尿激酶受体
纤溶酶原激活剂
受体
尿激酶
阻塞(统计)
化学
计算生物学
药理学
癌症研究
医学
生物
计算机科学
生物化学
内科学
计算机网络
作者
Cai Yuan,Zhanzhi Guo,Shujuan Yu,Longguang Jiang,Mingdong Huang
标识
DOI:10.1016/j.drudis.2021.01.016
摘要
Urokinase-type plasminogen activator receptor (uPAR) mediates a multitude of biological activities, has key roles in several clinical indications, including malignancies and inflammation, and, thus, has attracted intensive research over the past few decades. The pleiotropic functions of uPAR can be attributed to its interaction with an array of partners. Many inhibitors have been developed to intervene with the interaction of uPAR with these partners. Here, we review the development of these classes of uPAR inhibitor and their inhibitory mechanisms to promote the translation of these inhibitors to clinical applications.
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