miR-29a suppresses growth and invasion of gastric cancer cells in vitro by targeting VEGF-A

被引:62
作者
Chen, Ling [1 ]
Xiao, Hong [1 ]
Wang, Zong-Hua [2 ]
Huang, Yi [1 ]
Liu, Zi-Peng [1 ]
Ren, Hui [2 ]
Song, Hang [1 ]
机构
[1] PLA, Hosp 324, Dept Gastroenterol, Chongqing 400020, Peoples R China
[2] Third Mil Med Univ, Sch Nursing, Chongqing 400038, Peoples R China
关键词
Gastric cancer; Hsa-miR-29a; MicroRNAs; Post-transcriptional regulation; VEGF-A; MICROVESSEL DENSITY; MICRORNA-21; TARGETS; GENE-EXPRESSION; DOWN-REGULATION; TUMOR; PROLIFERATION; PREDICTION;
D O I
10.5483/BMBRep.2014.47.1.079
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Increasing data shows miR-29a is a key regulator of oncogenic processes. It is significantly down-regulated in some kind of human tumors and possibly functionally linked to cellular proliferation, survival and migration. However, the mechanism remains unclear. In this study, we report miR-29a is significantly under-expressed in gastric cancer compared to the healthy donor. The microvessel density is negatively related to miR-29a expression in gastric cancer tissues. The ectopic expression of miR-29a significantly inhibits proliferation and invasion of gastric cancer cells. Furthermore, western blot combined with the luciferase reporter assays demonstrate that vascular endothelial growth factor A (VEGF-A) is direct target of miR-29a. This is the first time miR-29a was found to suppress the tumor microvessel density in gastric cancer by targeting VEGF-A. Taken together, these results suggest that miR-29a is a tumor suppressor in gastric cancer. Restoration of miR-29a in gastric cancer may be a promising therapeutic approach.
引用
收藏
页码:39 / 44
页数:6
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