miR-342-3p suppresses proliferation, migration and invasion by targeting FOXM1 in human cervical cancer

被引:106
|
作者
Li, Xu-ri [1 ,2 ]
Chu, Hui-jun [1 ]
Lv, Teng [1 ]
Wang, Lei [1 ]
Kong, Shou-fang [1 ,2 ]
Dai, Shu-zhen [1 ,3 ,4 ]
机构
[1] Qingdao Univ, Affiliated Hosp, Dept Obstet & Gynecol, Qingdao 266003, Peoples R China
[2] Qingdao Univ Med Coll, Affiliated Hiser Med Grp, Dept Gynecol & Obstet, Qingdao, Peoples R China
[3] Gynecol Tumors & Reprod Funct Protect Lab Qingdao, Qingdao, Peoples R China
[4] Key Lab Cerv Dis Qingdao, Qingdao, Peoples R China
来源
FEBS LETTERS | 2014年 / 588卷 / 17期
关键词
miR-342-3p; EVL; Forkhead Box M1; Cervical cancer; M1 TRANSCRIPTION FACTOR; COLORECTAL-CANCER; CELL-PROLIFERATION; EXPRESSION; THERAPY; ANGIOGENESIS; GENES; EVL;
D O I
10.1016/j.febslet.2014.07.020
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
FOXM1 is a well-established oncogenic factor that has been reported to be involved in multiple biological processes including cell proliferation, growth, angiogenesis, migration and invasion. It can also be regulated by miRNAs. In this study, we reported that FOXM1 is directly targeted by miR-342-3p, which is down-regulated along with its host gene, EVL, in human cervical cancer tissues compared to the adjacent normal tissues. Functional studies suggested that the overexpression of miR-342-3p inhibits cell proliferation, migration and invasion in cervical cell lines. FOXM1 is upregulated and negatively correlates with miR-342-3p in cervical cancer tissues, and the overexpression of FOXM1 rescues the phenotype changes induced by the overexpression of miR-342-3p. (C) 2014 Published by Elsevier B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:3298 / 3307
页数:10
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