MicroRNA-509-3p Inhibits Cancer Cell Proliferation and Migration via Upregulation of XIAP in Gastric Cancer Cells

被引:29
|
作者
Sun, Jihong [1 ,2 ]
Li, Jingjing [3 ]
Zhang, Weiguo [1 ]
Zhang, Juan [1 ]
Sun, Shenjie [1 ]
Li, Guiqi [1 ]
Song, Hengliang [1 ]
Wan, Daguo [1 ]
机构
[1] Zhengzhou Univ, Affiliated Hosp 2, Dept Cardiol, Zhengzhou, Peoples R China
[2] Zhengzhou Univ, Affiliated Hosp 1, Dept Gastroenterol, Zhengzhou, Peoples R China
[3] Zhengzhou Univ, Affiliated Hosp 1, Dept Infect Dis, Zhengzhou, Peoples R China
关键词
Gastric cancer (GC); MicroRNA-509-3p (miR-509-3p); X-linked inhibitor of apoptosis protein (XIAP); GASTROESOPHAGEAL JUNCTION; STEM-CELLS; PHASE-II; APOPTOSIS; RECEPTORS; CARCINOMA; TARGET;
D O I
10.3727/096504016X14747283032017
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Gastric cancer (GC) is the fourth most common cancer globally. Recently, microRNAs (miRNAs) have been suggested to be closely associated with tumorigenesis. Aberrant expression of miR-509-3p has been reported in cancer studies. However, the expression and mechanism of its function in GC remain unclear. Here we showed that miR-509-3p was downregulated in GC specimens, which was associated with overall survival. Functional investigations demonstrated that the overexpression of miR-509-3p inhibited the migration and proliferation of the GC cells. Additionally, we identified X-linked inhibitor of apoptosis protein (XIAP) as a direct target of miR-509-3p. Knockdown of XIAP significantly attenuated the ability of proliferation, migration, and invasion of GC cells. The data therefore suggest that miR-509-3p plays an important role in the development and progression of GC, implicating possible applications in the clinic as a biomarker and a potential new target.
引用
收藏
页码:455 / 461
页数:7
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