Tissue specific cytotoxicity of colon cancer cells mediated by nanoparticle-delivered suicide gene in vitro and in vivo

Clin Cancer Res. 2009 Jan 1;15(1):201-7. doi: 10.1158/1078-0432.CCR-08-1094.

Abstract

Purpose: This study aimed to develop an efficient and safe strategy to introduce suicide genes into colon cancer cells.

Experimental design: In this study, we fused an enhanced carcinoembryonic antigen promoter (CEA) to a suicide gene, cytosine deaminase (CD). This construct was delivered into colon cancer cells using calcium phosphate nanoparticles (CPNP). The cells were then treated with the prodrug 5-FC. The therapeutic effect was evaluated in vitro and in vivo.

Results: Our study showed that the CEA promoter-driven, CPNP-delivered suicide gene was only expressed in CEA-positive colon cancer cells, and resulted in significant cytotoxicity after administration of the prodrug 5-FC in vitro. Moreover, our in vivo study showed that CPNP-mediated CEA-CD delivery, together with 5-FC treatment, resulted in significant tumor growth delay in xenograft human colon carcinoma.

Conclusions: Our study indicates that the combination of CPNP and CEA-CD gene expression represents a novel approach for CEA-positive tumor gene therapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis
  • Calcium Phosphates
  • Carcinoembryonic Antigen / genetics
  • Cell Line, Tumor
  • Colonic Neoplasms
  • Cytosine Deaminase / genetics*
  • Fluorouracil / therapeutic use
  • Genes, Transgenic, Suicide*
  • Genetic Therapy / methods*
  • Genetic Vectors
  • Humans
  • Mice
  • Mice, Nude
  • Nanoparticles*
  • Promoter Regions, Genetic
  • Xenograft Model Antitumor Assays

Substances

  • Calcium Phosphates
  • Carcinoembryonic Antigen
  • calcium phosphate
  • Cytosine Deaminase
  • Fluorouracil