Vainchenker William, Dusa Alexandra, Constantinescu Stefan N
Institut Gustave Roussy PR 1, 94805 Villejuif, France.
Semin Cell Dev Biol. 2008 Aug;19(4):385-93. doi: 10.1016/j.semcdb.2008.07.002. Epub 2008 Jul 17.
The four mammalian Janus kinase (JAK) family members, JAK1, JAK2, JAK3 and TYK2, are non-receptor protein tyrosine kinases (PTKs) that are crucial for cytokine receptor signaling in blood formation and immune responses. Mutations and translocations in the JAK genes leading to constitutively active JAK proteins are associated with a variety of hematopoietic malignancies, including the myeloproliferative disorders (JAK2), acute lymphoblastic leukemia (JAK2), acute myeloid leukemia (JAK2, JAK1), acute megakaryoblastic leukemia (JAK2, JAK3) and T-cell precursor acute lymphoblastic leukemia (JAK1). In contrast, loss-of-function mutations of JAK3 and TYK2 lead to immunodeficiency. The role of JAKs as therapeutic targets is starting to expand, as more insights into their structure and activation mechanisms become available.
四种哺乳动物的Janus激酶(JAK)家族成员,即JAK1、JAK2、JAK3和TYK2,是非受体蛋白酪氨酸激酶(PTK),它们在血液形成和免疫反应中的细胞因子受体信号传导中起着关键作用。JAK基因的突变和易位导致组成型活性JAK蛋白,与多种造血系统恶性肿瘤相关,包括骨髓增殖性疾病(JAK2)、急性淋巴细胞白血病(JAK2)、急性髓性白血病(JAK2、JAK1)、急性巨核细胞白血病(JAK2、JAK3)和T细胞前体急性淋巴细胞白血病(JAK1)。相反,JAK3和TYK2的功能丧失突变会导致免疫缺陷。随着对JAKs结构和激活机制的深入了解,JAKs作为治疗靶点的作用开始扩大。