贾纳斯激酶
JAK-STAT信号通路
酪氨酸激酶2
斯达
Janus激酶1
癌症研究
医学
鲁索利替尼
信号转导
酪氨酸激酶
药理学
生物
细胞因子
受体
免疫学
车站3
内科学
遗传学
血小板源性生长因子受体
生长因子
骨髓
骨髓纤维化
作者
Tong Li,Xianjing Yang,Juan Zhu,Ying Liu,Xiaobao Jin,Gong Chen,Lianbao Ye
标识
DOI:10.1016/j.intimp.2023.110660
摘要
JAK kinase includes four family members: JAK1, JAK2, JAK3, and TYK2. It forms the JAK-STAT pathway with signal transmitters and activators of subscription (STAT). This pathway is one of the main mechanisms by which many cytokine receptors transduce intracellular signals, it is associated with the occurrence of various immune, inflammatory, and tumor diseases. JAK inhibitors block the signal transduction of the JAK-STAT pathway by targeting JAK kinase. Based on whether they target multiple subtypes of JAK kinase, JAK inhibitors are categorized into pan-JAK inhibitors and selective JAK inhibitors. Compared with pan JAK inhibitors, selective JAK inhibitors are associated with a specific member, thus more targeted in therapy, with improved efficacy and reduced side effects. Currently, a number of JAK inhibitors have been approval for disease treatment. This review summarized the current application status of JAK inhibitors that have been marketed, advances of JAK inhibitors currently in phase Ш clinical trials, and the structure-activity relationship of them, with an intention to provide references for the development of novel JAK inhibitors.
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