RETRACTED: MicroRNA-222 promotes tumorigenesis via targeting DKK2 and activating the Wnt/β-catenin signaling pathway (Retracted Article)

被引:32
作者
Li, Qifeng [1 ]
Shen, Ke [2 ,3 ]
Zhao, Yang [1 ]
He, Xiaoguang [1 ]
Ma, Chenkai [1 ]
Wang, Lin [1 ]
Wang, Baocheng [1 ]
Liu, Jianwen [2 ,3 ]
Ma, Jie [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Xinhua Hosp, Dept Pediat Neurosurg, Shanghai 200092, Peoples R China
[2] E China Univ Sci & Technol, Sch Pharm, State Key Lab Bioreactor Engn, Shanghai 200237, Peoples R China
[3] E China Univ Sci & Technol, Sch Pharm, Shanghai Key Lab Chem Biol, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金;
关键词
miR-222; DKK2; Wnt/beta-catenin signaling pathway; Glioma; PROSTATE CARCINOMA; MALIGNANT GLIOMAS; MIR-222; PROLIFERATION; PROGRESSION; EXPRESSION; INDUCE;
D O I
10.1016/j.febslet.2013.04.002
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
MiR-222 in glioma can regulate cell cycle progression and apoptosis. However, the relationship between miR-222 and Wnt/beta-catenin signaling pathway in glioma remains unknown. Here, we found that the Dickkopf-2 gene (DKK2) was a direct target of miR-222 by target prediction analysis and dual luciferase reporter assay. RNA interference silencing of DKK2 proved that miR-222 overexpression led to constitutive activation of beta-catenin through inhibition of DKK2 expression in glioma cells. Furthermore, miR-222 siRNA significantly inhibited tumorigenesis in vivo. Finally, Western blot analysis showed that miR-222 could regulate the expression of beta-catenin and the downstream genes of Wnt/beta-catenin signaling pathway. Taken together, our findings reveal a new regulatory mechanism of miR-222 and suggest that miR-222 might be a potential target in glioma therapy. (C) 2013 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1742 / 1748
页数:7
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