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Calpain-1 inhibitors for selective treatment of rheumatoid arthritis: What is the future?

机译:Calpain-1抑制剂可选择性治疗类风湿关节炎:未来会怎样?

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Effective small-molecule treatment of inflammatory diseases remains an unmet need in medicine. Current treatments are either limited in effectiveness or invasive. The latest biologics prevent influx of inflammatory cells to damaged tissue. Calpain-1 is a calcium-activated cysteine protease that plays an important role in neutrophil motility. It is, therefore, a potential target for intervention in inflammatory disease. Many inhibitors of calpains have been developed but most are unselective and so unsuitable for drug use. However, recent series of α-mercaptoacrylate inhibitors target regulatory domains of calpain-1 and are much more specific. These compounds are effective in impairing the cell spreading mechanism of neutrophils in vitro and raise the possibility of treating rheumatoid arthritis with a pill; however, challenges still remain. Improved bioavailability is needed and solution of their precise mode of action should prompt the development of specific calpain-1 screens for novel classes of inhibitors.
机译:有效的小分子治疗炎性疾病仍然是医学上尚未满足的需求。当前的治疗要么效果有限要么是侵入性的。最新的生物制剂可防止炎症细胞流入受损组织。钙蛋白酶-1是一种钙激活的半胱氨酸蛋白酶,在嗜中性粒细胞运动中起重要作用。因此,它是干预炎症性疾病的潜在目标。已经开发了许多钙蛋白酶抑制剂,但大多数是非选择性的,因此不适合用于药物使用。但是,最近的一系列α-巯基丙烯酸酯抑制剂靶向calpain-1的调节域,并且更具特异性。这些化合物有效地在体外损害中性粒细胞的细胞扩散机制,并增加了用药治疗类风湿性关节炎的可能性。但是,挑战仍然存在。需要提高生物利用度,解决其精确作用方式应促使开发针对新型抑制剂的特定钙蛋白酶-1筛选剂。

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