Squalamine lactate for exudative age-related macular degeneration.

Brian Connolly, Avinash Desai, Charles A Garcia, Edgar Thomas, Michael J Gast
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引用次数: 29

Abstract

Squalamine lactate inhibits angiogenesis by a long-lived, intracellular mechanism of action. The drug is taken up into activated endothelial cells through caveolae, small invaginations in the cellular membrane. Subsequently, the drug binds to and "chaperones" calmodulin to an intracellular membrane compartment and blocks angiogenesis at several levels. A series of basic investigations, preclinical studies, and human clinical trials have begun to establish the proof of concept, efficacy, and safety parameters for use of squalamine lactate as a therapeutic agent for exudative age-related macular degeneration and several types of malignancies.

乳酸角鲨胺治疗渗出性老年性黄斑变性。
乳酸角鲨胺通过长期的细胞内作用机制抑制血管生成。药物通过小泡(细胞膜上的小内陷)进入活化的内皮细胞。随后,该药物与钙调蛋白结合并“陪伴”到细胞膜内腔室,并在几个水平上阻断血管生成。一系列的基础调查、临床前研究和人体临床试验已经开始建立乳酸角鲨胺作为渗出性年龄相关性黄斑变性和几种恶性肿瘤治疗剂的概念、疗效和安全性参数的证明。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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