miR-148a promoted cell proliferation by targeting p27 in gastric cancer cells

Int J Biol Sci. 2011 May 5;7(5):567-74. doi: 10.7150/ijbs.7.567.

Abstract

Accumulating evidence has shown that miRNAs are aberrantly expressed in human gastric cancer and crucial to tumorigenesis. Herein, we identified the role of miR-148a in gastric cell proliferation. miR-148a knockdown inhibited cell proliferation in gastric cancer cell lines. Conversely, miR-148a overexpression promoted cell proliferation and cell cycle progression. p27, a key inhibitor of cell cycle, was verified as the target of miR-148a, indicating miR-148a might downregulate p27 expression to promote gastric cell proliferation. Moreover, we confirmed that miR-148a expression was frequently and dramatically downregulated in human advanced gastric cancer tissues, and observed a good inverse correlation between miR-148a and p27 expression in tumor samples. Thus, our results demonstrated that miR-148a downregulation might exert some sort of antagonistic function in cell proliferation, rather than promote cell proliferation in gastric cancer.

Keywords: cell proliferation; gastric cancer; miR-148a; p27.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Cell Proliferation*
  • Cyclin-Dependent Kinase Inhibitor p27 / metabolism*
  • Down-Regulation
  • Humans
  • Mice
  • MicroRNAs / metabolism*
  • Stomach Neoplasms / metabolism*

Substances

  • MIRN148 microRNA, human
  • MicroRNAs
  • Cyclin-Dependent Kinase Inhibitor p27