rAAV9-UPII-TK-EGFP can precisely transduce a suicide gene and inhibit the growth of bladder tumors

Cancer Biol Ther. 2020 Dec 1;21(12):1171-1178. doi: 10.1080/15384047.2020.1844115. Epub 2020 Nov 20.

Abstract

Bladder cancer is a common and widespread cancer of the human urinary system, and its incidence is increasing. Gene therapy is a promising treatment of bladder cancer. In our study, a recombinant adeno-associated virus (rAAV9-UPII-TK-EGFP) driven by a UPII promoter was constructed. The efficacy and safety of infection of bladder cells was tested in vivo and in vitro. The ability of rAAV9-UPII-TK-EGFP to penetrate the glycosaminoglycan (GAG) layer on the surface of bladder cells and to transduce the bladder cells in vivo was very high. Additionally, we confirmed that the TK/GCV system has a powerful cytotoxic effect on bladder tumor cells in vitro and in vivo. Thus, our data indicate that rAAV9-UPII-TK-EGFP is a precise gene drug delivery system for the treatment of bladder cancer, and the TK/GCV therapeutic strategy has a powerful antitumor effect. These findings can be widely used in clinical and scientific studies.

Keywords: Bladder cancer; adeno associated virus; gene therapy; glycosaminoglycan layer; suicide gene.

MeSH terms

  • Animals
  • Female
  • Genes, Transgenic, Suicide / genetics*
  • Genetic Therapy / methods*
  • Green Fluorescent Proteins / metabolism*
  • Humans
  • Mice
  • Urinary Bladder Neoplasms / genetics*

Substances

  • enhanced green fluorescent protein
  • Green Fluorescent Proteins