Cardiovascular Pathobiology Program, Diabetes and Obesity Research Center, Sanford Burnham Prebys Medical Discovery Institute, Orlando, Florida, United States of America.
Conrad Prebys Center for Chemical Genomics, Sanford Burnham Prebys Medical Discovery Institute, Orlando, Florida, United States of America.
PLoS One. 2018 Sep 12;13(9):e0202436. doi: 10.1371/journal.pone.0202436. eCollection 2018.
Neovascularization is the pathological driver of blinding eye diseases such as retinopathy of prematurity, proliferative diabetic retinopathy, and wet age-related macular degeneration. The loss of vision resulting from these diseases significantly impacts the productivity and quality of life of patients, and represents a substantial burden on the health care system. Current standard of care includes biologics that target vascular endothelial growth factor (VEGF), a key mediator of neovascularization. While anti-VGEF therapies have been successful, up to 30% of patients are non-responsive. Therefore, there is a need for new therapeutic targets, and small molecule inhibitors of angiogenesis to complement existing treatments. Apelin and its receptor have recently been shown to play a key role in both developmental and pathological angiogenesis in the eye. Through a cell-based high-throughput screen, we identified 4-aminoquinoline antimalarial drugs as potent selective antagonists of APJ. The prototypical 4-aminoquinoline, amodiaquine was found to be a selective, non-competitive APJ antagonist that inhibited apelin signaling in a concentration-dependent manner. Additionally, amodiaquine suppressed both apelin-and VGEF-induced endothelial tube formation. Intravitreal amodaiquine significantly reduced choroidal neovascularization (CNV) lesion volume in the laser-induced CNV mouse model, and showed no signs of ocular toxicity at the highest doses tested. This work firmly establishes APJ as a novel, chemically tractable therapeutic target for the treatment of ocular neovascularization, and that amodiaquine is a potential candidate for repurposing and further toxicological, and pharmacokinetic evaluation in the clinic.
血管新生是导致早产儿视网膜病变、增生性糖尿病视网膜病变和湿性年龄相关性黄斑变性等致盲眼病的病理驱动因素。这些疾病导致的视力丧失,严重影响了患者的生产力和生活质量,也给医疗保健系统带来了巨大的负担。目前的治疗标准包括针对血管内皮生长因子(VEGF)的生物制剂,VEGF 是血管新生的关键介质。虽然抗 VEGF 疗法已经取得了成功,但多达 30%的患者没有反应。因此,需要新的治疗靶点和血管生成的小分子抑制剂来补充现有的治疗方法。阿皮林及其受体最近被证明在眼部的发育和病理性血管新生中发挥关键作用。通过基于细胞的高通量筛选,我们发现 4-氨基喹啉类抗疟药物是 APJ 的有效、选择性拮抗剂。原型 4-氨基喹啉阿莫地喹被发现是一种选择性、非竞争性的 APJ 拮抗剂,能够以浓度依赖的方式抑制阿皮林信号。此外,阿莫地喹还抑制了阿皮林和 VEGF 诱导的内皮管形成。玻璃体内注射阿莫地喹可显著减少激光诱导的脉络膜新生血管(CNV)小鼠模型中的脉络膜新生血管(CNV)病变体积,并且在测试的最高剂量下没有表现出眼部毒性的迹象。这项工作明确确立了 APJ 作为治疗眼部血管新生的一种新的、化学上可处理的治疗靶点,并且阿莫地喹是一种具有重新定位潜力的候选药物,值得在临床上进行进一步的毒理学和药代动力学评估。