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Induction of growth arrest by miR-542-3p that targets survivin.

Abstract
Survivin is a protein which functions as a mitotic regulator as well as apoptosis inhibitor. In this study, we show that introduction of synthetic miR-542-3p mimetic reduced both mRNA and protein levels of survivin. In A549 cells, luciferase reporter assay revealed that miR-542-3p targeted predicted binding sites in the 3'-untranslated region (3'-UTR) of survivin. We also demonstrate that ectopic expression of miR-542-3p inhibited cell proliferation by inducing Gap 1 (G1) and Gap 2/Mitosis (G2/M) cell cycle arrest. Collectively, these results suggest that survivin is a direct target of miR-542-3p and growth inhibition by miR-542-3p may have a potential utility as an anti-cancer therapy.
AuthorsSena Yoon, Young-Chul Choi, Suman Lee, Yongsu Jeong, Jaeseung Yoon, Kwanghee Baek
JournalFEBS letters (FEBS Lett) Vol. 584 Issue 18 Pg. 4048-52 (Sep 24 2010) ISSN: 1873-3468 [Electronic] England
PMID20728447 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2010 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
Chemical References
  • BIRC5 protein, human
  • Inhibitor of Apoptosis Proteins
  • MicroRNAs
  • Microtubule-Associated Proteins
  • Survivin
Topics
  • Cell Cycle (genetics)
  • Cell Line, Tumor
  • Cell Proliferation
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Inhibitor of Apoptosis Proteins
  • MicroRNAs (genetics, metabolism)
  • Microtubule-Associated Proteins (genetics)
  • Mitosis (genetics)
  • Oligonucleotide Array Sequence Analysis
  • Survivin

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