Alternative splicing of RAGE: roles in biology and disease

被引:70
作者
Kalea, Anastasia Z. [2 ]
Schmidt, Ann Marie [3 ]
Hudson, Barry I. [1 ]
机构
[1] Univ Miami, Miller Sch Med, Div Endocrinol Diabet & Metab, Miami, FL 33136 USA
[2] Northwestern Univ, Feinberg Sch Med, Div Nephrol Hypertens, Evanston, IL 60208 USA
[3] NYU, Langone Med Ctr, Dept Med & Pharmacol, New York, NY 10003 USA
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2011年 / 16卷
关键词
Alternative splicing; receptors; Advanced Glycation End-products; mRNA; Review; GLYCATION END-PRODUCTS; ENDOGENOUS SECRETORY RAGE; COMMUNITY-DWELLING WOMEN; CORONARY-ARTERY-DISEASE; NUCLEAR RIBONUCLEOPROTEIN H; TYPE-1; DIABETIC-PATIENTS; DECREASED PLASMA-LEVELS; CELL-SURFACE RECEPTOR; E-NULL MICE; SOLUBLE RECEPTOR;
D O I
10.2741/3884
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Receptor for Advanced Glycation End-products (RAGE) is a complex, multi-ligand signaling system implicated in the pathogenesis of diabetes, cardiovascular disease and various cancers. RAGE undergoes extensive alternative splicing to produce a variety of transcripts with diverse functions, including soluble antagonists and variants with altered ligand binding domains. Studies focused on the major soluble variant (RAGEv1/esRAGE) have revealed this to function by binding RAGE-ligands and preventing activation of RAGE signaling in vascular and tumor cells. Furthermore, measurement of this variant in human serum has revealed that RAGEv1/esRAGE levels may represent a novel biomarker for RAGE-ligand related pathogenic states. Understanding the full plethora of RAGE alternative splicing and its regulation is central to elucidating the role of RAGE in biology and disease.
引用
收藏
页码:2756 / 2770
页数:14
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