠肿瘤中的遗传驱动因素而诊断。

方法

为了确定这些疾病中的潜在遗传驱动因素,我们采用了一种整合方法,即深度测序与针对 CNL 或非典型 CML 患者的原代白血病细胞进行的酪氨酸激酶特异性小干扰 RNA 或小分子激酶抑制剂筛选相结合。我们使用体外转化测定法验证候选癌基因,并用原代细胞集落测定法验证药物敏感性。

结果

我们在 27 例 CNL 或非典型 CML 患者中的 16 例(59%)中鉴定出了集落刺激因子 3 受体(CSF3R)基因的激活突变。这些突变在 CSF3R 的两个不同区域内发生,导致通过 SRC 家族-TNK2 或 JAK 激酶优先进行下游激酶信号传导,并对激酶抑制剂具有不同的敏感性。携带 JAK 激活 CSF3R 突变的 CNL 患者在接受 JAK1/2 抑制剂芦可替尼治疗后,临床状况显著改善。

结论

CSF3R 突变在 CNL 或非典型 CML 患者中很常见,代表了诊断这些肿瘤的潜在有用标准。(由白血病和淋巴瘤协会及其他组织资助)。

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