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RAGE:一种多配体受体,揭示了健康和疾病的新见解。

RAGE: a multi-ligand receptor unveiling novel insights in health and disease.

机构信息

Department of Pharmaceutical Chemistry, School of Pharmacy, Aristotle University of Thessaloniki, 54124 Greece.

出版信息

Curr Med Chem. 2010;17(21):2232-52. doi: 10.2174/092986710791331086.

Abstract

Receptor for advanced glycation end products (RAGE) is expressed in a range of cell types such as endothelial cells, smooth muscle cells, mesangial cells, mononuclear phagocytes and certain neurons. It is a multi-ligand receptor and a member of the immunoglobulin superfamily of cell surface molecules. Its repertoire of ligands includes advanced glycation end products (AGEs), amyloid fibrils, amphoterin and S100/calgranulins. This variety of ligands allows RAGE to be implicated in a wide spectrum of pathological conditions such as diabetes and its complications, Alzheimer's disease, cancer and inflammation. Additionally, genetic polymorphisms in the RAGE gene may have impact on the functional activity of the receptor. It becomes obvious that RAGE pathway is a complicated one and the question of whether blockade of RAGE is a feasible and safe strategy for the prevention/treatment of chronic diseases is gradually gaining the attention of the pharmaceutical community. In this review the biology of RAGE and the triggered signaling cascades involved in health and disease will be presented. Additionally, its potential as an attractive pharmacotherapeutic target will be explored by pointing out the pharmacotherapeutic agents that have been developed for RAGE blockade.

摘要

晚期糖基化终产物受体(RAGE)表达于多种细胞类型,如内皮细胞、平滑肌细胞、系膜细胞、单核吞噬细胞和某些神经元。它是一种多配体受体,属于细胞表面分子免疫球蛋白超家族的成员。其配体包括晚期糖基化终产物(AGEs)、淀粉样纤维、两性蛋白和 S100/钙粒蛋白。这种多样化的配体使 RAGE 参与了广泛的病理状态,如糖尿病及其并发症、阿尔茨海默病、癌症和炎症。此外,RAGE 基因的遗传多态性可能对受体的功能活性有影响。很明显,RAGE 途径是一个复杂的途径,阻断 RAGE 是否是预防/治疗慢性疾病的可行和安全策略的问题逐渐引起了制药界的关注。在这篇综述中,将介绍 RAGE 的生物学以及与健康和疾病相关的触发信号级联反应。此外,通过指出已经开发用于 RAGE 阻断的药物治疗剂,探讨其作为有吸引力的药物治疗靶点的潜力。

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