Suppression of gastric cancer growth by baculovirus vector-mediated transfer of normal epithelial cell specific-1 gene

World J Gastroenterol. 2008 Oct 14;14(38):5810-5. doi: 10.3748/wjg.14.5810.

Abstract

Aim: To study the inhibitory effect of baculovirus-mediated normal epithelial cell specific-1 (NES1) gene therapy on gastric cancer (GC) in vitro and in vivo.

Methods: We first constructed recombinant baculovirus vectors and then transfected them into gastric cancer cells (SGC-7901). Efficiency of the baculovirus for gene transfer into SGC-7901 cells and cell growth curves were detected by fluorescence microscopy, Western blot and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay in vitro, respectively. The therapeutic effect of this gene therapy on GC was confirmed in xenografted nude mice. Tumor growth was determined by tumor volume, and expression of NES1 in tumor was analyzed by immunohistochemistry.

Results: Baculovirus vectors were successfully transfected into SGC-7901 cells. SGC-7901 cells transfected with the NES1 gene inhibited cell growth. In the Bac-NES1 treated group, tumor growth was significantly reduced with a high level of NES1 expression

Conclusion: Baculovirus-mediated NES1 gene can be used in gene therapy for GC.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Baculoviridae / genetics*
  • Cell Line, Tumor
  • Cell Proliferation*
  • Genes, Reporter
  • Genetic Therapy / methods*
  • Genetic Vectors*
  • Green Fluorescent Proteins / genetics
  • Humans
  • Kallikreins / genetics*
  • Kallikreins / metabolism
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Stomach Neoplasms / genetics
  • Stomach Neoplasms / metabolism
  • Stomach Neoplasms / pathology
  • Stomach Neoplasms / therapy*
  • Time Factors
  • Transduction, Genetic
  • Transfection
  • Xenograft Model Antitumor Assays

Substances

  • Green Fluorescent Proteins
  • KLK10 protein, human
  • Kallikreins