Gene expression profiling of p53-sensitive and -resistant tumor cells using DNA microarray

被引:7
作者
Maxwell, SA [1 ]
Davis, GE [1 ]
机构
[1] Texas A&M Univ Syst, Hlth Sci Ctr, Coll Med, Dept Pathol & Lab Med, College Stn, TX 77843 USA
关键词
cDNA microarray; ECV-304; gene expression; p53; p53-resistant;
D O I
10.1023/B:APPT.0000018799.20120.38
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
Overexpression of wild-type p53 in ECV-304 tumor cells induced extensive apoptosis and the eventual death of nearly all of the cells. We generated ECV-304 cells resistant to p53-induced apoptosis as a strategy to identify novel genes that might be relevant to p53-mediated apoptosis. ECV-304 cells resistant to p53 were isolated by repeated infections with a recombinant p53 adenovirus and were designated as DECV. The expression of 5,730 genes in p53-resistant (DECV) and p53-sensitive ECV-304 cells were profiled by DNA microarray analysis. We report here the expression of 80 genes that differed by 2-fold or more between sensitive and resistant cells upregulated for p53. Many of these differentially expressed genes are regulated by p53 in ECV-304 and H1299 p53-null cells. Our analysis identifies many new potential targets for p53 that play roles in cell cycle regulation, DNA repair, redox control, cell adhesion, apoptosis, and differentiation.
引用
收藏
页码:171 / 179
页数:9
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