miR-342-3p suppresses proliferation, migration and invasion by targeting FOXM1 in human cervical cancer.
By: Xu-Ri Li, Hui-Jun Chu, Teng Lv, Lei Wang, Shou-Fang Kong, Shu-Zhen Dai

Department of Obstetrics and Gynecology, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, China; Department of Gynecology and Obstetrics, The Affiliated Hiser Medical Group of Qingdao University Medical College, Qingdao, China.
2014-6-18; doi: 10.1016/j.febslet.2014.07.020
Abstract

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.



Copyright © 2014. Published by Elsevier B.V.

PMID:25066298






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