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RETRACTED: MicroRNA-222 promotes tumorigenesis via targeting DKK2 and activating the Wnt/β-catenin signaling pathway (Retracted Article)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.
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页码:1742 / 1748
页数:7
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