Jing Rong-Rong, Cui Ming, Sun Bao-Lan, Yu Juan, Wang Hui-Min
Center of Laboratory Medicine, Affiliated Hospital of Nantong University, Nantong, Jiangsu, People's Republic of China.
Genet Test Mol Biomarkers. 2010 Jun;14(3):355-61. doi: 10.1089/gtmb.2009.0064.
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.
晚期糖基化终末产物受体(RAGE)与多种配体相互作用,并参与多种人类疾病。RAGE基因的几种剪接形式已得到表征,通常有两种一般机制负责可溶性受体的产生。然而,不同肿瘤中的变体分布及其各自的作用尚不清楚。我们通过逆转录聚合酶链反应分析了食管癌和肺癌中RAGE和hRAGEsec mRNA的表达。使用芯片实验室技术的安捷伦Clipper 1000生物分析仪用于对聚合酶链反应产物进行大小分析和定量。进行蛋白质免疫印迹以测量总可溶性RAGE蛋白水平。结果表明,RAGE及其剪接变体在食管癌中增加,在肺癌中减少。我们得出结论,RAGE以主要异构体形式存在;可溶性RAGE在食管癌和肺癌中可能也发挥一定作用。