Effect of S1P5 on proliferation and migration of human esophageal cancer cells  被引量:8

Effect of S1P5 on proliferation and migration of human esophageal cancer cells

在线阅读下载全文

作  者:Hu, Wei-Min Li, Li Ing, Bao-Qian Zhao, Yong-Sheng Wang, Chao-Li Feng, Li Xie, Yong-En 

机构地区:[1]N Sichuan Med Coll, Dept Microbiol & Immunol, Nanchong 637007, Sichuan Prov, Peoples R China [2]N Sichuan Med Coll, Inst Immunol & Mol Biol, Nanchong 637007, Sichuan Prov, Peoples R China [3]N Sichuan Med Coll, Affiliated Hosp, Dept Thorac Surg, Nanchong 637007, Sichuan Prov, Peoples R China

出  处:《World Journal of Gastroenterology》2010年第15期1859-1866,共8页世界胃肠病学杂志(英文版)

基  金:Supported by The Key Project of Ministry of Education, No. 209105;Sichuan Youth Science and Technology Foundation, No. 08ZQ026-081;Key Laboratory Foundation of North Sichuan Medical College, No. KFJJ (08)-03

摘  要:AIM:To investigate the sphingosine 1phosphate (S1P) receptor expression profile in human esophageal cancer cells and the effects of S1P5 on proliferation and migration of human esophageal cancer cells. METHODS: S1P receptor expression profile in human esophageal squamous cell carcinoma cell line Eca109 was detected by semiquantitative reverse trans cription polymerase chain reaction. Eca109 cells were stably transfected with S1P5EGFP or controlEGFP constructs. The relation between the responses of cell proliferationand migration to S1P and S1P5 expres sion was evaluated by 3(4,5dimethylthiazol2yl)2,5diphenyl tetrazolium bromide and migration assay, respectively. RESULTS: Both normal human esophageal mucosal epithelium and Eca109 cells expressed S1P1, S1P2, S1P3 and S1P5, respectively. Esophageal mucosal epithelium expressed S1P5 at a higher level than Eca109 cell line. S1P5 overexpressing Eca109 cells displayed spindle cell morphology with elongated and extended filopodialike projections. The proliferation response of S1P5transfected Eca109 cells was lower than that of control vectortransfected cells with or without S1P stimulation (P < 0.05 or 0.01). S1P significantly inhibited the migration of S1P5transfected Eca109 cells (P < 0.001). However, without S1P in transwell lower chamber, the number of migrated S1P5transfected Eca109 cells was greater than that of control vectortransfected Eca109 cells (P < 0.001).CONCLUSION: S1P binding to S1P5 inhibits the proliferation and migration of S1P5transfected Eca109 cells. Esophageal cancer cells may downregulate the expression of S1P5 to escape the inhibitory effect.AIM:To investigate the sphingosine 1phosphate (S1P) receptor expression profile in human esophageal cancer cells and the effects of S1P5 on proliferation and migration of human esophageal cancer cells. METHODS: S1P receptor expression profile in human esophageal squamous cell carcinoma cell line Eca109 was detected by semiquantitative reverse trans cription polymerase chain reaction. Eca109 cells were stably transfected with S1P5EGFP or controlEGFP constructs. The relation between the responses of cell prol...

关 键 词:Sphingosine 1phosphate Esophageal cancer Sphingosine 1phosphate 5 PROLIFERATION MIGRATION 

分 类 号:R735.1[医药卫生—肿瘤]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象