| Literature DB >> 16456550 |
R M Tjin Tham Sjin1, J Naspinski, A E Birsner, C Li, R Chan, K-M Lo, S Gillies, D Zurakowski, J Folkman, J Samulski, K Javaherian.
Abstract
Developing continuous systemic delivery of endostatin has been a goal of many laboratories. We have employed a method of gene therapy utilizing different viral constructs. Here, we report that a new serotype of adeno-associated viruses, which incorporates canine endostatin, provides dose-dependent transgene expression in the circulation after intramuscular injection in mice. Elevated levels of endostatin remained stable in the circulation for at least 4 months. In vitro assays determined that the protein expressed was biologically active. Antitumor activities of the above construct demonstrated a U-shape curve, where the maximum activity was observed within a certain critical concentration range. These data suggest that an optimum dose range may be required to achieve therapeutic efficacy in large animal models.Entities:
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Year: 2006 PMID: 16456550 DOI: 10.1038/sj.cgt.7700938
Source DB: PubMed Journal: Cancer Gene Ther ISSN: 0929-1903 Impact factor: 5.987