Sayyah Jacqueline, Sayeski Peter P
Department of Physiology and Functional Genomics, University of Florida College of Medicine, 1600 SW Archer Road, Room M552, Gainesville, FL 32610, USA.
Curr Oncol Rep. 2009 Mar;11(2):117-24. doi: 10.1007/s11912-009-0018-2.
Although the Jak2-V617F mutation has generated strong awareness because of its causative role in myeloproliferative disorders, reports of Jak2 gene aberrations linked to hematologic malignancies have preceded those of V617F by nearly a decade. These malignant mutations include Jak2 amino acid substitutions, deletions, insertions, and chromosomal translocations. As a consequence, researchers are increasingly focused on identifying Jak2 inhibitors that suppress aberrant Jak2 kinase activity. Some of these inhibitors may one day become therapeutically beneficial for individuals with Jak2-related hematologic malignancies. This review summarizes various Jak2 mutations associated with hematologic malignancies and assesses some of the Jak2 inhibitors in the preclinical phase or in clinical trials. By reviewing these specific areas, we hope to have a better understanding of Jak2's role in hematologic malignancies and to shed light on the utility of Jak2 inhibitors.
尽管Jak2-V617F突变因其在骨髓增殖性疾病中的致病作用而引起了广泛关注,但与血液系统恶性肿瘤相关的Jak2基因畸变的报道比V617F的报道早了近十年。这些恶性突变包括Jak2氨基酸替换、缺失、插入和染色体易位。因此,研究人员越来越专注于寻找能够抑制异常Jak2激酶活性的Jak2抑制剂。其中一些抑制剂可能有朝一日对患有Jak2相关血液系统恶性肿瘤的个体具有治疗益处。本综述总结了与血液系统恶性肿瘤相关的各种Jak2突变,并评估了一些处于临床前阶段或临床试验中的Jak2抑制剂。通过回顾这些特定领域,我们希望能更好地理解Jak2在血液系统恶性肿瘤中的作用,并阐明Jak2抑制剂的效用。