MicroRNA-7 inhibits metastasis and invasion through targeting focal adhesion kinase in cervical cancer

被引:0
|
作者
Hao, Zhenfeng [1 ]
Yang, Jishi [1 ]
Wang, Chenghai [2 ]
Li, Yaoyao [3 ]
Zhang, Yu [3 ]
Dong, Xiaoyun [3 ]
Zhou, Liulin [1 ]
Liu, Jing [1 ]
Zhang, Yanqing [2 ]
Qian, Jing [3 ]
机构
[1] Yangzhou Univ, Taixing Peoples Hosp, Dept Obstet & Gynecol, Taizhou 225004, Jiangshu, Peoples R China
[2] Yangzhou Univ, Coll Med, Dept Pathol, Yangzhou 225001, Jiangsu, Peoples R China
[3] Yangzhou Univ, Jiangsu Key Lab Intergrated Tradit Chinese & West, Yangzhou 225001, Jiangsu, Peoples R China
来源
INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE | 2015年 / 8卷 / 01期
基金
美国国家科学基金会;
关键词
microRNA; miR-7; focal adhesion kinase; cervical cancer; metastasis; invasion; EXPRESSION; CELLS; FAK; GROWTH; MIR-7; MIRNAS; EGFR;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
MicroRNAs (miRNAs) are aberrantly expressed in cervical cancer. miR-7 has been demonstrated to function as both an oncogene and a tumor suppressor in some types of human cancers. In the present study, miR-7 was significantly downregulated in cervical cancer, especially metastatic tumors. Ectopic expression of miR-7 significantly inhibited metastasis and invasion in Hela and C33A cells. Upregulated miR-7 significantly suppressed focal adhesion kinase (FAK) at transcriptional and translational levels. Furthermore, the level of FAK was negatively correlated with miR-7 in cervical cancer tissues. In conclusion, miR-7 inhibited the metastasis and invasion of cervical cancer at least partially through targeting FAK. The findings of this study provide novel insight with potential therapeutic applications for the treatment of metastatic cervical cancer.
引用
收藏
页码:480 / 487
页数:8
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