A human adenoviral vector with a chimeric fiber from canine adenovirus type 1 results in novel expanded tropism for cancer gene therapy.

The development of novel therapeutic strategies is imperative for the treatment of advanced cancers like ovarian cancer and glioma, which are resistant to most traditional treatment modalities. In this regard, adenoviral (Ad) cancer gene therapy is a promising approach. However, the gene delivery efficiency of human serotype 5 recombinant adenoviruses (Ad5) in cancer gene therapy clinical trials to date has been limited, mainly due to the paucity of the primary Ad5 receptor, the coxsackie and adenovirus receptor (CAR), on human cancer cells. To circumvent CAR deficiency, Ad5 vectors have been retargeted by creating chimeric fibers possessing the knob domains of alternate human Ad serotypes. Recently, more radical modifications based on 'xenotype' knob switching with non-human adenovirus have been exploited. Herein, we present the characterization of a novel vector derived from a recombinant Ad5 vector containing the canine adenovirus serotype 1 (CAV-1) knob (Ad5Luc1-CK1), the tropism of which has not been previously described. We compared the function of this vector with our other chimeric viruses displaying the CAV-2 knob (Ad5Luc1-CK2) and Ad3 knob (Ad5/3Luc1). Our data demonstrate that the CAV-1 knob can alter Ad5 tropism through the use of a CAR-independent entry pathway distinct from that of both Ad5Luc1-CK2 and Ad5/3-Luc1. In fact, the gene transfer efficiency of this novel vector in ovarian cancer cell lines, and more importantly in patient ovarian cancer primary tissue slice samples, was superior relative to all other vectors applied in this study. Thus, CAV-1 knob xenotype gene transfer represents a viable means to achieve enhanced transduction of low-CAR tumors.
AuthorsM A Stoff-Khalili, A A Rivera, J N Glasgow, L P Le, A Stoff, M Everts, Y Tsuruta, Y Kawakami, G J Bauerschmitz, J M Mathis, L Pereboeva, G P Seigal, P Dall, D T Curiel
JournalGene therapy (Gene Ther) Vol. 12 Issue 23 Pg. 1696-706 (Dec 2005) ISSN: 0969-7128 [Print] England
PMID16034451 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S.)
Chemical References
  • Capsid Proteins
  • DNA, Viral
  • hexon capsid protein, Adenovirus
  • Adenoviruses, Canine (genetics)
  • Binding, Competitive
  • Capsid Proteins (genetics)
  • Cell Line, Tumor
  • DNA, Viral
  • Female
  • Gene Expression
  • Genetic Engineering
  • Genetic Therapy (methods)
  • Genetic Vectors (administration & dosage, genetics)
  • Humans
  • Liver (metabolism, virology)
  • Neoplasms (therapy)
  • Ovarian Neoplasms (therapy)
  • Transduction, Genetic (methods)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research network!

Choose Username:
Verify Password: