Down-regulated miRNA-214 induces a cell cycle G1 arrest in gastric cancer cells by up-regulating the PTEN protein

Pathol Oncol Res. 2011 Dec;17(4):931-7. doi: 10.1007/s12253-011-9406-7. Epub 2011 Jun 19.

Abstract

To detect the expression of miRNA-214 in human gastric cancer cell lines of BGC823, MKN45 and SGC7901, and to identify the effect of miRNA-214 on cell cycle and apoptosis of these cells. Expression of miRNA-214 in human normal gastric mucosal cell line GES-1 and human gastric cancer cell lines was detected by real-time reverse-transcription polymerase chain reaction. Antisense-miRNA-214 oligonucleotides were transfected transiently into gastric cancer cell lines to down-regulate the expression of miRNA-214. The cell cycle and apoptosis were studied by flow cytometry assay. PTEN, one of the target genes of miRNA-214 was detected by using of immunocytochemistry and Western blotting. MiRNA-214 was overexpressed in gastric cancer cell lines of BGC823, MKN45 and SGC7901 compared with normal gastric mucosal cell line GES-1. Antisense-miRNA-214 oligonucleotides significantly down-regulated the expression of miRNA-214, and increased the portion of G1-phase and decreased the portion of S-phase in BGC823 and MKN45 cells. The immunocytochemistry test and Western blotting analysis showed that the down-regulation of miRNA-214 could significantly up-regulate the expression of PTEN in BGC823 and MKN45 cells. MiRNA-214 is overexpressed in human gastric cancer cell lines of BGC823, MKN45 and SGC7901. The down-regulation of miRNA-214 could induce a G1 cell cycle arrest in them, the up-regulation of PTEN maybe one of the mechanism.

MeSH terms

  • Apoptosis / genetics
  • Blotting, Western
  • Cell Cycle Checkpoints / genetics*
  • Cell Line
  • Cell Line, Tumor
  • Down-Regulation
  • G1 Phase / genetics*
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • MicroRNAs / biosynthesis
  • MicroRNAs / genetics*
  • Oligonucleotides, Antisense / genetics
  • PTEN Phosphohydrolase / biosynthesis
  • PTEN Phosphohydrolase / genetics*
  • Real-Time Polymerase Chain Reaction / methods
  • S Phase / genetics
  • Stomach Neoplasms / genetics*
  • Stomach Neoplasms / metabolism
  • Transfection
  • Up-Regulation

Substances

  • MicroRNAs
  • Oligonucleotides, Antisense
  • PTEN Phosphohydrolase
  • PTEN protein, human