Panani Anna D
Critical Care Department, Cytogenetics Unit, Medical School of Athens University, Evangelismos Hospital, Ipsilandou 45-47, Athens 10676, Greece.
Cancer Lett. 2009 Oct 18;284(1):7-14. doi: 10.1016/j.canlet.2009.02.010. Epub 2009 Mar 9.
The chronic myeloproliferative disorders (CMPD) are a group of clinically related diseases characterized by clonal hematopoiesis with increased proliferation of one or more myeloid cell lineages. The identification of JAK2 mutations (JAK2V617F and JAK2 exon 12) in patients with CMPD is of great significance in the understanding of the molecular mechanisms underlined the pathogenesis of the disease contributing also to clinical management of patients. However, the precise pathogenetic contribution of JAK2 mutation is far from being fully elucidated and it is currently under intense investigation. Testing of JAK2 mutations has made the diagnosis of CMPD more precise than ever before, while genotype-phenotype associations have been identified. Furthermore, the discovery of JAK2 mutations facilitated the development of new targeted therapies and clinical trials are currently ongoing.
慢性骨髓增殖性疾病(CMPD)是一组临床相关疾病,其特征为克隆性造血,伴有一个或多个髓系细胞谱系增殖增加。在CMPD患者中鉴定JAK2突变(JAK2V617F和JAK2第12外显子)对于理解该疾病发病机制的分子机制具有重要意义,这也有助于患者的临床管理。然而,JAK2突变的确切致病作用远未完全阐明,目前正在深入研究。JAK2突变检测使CMPD的诊断比以往任何时候都更加精确,同时已经确定了基因型与表型的关联。此外,JAK2突变的发现促进了新靶向治疗方法的开发,目前临床试验正在进行中。