Adenovirus-mediated p16INK4 gene transfer significantly suppresses human breast cancer growth

被引:20
|
作者
Campbell, I
Magliocco, A
Moyana, T
Zheng, CY
Xiang, J [1 ]
机构
[1] Univ Saskatchewan, Saskatoon Canc Ctr, Dept Microbiol, Saskatoon, SK S7N 4H4, Canada
[2] Univ Saskatchewan, Saskatoon Canc Ctr, Dept Pathol, Saskatoon, SK S7N 4H4, Canada
[3] Univ Calgary, Dept Pathol, Calgary, AB, Canada
[4] NIDR, Gene Therapy Branch, NIH, Bethesda, MD 20892 USA
基金
英国医学研究理事会;
关键词
p16; adenovirus; apoptosis; breast cancer;
D O I
10.1038/sj.cgt.7700226
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 ; 0836 ; 090102 ; 100705 ;
摘要
The p16(INK4) tumor suppressor gene encodes a protein that inhibits cyclin-dependent kinase 4, and its homologous deletion is common in human breast cancer. p16(INK4) gene transfer has been reported to be efficacious in inducing growth inhibition of various human tumors such as brain, lung, prostate, and esophageal cancers. However, the efficiency of the p16(INK4) gene with regard to growth inhibition of human breast cancer has not been studied extensively. To examine its tumor-suppressive function and its potential in breast cancer gene therapy, the wild-type p16(INK4) gene was expressed in an adenovirus-mediated gene delivery system and introduced into breast cancer cell lines that do not express p16(INK4) protein. Expression of the introduced p16(INK4) blocked tumor cell entry into the S phase of the cell cycle, induced tumor cell apoptosis, and inhibited tumor cell proliferation both in vitro and in vivo. These results strongly suggest that p1(INK4) is a tumor suppressor gene and suggest that ii has potential utility in breast cancer gene therapy.
引用
收藏
页码:1270 / 1278
页数:9
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