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细胞黏附分子作为动脉粥样硬化的药物靶点。

Cell adhesion molecules as pharmaceutical target in atherosclerosis.

机构信息

Department of Medicine, Monash University Central Clinical School, Alfred Centre, 99 Commercial Road, Prahran, Melbourne, Victoria 3181, Australia.

出版信息

Mini Rev Med Chem. 2012 Feb;12(2):175-83. doi: 10.2174/138955712798995057.

Abstract

Cell adhesion molecules (CAMs) are transmembrane proteins that mediate adhesion and interactions between cells or cell and extra-cellular matrix. Increased expression and activation of CAMs in vascular endothelial cells and circulating leukocytes, as occurring in the settings of inflammation, hypercholesterolemia, hypertension and diabetes, stimulates leukocyte recruitment into the vascular endothelium, an important step in the pathogenesis of atherosclerosis. CAMs are a potential therapeutic target in clinical practice and in recent years pharmaceutical agents with specific effects on the production and function of these molecules have been studied and developed. This article reviews recent progress regarding pathophysiology of CAMs in atherogenesis and pharmaceutical products or chemicals that are active against CAMs, and assesses the possibilities for clinical developments in this area that might enhance the prevention, monitoring and treatment of atherosclerotic cardiovascular diseases.

摘要

细胞黏附分子(CAMs)是一种跨膜蛋白,介导细胞间或细胞与细胞外基质间的黏附和相互作用。在炎症、高胆固醇血症、高血压和糖尿病等情况下,血管内皮细胞和循环白细胞中 CAM 的表达和激活增加,刺激白细胞招募到血管内皮中,这是动脉粥样硬化发病机制中的一个重要步骤。CAM 是临床实践中的一个潜在治疗靶点,近年来,已经研究和开发了针对这些分子的产生和功能具有特定作用的药物制剂。本文综述了 CAM 在动脉粥样形成中的病理生理学以及针对 CAM 的药物制剂或化学物质方面的最新进展,并评估了在这一领域可能增强动脉粥样硬化性心血管疾病的预防、监测和治疗的临床发展的可能性。

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