State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica (SIMM), Chinese Academy of Sciences, Shanghai, China.
School of Pharmacy, University of Chinese Academy of Sciences, Beijing, China.
Med Res Rev. 2020 Jan;40(1):79-134. doi: 10.1002/med.21597. Epub 2019 May 29.
Inflammation is thought to play an important role in the pathogenesis of vascular diseases. Lipoprotein-associated phospholipase A2 (Lp-PLA2) mediates vascular inflammation through the regulation of lipid metabolism in blood, thus, it has been extensively investigated to identify its role in vascular inflammation-related diseases, mainly atherosclerosis. Although darapladib, the most advanced Lp-PLA2 inhibitor, failed to meet the primary endpoints of two large phase III trials in atherosclerosis patients cotreated with standard medical care, the research on Lp-PLA2 has not been terminated. Novel pathogenic, epidemiologic, genetic, and crystallographic studies regarding Lp-PLA2 have been reported recently, while novel inhibitors were identified through a fragment-based lead discovery strategy. More strikingly, recent clinical and preclinical studies revealed that Lp-PLA2 inhibition showed promising therapeutic effects in diabetic macular edema and Alzheimer's disease. In this review, we not only summarized the knowledge of Lp-PLA2 established in the past decades but also emphasized new findings in recent years. We hope this review could be valuable for helping researchers acquire a much deeper insight into the nature of Lp-PLA2, identify more potent and selective Lp-PLA2 inhibitors, and discover the potential indications of Lp-PLA2 inhibitors.
炎症被认为在血管疾病的发病机制中起重要作用。脂蛋白相关磷脂酶 A2(Lp-PLA2)通过调节血液中的脂质代谢来介导血管炎症,因此,它已被广泛研究以确定其在与血管炎症相关的疾病中的作用,主要是动脉粥样硬化。尽管在接受标准医疗护理的动脉粥样硬化患者的两项大型 III 期试验中,最先进的 Lp-PLA2 抑制剂 darapladib 未能达到主要终点,但对 Lp-PLA2 的研究并未终止。最近有关于 Lp-PLA2 的新的发病机制、流行病学、遗传学和晶体学研究报告,而通过基于片段的先导发现策略确定了新型抑制剂。更引人注目的是,最近的临床前和临床研究表明,Lp-PLA2 抑制在糖尿病性黄斑水肿和阿尔茨海默病中显示出有希望的治疗效果。在这篇综述中,我们不仅总结了过去几十年中建立的关于 Lp-PLA2 的知识,还强调了近年来的新发现。我们希望这篇综述有助于研究人员更深入地了解 Lp-PLA2 的本质,识别更有效和更具选择性的 Lp-PLA2 抑制剂,并发现 Lp-PLA2 抑制剂的潜在适应证。
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