miR-25-3p inhibition impairs tumorigenesis and invasion in gastric cancer cells in vitro and in vivo

被引:37
|
作者
Ning, Liang [1 ]
Zhang, Maoshen [1 ]
Zhu, Qingli [2 ]
Hao, Fengyun [3 ]
Shen, Wenlong [4 ]
Chen, Dong [1 ]
机构
[1] Qingdao Univ, Affiliated Hosp, Dept Gen Surg, Qingdao 266003, Shandong, Peoples R China
[2] Qingdao Univ, Affiliated Hosp, Dept Thyroid Surg, Qingdao, Shandong, Peoples R China
[3] Qingdao Univ, Affiliated Hosp, Dept Pathol, Qingdao, Shandong, Peoples R China
[4] Shandong Univ, Qilu Hosp, Dept Anorectal, Qingdao, Shandong, Peoples R China
关键词
Gastric cancer; miR-25-3p; miR-25; inhibitor; Metastasis; Invasion; microRNA; PROLIFERATION; PROGRESSION; MIGRATION; BOX;
D O I
10.1080/21655979.2019.1710924
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Deregulated expression of microRNAs (miRNAs) plays a role in the pathogenesis and progression of gastric cancer (GC). Among upregulated miRNAs, miR-25-3p has oncogenic potential and therefore represents an attractive target for the treatment of GC. Here, we investigated the role of miR-25-3p on GC cells in vitro and in vivo. We found that miR-25-3p overexpression significantly promoted growth and invasion of gastric cancer cells in vitro. Conversely, targeting miR-25-3p triggered significant inhibition of growth, invasion and migration in GC cells in vitro. In vivo delivery of miR-25-3p inhibitors induced significant anti-tumor activity in SCID mice bearing human GC xenografts. Our findings showed the evidence that in vivo antagonism of miR-25-3p impaired tumorigenesis, providing the rationale for clinical development of miR-25-3p inhibitors in GC.
引用
收藏
页码:81 / 90
页数:10
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