| Literature DB >> 10637446 |
K Yamabe1, S Shimizu, T Ito, Y Yoshioka, M Nomura, M Narita, I Saito, Y Kanegae, H Matsuda.
Abstract
Caspase-3 is a member of the cysteine protease family, which plays a crucial role in apoptosis. We applied the human caspase-3 gene as a novel form of anticancer gene therapy. Overexpression of human caspase-3 alone could not induce apoptosis of tumor cell lines, but apoptosis was markedly enhanced by the addition of etoposide. In an AH130 liver tumor model, transduction of human caspase- 3, but not the empty vector, induced extensive apoptosis and reduced tumor volume when combined with etoposide administration. However, this effect was not observed with a Bcl-2 overexpressing tumor. In conclusion, caspase-3 gene transduction accompanied by an additional death stimulus may be a useful method of anticancer gene therapy, except for Bcl-2 overexpressing tumors.Entities:
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Year: 1999 PMID: 10637446 DOI: 10.1038/sj.gt.3301041
Source DB: PubMed Journal: Gene Ther ISSN: 0969-7128 Impact factor: 5.250