Caspase-8 gene transduction augments radiation-induced apoptosis in DLD-1 cells

被引:16
作者
Uchida, H
Shinoura, N
Kitayama, J
Watanabe, T
Nagawa, H
Hamada, H
机构
[1] Sapporo Med Univ, Dept Mol Med, Chuo Ku, Sapporo, Hokkaido 0608556, Japan
[2] Univ Tokyo, Dept Surg, Div Surg Oncol, Bunkyo Ku, Tokyo 1138655, Japan
[3] Tokyo Metropolitan Komagome Hosp, Dept Neurosurg, Bunkyo Ku, Tokyo 1130021, Japan
关键词
apoptosis; caspase-8; radiation; gene therapy; colorectal cancer;
D O I
10.1006/bbrc.2002.6643
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Caspase-8 is a member of the cysteine protease family that plays a critical role in death receptor-mediated apoptosis. We previously demonstrated that adenovirally transduced caspase-8 efficiently induced apoptosis in tumor cells (Shinoura et al. (2000) Hun. Gene Ther. 11, 1123-1137). However, to ensure safety in clinical applications some devise for minimization of the dose of adenoviral vector required for sufficient antitumor effect is needed. In this study, we evaluated the proapoptotic effect in DLD-1 colon cancer cells of a combination of low-dose infection with an adenoviral vector expressing caspase-8 and X-ray irradiation. Under these conditions, X-ray irradiation strongly induced apoptosis whereas irradiation without transduction only had a trace proapoptotic effect. Overexpression of bcl-xL strongly blocked the activation of caspase-8 and induction of apoptosis, suggesting that adenovirally transduced caspase-8 was activated at a point downstream of mitochondria. This combination strategy may be a useful modality for gene therapy of colorectal cancer. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:347 / 354
页数:8
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