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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.
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页码:455 / 461
页数:7
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