Angiopoietin-1 targeted RNA interference suppresses angiogenesis and tumor growth of esophageal cancer

被引:9
作者
Liu, Xiao-Hong [1 ]
Bai, Chen-Guang [2 ]
Yuan, Yang [1 ]
Gong, De-Jun [1 ]
Huang, Sheng-Dong [1 ]
机构
[1] Second Mil Med Univ, Changhai Hosp, Inst Thoracardiac Surg, Shanghai 200433, Peoples R China
[2] Second Mil Med Univ, Changhai Hosp, Dept Pathol, Shanghai 200433, Peoples R China
关键词
angiopoietin-1; angiogenesis; esophageal cancer; RNA interference; cancer;
D O I
10.3748/wjg.14.1575
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To determine the inhibitory effect of the adenovirus-based angiopoietin-1 (Ang-1) targeted small interfering RNA expression system (Ad/Ang-1si) on the expression of the Ang-1 gene, cell growth and apoptosis in human esophageal cancer cell line Eca109. METHODS: siRNA-expressing adenovirus targeting Ang-1 gene was constructed using the Ad Easy System. Cultured Eca109 cells were transfected with Ad/Ang-1si (Eca109/Ang-1si), and Ad/si was used to infect Eca109 cells as control (Eca109/si). Ang-1 gene expression and concentration was determined with RT-PCR and ELISA, respectively. Human umbilical vein endothelial cell (HUVEC) migration and proliferation were analyzed. After s.c. injection into athymic nu/nu mice, the tumor growth, vessel density and apoptosis of each group was also determined. RESULTS: HUVEC migration induced by conditioned medium from Ang-1si-transfected Eca109 cells was significantly less than that induced by conditioned medium from Eca109 cells and control adenovirus-transfected Eca109 cells. Furthermore, after s.c. injection into athymic nu/nu mice, the tumor growth and cell apoptosis of Ad/Ang-1si -expressing Eca109 cells was significantly lower than that of parental or control adenovirus-transfected cells. Vessel density assessed by CD31 immunohistochemical analysis and Ang-1 expression by RT-PCR were also decreased. CONCLUSION: The targeting Ang-1 may provide a therapeutic option for esophageal cancer. (C) 2008 WJG. All rights reserved.
引用
收藏
页码:1575 / 1581
页数:7
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