Suppr超能文献

JAK1选择性抑制剂的研究进展。

Progress toward JAK1-selective inhibitors.

作者信息

Menet Christel J, Mammoliti Oscar, López-Ramos Miriam

机构信息

Department of Medicinal Chemistry, Generaal de Wittelaan L11A3, 2800 Mechelen, Belgium.

出版信息

Future Med Chem. 2015;7(2):203-35. doi: 10.4155/fmc.14.149.

Abstract

The discovery of the JAK-STAT pathway was a landmark in cell biology. The identification of these pathways has changed the landscape of treatment of rheumatoid arthritis and other autoimmune diseases. The two first (unselective) JAK inhibitors have recently been approved by the US FDA for the treatment of myelofibrosis and rheumatoid arthritis and many other JAK inhibitors are currently in clinical development or at the discovery stage. Research groups have demonstrated the different roles of JAK member and the therapeutic potential of targeting them selectively. JAK1 plays a critical and potentially dominant role in the transduction of γc cytokine (γc = common γ chain) and in IL-6 signaling. In this review, we will discuss the state-of-the-art research that evokes JAK1 selective inhibition.

摘要

JAK-STAT信号通路的发现是细胞生物学领域的一个里程碑。这些信号通路的确定改变了类风湿关节炎和其他自身免疫性疾病的治疗格局。首批两种(非选择性)JAK抑制剂最近已获美国食品药品监督管理局批准用于治疗骨髓纤维化和类风湿关节炎,目前还有许多其他JAK抑制剂正处于临床开发或发现阶段。研究团队已经证明了JAK家族成员的不同作用以及选择性靶向它们的治疗潜力。JAK1在γc细胞因子(γc = 共同γ链)的转导以及IL-6信号传导中发挥关键且可能占主导的作用。在本综述中,我们将讨论引发JAK1选择性抑制的最新研究情况。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验