Tissue-Specific Expression Profiling of Receptor for Advanced Glycation End Products and Its Soluble Forms in Esophageal and Lung Cancer

被引:22
作者
Jing, Rong-Rong [1 ]
Cui, Ming [1 ]
Sun, Bao-Lan [1 ]
Yu, Juan [1 ]
Wang, Hui-Min [1 ]
机构
[1] Nantong Univ, Affiliated Hosp, Ctr Lab Med, Nantong 226001, Jiangsu, Peoples R China
关键词
CELL-SURFACE RECEPTOR; RAGE RECEPTOR; AMPHOTERIN; COEXPRESSION; ENDPRODUCTS; MEDIATOR; BINDING; CLONING; GROWTH; ROLES;
D O I
10.1089/gtmb.2009.0064
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) interacts with several ligands and is involved in various human diseases. Several splicing forms of the RAGE gene have been characterized, and two general mechanisms are usually responsible for the generation of soluble receptors. However, variants distribution and respective roles in different tumors are not clear. We analyzed RAGE and hRAGEsec mRNA expression in esophageal and lung cancer by RT-polymerase chain reaction. The Agilent clipper 1000 Bioanalyzer using lab-on-a- chip technology was applied to size and quantify the polymerase chain reaction products. Western blotting was performed to measure total soluble RAGE protein levels. The results showed that RAGE and its splice variants increased in esophageal cancers and decreased in lung cancers. We conclude that RAGE presents as a major isoform; soluble RAGE may also play certain roles in esophageal cancer and lung cancer.
引用
收藏
页码:355 / 361
页数:7
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