Department of Medicine; Wilf Family Cardiovascular Research Institute, Albert Einstein College of Medicine, New York, NY, USA.
Department of Molecular Pharmacology, Einstein-Mount Sinai Diabetes Research Center (ES-DRC), The "Norman Fleischer" Institute for Diabetes and Metabolism (FIDAM), Albert Einstein College of Medicine, NY, New York, USA.
Expert Opin Ther Targets. 2020 Jan;24(1):79-88. doi: 10.1080/14728222.2020.1707806. Epub 2020 Jan 15.
: Angiopoietin-like (ANGPTL) proteins belong to a family of eight secreted factors that are structurally related to proteins that modulate angiogenesi, commonly known as angiopoietins. Specifically, ANGPTL3, ANGPTL4, and ANGPTL8 (the 'ANGPT L3-4-8 triad'), have surfaced as principal regulators of plasma lipid metabolism by functioning as potent inhibitors of lipoprotein lipase. The targeting of these proteins may open up future therapeutic avenues for metabolic and cardiovascular disease.: This article systematically summarizes the compelling literature describing the mechanistic roles of ANGPTL3, 4, and 8 in lipid metabolism, emphasizing their importance in determining the risk of cardiovascular disease. We shed light on population-based studies linking loss-of-function variations in ANGPTL3, 4, and 8 with decreased risk of metabolic conditions and cardiovascular disorders. We also discuss how the strategies aiming at targeting the ANGPT L3-4-8 triad could offer therapeutic benefit in the clinical scenario.: Monoclonal antibodies and antisense oligonucleotides that target ANGPTL3, 4, and 8 are potentially an efficient therapeutic strategy for hypertriglyceridemia and cardiovascular risk reduction, especially in patients with limited treatment options. These innovative therapeutical approaches are at an embryonic stage in development and hence further investigations are necessary for eventual use in humans.
血管生成素样(ANGPTL)蛋白属于一个家族的八种分泌因子,它们与调节血管生成的蛋白质在结构上相关,通常被称为血管生成素。具体来说,ANGPTL3、ANGPTL4 和 ANGPTL8(“ANGPTL3-4-8 三联体”)已成为血浆脂质代谢的主要调节剂,作为脂蛋白脂肪酶的有效抑制剂发挥作用。这些蛋白质的靶向可能为代谢和心血管疾病开辟未来的治疗途径。
本文系统地总结了描述 ANGPTL3、4 和 8 在脂质代谢中作用机制的引人注目的文献,强调了它们在确定心血管疾病风险中的重要性。我们探讨了与 ANGPTL3、4 和 8 的功能丧失变异相关的人群研究,这些变异与代谢状况和心血管疾病风险降低有关。我们还讨论了针对 ANGPTL3-4-8 三联体的策略如何在临床情况下提供治疗益处。
针对 ANGPTL3、4 和 8 的单克隆抗体和反义寡核苷酸可能是治疗高甘油三酯血症和降低心血管风险的有效治疗策略,特别是在治疗选择有限的患者中。这些创新的治疗方法尚处于开发的萌芽阶段,因此需要进一步的研究,以便最终在人类中使用。