Suppression of pulmonary metastasis using adenovirally motility related protein-1 (MRP-1/CD9) gene delivery

被引:45
作者
Miyake, M
Inufusa, H
Adachi, M
Ishida, H
Hashida, H
Tokuhara, T
Kakehi, Y
机构
[1] Kitano Hosp, Tazuke Kofukai Med Res Inst, Dept Thorac Surg, Kita Ku, Osaka 5308480, Japan
[2] Kitano Hosp, Tazuke Kofukai Med Res Inst, Dept Oncol 5, Kita Ku, Osaka 5308480, Japan
[3] Kinki Univ, Sch Med, Dept Surg 1, Osaka 5898511, Japan
[4] Kyoto Univ, Dept Urol & Pathol, Kyoto 6068501, Japan
关键词
MRP-1/CD9; adenovirus; gene therapy; metastasis;
D O I
10.1038/sj.onc.1203919
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
Previously we showed that MRP-1/CD9 might prevent tumor metastasis by suppression of cell motility and invasion of tissue barriers. The present study explored the possibility of preventing metastasis of mouse melanoma BL6 by expression of MRP-1/CD9 through gene transfer. A replication-deficient adenovirus vector was used for the in vivo transfer of MRP-1/CD9 cDNA, Intratumor injection of an adenovirus vector (rAd-MRP-1/CD9) expressing MRP-1/CD9 resulted in a 73.7% reduction in the number of pulmonary metastases of mice and the median survival time of mice treated with rAd-MRP-1/CD9 was significantly longer than those treated with the rAd-beta -gal vector (103.2+/-8.5 days vs 71.2+/-5.2 days, P<0.001 respectively). These results support the expression of MRP-1/CD9 through gene transfer as a therapeutic strategy for preventing metastases and prolonging survival, and support the feasibility of gene transfer in a clinically relevant setting.
引用
收藏
页码:5221 / 5226
页数:6
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