Evans Jilly F, Ferguson Andrew D, Mosley Ralph T, Hutchinson John H
Amira Pharmaceuticals, 9535 Waples Street, San Diego, CA 92121, USA.
Trends Pharmacol Sci. 2008 Feb;29(2):72-8. doi: 10.1016/j.tips.2007.11.006. Epub 2008 Jan 9.
Leukotrienes have physiological roles in innate immune responses and pathological roles in inflammatory diseases, such as asthma, allergic rhinitis and atherosclerosis. Anti-leukotriene therapy has proven benefits in the treatment of respiratory disease, either through the inhibition of leukotriene synthesis or the selective antagonism of leukotriene receptors. The first committed step in the synthesis of leukotrienes is the oxidation of arachidonic acid (AA) by 5-lipoxygenase (5-LO), and the integral membrane protein 5-lipoxygenase-activating protein (FLAP) is an essential partner of 5-LO for this process. FLAP was molecularly identified via a photoaffinity probe and an affinity gel based on MK-886, a selective leukotriene inhibitor that has no activity against broken-cell preparations of 5-LO. Several FLAP inhibitors showed efficacy in early clinical trials in asthma but were not developed commercially for unpublished reasons. Recently, the FLAP (ALOX5AP) gene has been linked to risk for myocardial infarction, stroke and restenosis, reigniting pharmaceutical interest in this target. In addition, the recent determination of the crystal structure of inhibitor-bound FLAP offers exciting potential for novel FLAP inhibitor design.
白三烯在先天性免疫反应中具有生理作用,在诸如哮喘、过敏性鼻炎和动脉粥样硬化等炎症性疾病中具有病理作用。抗白三烯疗法已被证明在治疗呼吸道疾病方面具有益处,其作用方式要么是抑制白三烯的合成,要么是选择性拮抗白三烯受体。白三烯合成的首个关键步骤是5-脂氧合酶(5-LO)将花生四烯酸(AA)氧化,而整合膜蛋白5-脂氧合酶激活蛋白(FLAP)是此过程中5-LO的重要伴侣。FLAP是通过一种光亲和探针和基于MK-886的亲和凝胶在分子水平上鉴定出来的,MK-886是一种选择性白三烯抑制剂,对5-LO的破碎细胞制剂无活性。几种FLAP抑制剂在哮喘的早期临床试验中显示出疗效,但由于未公开的原因未进行商业化开发。最近,FLAP(ALOX5AP)基因已与心肌梗死、中风和再狭窄风险相关联,这重新燃起了制药行业对该靶点的兴趣。此外,最近测定的与抑制剂结合的FLAP晶体结构为新型FLAP抑制剂设计提供了令人兴奋的潜力。