Division of Hematology/Oncology, Cancer Research Institute, Beth Israel Deaconess Medical Center, Boston, Massachusetts.
National Research Center for Radiation Medicine, Kyiv, Ukraine.
Am J Hematol. 2019 Jan;94(1):62-73. doi: 10.1002/ajh.25307. Epub 2018 Oct 31.
Myeloproliferative neoplasms (MPNs) driver mutations are usually found in JAK2, MPL, and CALR genes; however, 10%-15% of cases are triple negative (TN). A previous study showed lower rate of JAK2 V617F in primary myelofibrosis patients exposed to low doses of ionizing radiation (IR) from Chernobyl accident. To examine distinct driver mutations, we enrolled 281 Ukrainian IR-exposed and unexposed MPN patients. Genomic DNA was obtained from peripheral blood leukocytes. JAK2 V617F, MPL W515, types 1- and 2-like CALR mutations were identified by Sanger Sequencing and real time polymerase chain reaction. Chromosomal alterations were assessed by oligo-SNP microarray platform. Additional genetic variants were identified by whole exome and targeted sequencing. Statistical significance was evaluated by Fisher's exact test and Wilcoxon's rank sum test (R, version 3.4.2). IR-exposed MPN patients exhibited a different genetic profile vs unexposed: lower rate of JAK2 V617F (58.4% vs 75.4%, P = .0077), higher rate of type 1-like CALR mutation (12.2% vs 3.1%, P = .0056), higher rate of TN cases (27.8% vs 16.2%, P = .0366), higher rate of potentially pathogenic sequence variants (mean numbers: 4.8 vs 3.1, P = .0242). Furthermore, we identified several potential drivers specific to IR-exposed TN MPN patients: ATM p.S1691R with copy-neutral loss of heterozygosity at 11q; EZH2 p.D659G at 7q and SUZ12 p.V71 M at 17q with copy number loss. Thus, IR-exposed MPN patients represent a group with distinct genomic characteristics worthy of further study.
骨髓增殖性肿瘤(MPN)的驱动突变通常发生在 JAK2、MPL 和 CALR 基因中;然而,10%-15%的病例为三阴性(TN)。先前的研究表明,暴露于切尔诺贝利事故低剂量电离辐射(IR)的原发性骨髓纤维化患者中 JAK2 V617F 的发生率较低。为了检查不同的驱动突变,我们招募了 281 名乌克兰 IR 暴露和未暴露的 MPN 患者。从外周血白细胞中提取基因组 DNA。通过 Sanger 测序和实时聚合酶链反应鉴定 JAK2 V617F、MPL W515、1 型和 2 型 CALR 突变。通过寡核苷酸 SNP 微阵列平台评估染色体改变。通过全外显子组和靶向测序鉴定其他遗传变异。通过 Fisher 精确检验和 Wilcoxon 秩和检验(R,版本 3.4.2)评估统计学意义。IR 暴露的 MPN 患者表现出与未暴露患者不同的遗传特征:JAK2 V617F 发生率较低(58.4%对 75.4%,P =.0077),1 型 CALR 突变发生率较高(12.2%对 3.1%,P =.0056),TN 病例发生率较高(27.8%对 16.2%,P =.0366),潜在致病性序列变异发生率较高(平均值:4.8 对 3.1,P =.0242)。此外,我们还鉴定了几个特定于 IR 暴露的 TN MPN 患者的潜在驱动基因:ATM p.S1691R 伴 11q 杂合性缺失;EZH2 p.D659G 在 7q 和 SUZ12 p.V71 M 在 17q 伴有拷贝数缺失。因此,IR 暴露的 MPN 患者代表一组具有独特基因组特征的患者,值得进一步研究。