A novel adenoviral vector expressing human Fas/CD95/APO-1 enhances p53-mediated apoptosis

被引:21
作者
Rakkar, ANS [1 ]
Katayose, Y [1 ]
Kim, M [1 ]
Craig, C [1 ]
Ohri, E [1 ]
Li, ZQ [1 ]
Cowan, KH [1 ]
Seth, P [1 ]
机构
[1] NCI, Med Breast Canc Sect, Med Branch, Div Clin Sci,NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
adenovirus; Fas/CD95/APO-1; p53; apoptosis; gene therapy;
D O I
10.1038/sj.cdd.4400498
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
Recent evidence suggests an intriguing link between p53 and the Fas pathway. To evaluate this association further, we utilized a recombinant adenoviral vector (AdWTp53) to overexpress wild-type p53 in lung cancer (A549, H23, EKVX and HOP92) and breast cancer(MDA-MB-231 and MCF-7) cell lines and observed an increase in the Fas/CD95/APO-1 protein levels. Furthermore, this increase correlated with the sensitivity of the cell lines to p53-mediated cytotoxicity, To examine the effects of Fas over-expression in cells resistant to p53 over-expression, we constructed AdFas, an adenoviral vector capable of transferring functional human Fas to cancer cells. Interestingly, infection of p53 resistant MCF-7 cells with AdFas sensitized them to p53-mediated apoptosis, These studies indicate that combined over-expression of Fas and wild-type p53 may be an effective cancer gene therapy approach, especially in cells relatively resistant to p53 overexpression.
引用
收藏
页码:326 / 333
页数:8
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