Inhibition of PRL-3 gene expression in gastric cancer cell line SGC7901 via microRNA suppressed reduces peritoneal metastasis

Biochem Biophys Res Commun. 2006 Sep 15;348(1):229-37. doi: 10.1016/j.bbrc.2006.07.043. Epub 2006 Jul 18.

Abstract

High expression of PRL-3, a protein tyrosine phosphatase, is proved to be associated with lymph node metastasis in gastric carcinoma from previous studies. In this paper, we examined the relationship between PRL-3 expression and peritoneal metastasis in gastric carcinoma. We applied the artificial miRNA (pCMV-PRL3miRNA), which is based on the murine miR-155 sequence, to efficiently silence the target gene expression of PRL-3 in SGC7901 gastric cancer cells at both mRNA and protein levels. Then we observed that, in vitro, pCMV-PRL3miRNA significantly depressed the SGC7901 cell invasion and migration independent of cellular proliferation. In vivo, PRL-3 knockdown effectively suppressed the growth of peritoneal metastases and improved the prognosis in nude mice. Therefore, we concluded that artificial miRNA can depress the expression of PRL-3, and that PRL-3 might be a potential therapeutic target for gastric cancer peritoneal metastasis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Cell Movement / genetics
  • Cell Proliferation
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Immediate-Early Proteins / genetics*
  • Mice
  • MicroRNAs
  • Neoplasm Transplantation
  • Peritoneal Neoplasms / genetics
  • Peritoneal Neoplasms / secondary
  • Plasmids
  • Protein Tyrosine Phosphatases / genetics*
  • Stomach Neoplasms / genetics*
  • Stomach Neoplasms / pathology

Substances

  • Immediate-Early Proteins
  • MicroRNAs
  • Ptp4a3 protein, mouse
  • Protein Tyrosine Phosphatases