Human Oncology and Pathogenesis Program, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10065, USA.
Hematol Oncol Clin North Am. 2012 Oct;26(5):1053-64. doi: 10.1016/j.hoc.2012.07.006. Epub 2012 Aug 21.
Since the discovery of activating mutations in JAK2 in patients with myeloproliferative neoplasms (MPNs) in 2005, gene discovery efforts have identified additional disease alleles, which can predate or occur subsequent to acquisition of JAK2/MPL mutations. In 2009, somatic copy number loss and mutations in the genes TET2 and ASXL1 were identified in MPN patients. Genetic analysis of MPN patient cohorts with adequate sample size and clear clinical annotation are needed to understand the importance of these mutations on MPN phenotype, risk of transformation to leukemia, response to therapy, and influence on overall survival.
自 2005 年在骨髓增殖性肿瘤(MPN)患者中发现 JAK2 激活突变以来,基因发现工作已经确定了其他疾病等位基因,这些等位基因可以先于或后于 JAK2/MPL 突变获得。2009 年,在 MPN 患者中发现了 TET2 和 ASXL1 基因的体细胞拷贝数缺失和突变。需要对具有足够样本量和明确临床注释的 MPN 患者队列进行遗传分析,以了解这些突变对 MPN 表型、向白血病转化的风险、对治疗的反应以及对总生存的影响的重要性。