miR-1271 inhibits growth, invasion and epithelial-mesenchymal transition by targeting ZEB1 in ovarian cancer cells

被引:14
|
作者
Jiao, Yanni [1 ]
Zhu, Guiping [1 ]
Yu, Jiang [1 ]
Li, Ying [1 ]
Wu, Man [2 ]
Zhao, Jing [1 ]
Tian, Xiangwen [1 ]
机构
[1] Shengli Oil Field, Dept Obstet & Gynecol, Cent Hosp, 31 Jinan Rd, Dongying 257000, Peoples R China
[2] Shengli Oil Field, Dept Pediat, Cent Hosp, Dongying 257000, Peoples R China
来源
ONCOTARGETS AND THERAPY | 2019年 / 12卷
关键词
miR-1271; proliferation; invasion; epithelial-mesenchymal transition (EMT); ovarian cancer; PROMOTES APOPTOSIS; GASTRIC-CANCER; PROLIFERATION; MIGRATION; MICRORNA-1271; EXPRESSION; TWIST1;
D O I
10.2147/OTT.S219018
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
Objective: MicroRNA-1271 (miR-1271) has a role in suppressing cell growth, cell cycle and promoting cell apoptosis in many cancers. This research was to explore the great role of miR-1271 in ovarian cancer (OC). Patients and Methods: RT-qPCR was utilized to evaluate the mRNA levels of miR-1271 and its target gene. The proliferative and invasive abilities were measured using Cell Counting Kit-8 and transwell assays. The overall survival rate of OC patients was assessed by Kaplan-Meier method. Results: miR-1271 was downregulated in OC tissues, and downregulation of miR-1271 predicted a poor outcome of the OC patients. Zinc finger E-box binding homeobox 1 (ZEB1) was a target gene of miR-1271 and its expression was regulated by miR-1271 in OC. The expression of miR-1271 had a negative connection with the expression of ZEB1 in OC tissues. miR-1271 inhibited cell viability and invasion-mediated epithelial-mesenchymal transition in SKOV3 cells. ZEB1 reversed partial roles of miR-1271 on viability and invasion in OC. Conclusion: miR-1271 inhibited cell proliferation and invasion-mediated EMT in OC. The newly identified miR-1271/ZEB1 axis provides novel insight into the pathogenesis of OC.
引用
收藏
页码:6973 / 6980
页数:8
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