Adenovirus-mediated REIC/Dkk-3 gene transfer inhibits tumor growth and metastasis in an orthotopic prostate cancer model

被引:61
作者
Edamura, K.
Nasu, Y.
Takaishi, M.
Kobayashi, T.
Abarzua, F.
Sakaguchi, M.
Kashiwakura, Y.
Ebara, S.
Saika, T.
Watanabe, M.
Huh, N-H
Kumon, H.
机构
[1] Okayama Univ, Grad Sch Med Dent Pharmaceut Sci, Dept Urol, Okayama 7008558, Japan
[2] Okayama Univ, Grad Sch Med Dent Pharmaceut Sci, Dept Cell Biol, Okayama 7008558, Japan
[3] Okayama Univ Hosp, Ctr Gene & Cell Therapy, Okayama, Japan
基金
日本学术振兴会;
关键词
Dkk-3; REIC; prostate cancer; apoptosis; metastasis; invasion;
D O I
10.1038/sj.cgt.7701071
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 0836 [生物工程]; 090102 [作物遗传育种]; 100705 [微生物与生化药学];
摘要
We had previously reported that REIC/Dkk-3, a member of the Dickkopf ( Dkk) gene family, works as a tumor suppressor. In this study, we evaluated the therapeutic effects of an intratumoral injection with adenoviral vector encoding REIC/Dkk-3 gene ( Ad-REIC) using an orthotopic mouse prostate cancer model of RM-9 cells. We also investigated the in vivo anti-metastatic effect and in vitro anti-invasion effect of Ad-REIC gene delivery. We demonstrated that the Ad-REIC treatment inhibited prostate cancer growth and lymph node metastasis, and prolonged mice survival in the model. These therapeutic responses were consistent with the intratumoral apoptosis induction and in vitro suppression of cell invasion/migration with reduced matrix metalloprotease-2 activity. We thus concluded that in situ Ad-REIC/Dkk-3 gene transfer may be a promising therapeutic intervention modality for the treatment of prostate cancer.
引用
收藏
页码:765 / 772
页数:8
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