College of Biological Science and Engineering, Fuzhou University, Fuzhou, Fujian, 350116, China.
College of Chemistry, Fuzhou University, Fujian, 350116, China.
Drug Discov Today. 2021 Apr;26(4):1076-1085. doi: 10.1016/j.drudis.2021.01.016. Epub 2021 Jan 21.
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.
尿激酶型纤溶酶原激活物受体(uPAR)介导多种生物学活性,在包括恶性肿瘤和炎症在内的几种临床病症中具有关键作用,因此在过去几十年中引起了广泛的研究关注。uPAR 的多效性功能归因于其与一系列配体的相互作用。已经开发出许多抑制剂来干预 uPAR 与其配体的相互作用。在这里,我们回顾了这些 uPAR 抑制剂类别的发展及其抑制机制,以促进这些抑制剂向临床应用的转化。