4.5 Article

MicroRNA-222 promotes tumorigenesis via targeting DKK2 and activating the Wnt/β-catenin signaling pathway

期刊

FEBS LETTERS
卷 587, 期 12, 页码 1742-1748

出版社

WILEY
DOI: 10.1016/j.febslet.2013.04.002

关键词

miR-222; DKK2; Wnt/beta-catenin signaling pathway; Glioma

资金

  1. National Key Basic Research Program (NKBRP) [2010CB945203]
  2. National Natural Science Foundation of China [81271382]
  3. Program Of Shanghai Subject Chief Scientist [09XD1403300]
  4. Shanghai Jiaotong University School of Medicine [BXJ201223]

向作者/读者索取更多资源

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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