E2F promoter-regulated oncolytic adenovirus with p16 gene induces cell apoptosis and exerts antitumor effect on gastric cancer

Dig Dis Sci. 2009 Jul;54(7):1425-31. doi: 10.1007/s10620-008-0543-0. Epub 2008 Nov 26.

Abstract

Replication-competent adenovirus (RCAd) constitutes an alternative in cancer therapy. For obtaining advanced RCAd generations with high oncolytic capability and a good safety profile, we constructed an E2F promoter-regulated RCAd carrying p16 gene, AdE2F-p16, in which the E1a gene was controlled by the E2F promoter. The experimental data showed that the E2F promoter endowed AdE2F-p16 with high specificity in cancer cells. While rarely replicating in normal cells, AdE2F-p16 could replicate in p16-deficient cancer cells, with 2,937- to 160,000-fold increased replicative capability in different cancer cell lines. AdE2F-p16 expressed p16 within cancer cells and led to potent antitumor efficacy in gastric cancer xenografts in nude mice, with a tumor inhibition rate of 59.14%. Due to the combined effects of cancer cell apoptosis induced by p16 expression and oncolysis by virus replication, the E2F promoter-regulated, p16-armed RCAd provides a promising strategy for cancer gene therapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenoviridae / physiology
  • Animals
  • Apoptosis / genetics
  • Cell Cycle / physiology
  • Cell Line, Tumor
  • DNA-Binding Proteins
  • E2F Transcription Factors / physiology*
  • Gene Expression Regulation, Neoplastic / physiology
  • Genes, p16 / physiology*
  • Genetic Vectors
  • Humans
  • Luciferases / metabolism
  • Mice
  • Mice, Inbred BALB C
  • Oncolytic Virotherapy / methods*
  • Signal Transduction / physiology
  • Stomach Neoplasms / genetics*
  • Stomach Neoplasms / virology
  • Virus Replication / genetics*
  • Xenograft Model Antitumor Assays

Substances

  • DNA-Binding Proteins
  • E2F Transcription Factors
  • Luciferases