Retroviral IFN-alpha gene transfer combined with gemcitabine acts synergistically via cell cycle alteration in human pancreatic carcinoma cells implanted orthotopically in nude mice

J Interferon Cytokine Res. 2004 Aug;24(8):490-6. doi: 10.1089/1079990041689647.

Abstract

Standard chemotherapy for pancreatic carcinoma is based on the use of gemcitabine. The clinical benefit of interferon-alpha (IFN-alpha) in advanced pancreatic cancer has been shown. However, it has been demonstrated that to be effective, there is a need for a constant amount of IFN-alpha at the site of the tumor. Therefore, we examined transfection of the human pancreatic cancer cell line DAN-G with a retrovirus encoding for IFN-alpha and the effect of IFN-alpha gene expression alone or in combination with gemcitabine on growth inhibition of DAN-G pancreatic cancer cells in vitro and in vivo in orthotopically implanted DAN-G cells in nude mice. DAN-G cells could be efficiently transfected retrovirally by the human IFN-alpha gene and significantly enhanced the levels of IFN-alpha mRNA. In vitro gemcitabine led to an alteration of G1/S phase progression in transduced as well as untransduced cells, whereas IFN-alpha led to a significant decrease in cell viability in the transduced cells via delay in the progression of the S phase but no alteration of G1/S phase progression. In vivo, tumor volume in mice was reduced significantly with gemcitabine combined with IFN-alpha (76% +/- 8.3%) compared with gemcitabine alone (62.9% +/- 7.3%) or IFN-alpha alone (24.4% +/- 5.2%) compared with untreated animals. We conclude that gemcitabine and IFN-alpha concomitantly inhibited tumor cell proliferation significantly.

MeSH terms

  • Animals
  • Antineoplastic Agents / pharmacology
  • Cell Cycle* / drug effects
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • DNA, Complementary / genetics
  • Deoxycytidine / analogs & derivatives*
  • Deoxycytidine / pharmacology*
  • Deoxycytidine / therapeutic use
  • Female
  • Gemcitabine
  • Gene Expression
  • Genetic Therapy
  • Humans
  • Interferon-alpha / biosynthesis
  • Interferon-alpha / genetics*
  • Interferon-alpha / metabolism
  • Mice
  • Mice, Nude
  • Neoplasm Metastasis / genetics
  • Neoplasm Metastasis / pathology
  • Neoplasm Transplantation
  • Pancreatic Neoplasms / genetics*
  • Pancreatic Neoplasms / metabolism
  • Pancreatic Neoplasms / pathology*
  • Pancreatic Neoplasms / therapy
  • Retroviridae / genetics*
  • Transgenes / genetics

Substances

  • Antineoplastic Agents
  • DNA, Complementary
  • Interferon-alpha
  • Deoxycytidine
  • Gemcitabine