1] Inflammation Research Center - VIB, Rijvisschestraat 120 9052 Ghent, Belgium. [2] Department of Biomedical Molecular Biology - Ghent University, FSVM Building, Technologiepark 927, B-9052 Zwijnaarde, Ghent, Belgium.
Nat Rev Drug Discov. 2014 Dec;13(12):904-27. doi: 10.1038/nrd4390. Epub 2014 Nov 7.
Matrix metalloproteinases (MMPs) are zinc-dependent endopeptidases that form a family of 24 members in mammals. Evidence of the pathological roles of MMPs in various diseases, combined with their druggability, has made them attractive therapeutic targets. Initial drug discovery efforts focused on the roles of MMPs in cancer progression, and more than 50 MMP inhibitors have been investigated in clinical trials in various cancers. However, all of these trials failed. Reasons for failure include the lack of inhibitor specificity and insufficient knowledge about the complexity of the disease biology. MMPs are also known to be involved in several inflammatory processes, and there are new therapeutic opportunities for MMP inhibitors to treat such diseases. In this Review, we discuss the recent advances made in understanding the role of MMPs in inflammatory diseases and the therapeutic potential of MMP inhibition in those conditions.
基质金属蛋白酶(MMPs)是锌依赖性内肽酶,在哺乳动物中形成一个包含 24 个成员的家族。MMPs 在各种疾病中的病理作用的证据,加上它们的成药性,使它们成为有吸引力的治疗靶点。最初的药物发现工作集中在 MMPs 在癌症进展中的作用上,已有超过 50 种 MMP 抑制剂在各种癌症的临床试验中进行了研究。然而,所有这些试验都失败了。失败的原因包括抑制剂特异性的缺乏和对疾病生物学复杂性的了解不足。MMPs 也已知参与几种炎症过程,因此 MMP 抑制剂在治疗这些疾病方面有新的治疗机会。在这篇综述中,我们讨论了在理解 MMPs 在炎症性疾病中的作用以及 MMP 抑制在这些疾病中的治疗潜力方面的最新进展。