The p53 tumor suppressor gene functions through the p53-mediated transcript
ional activation and regulation of critical downstream target genes, The me
chanism behind such regulation, however, remains unclear. In this study, we
compared the expression of 30 genes that are involved in cell cycle checkp
oint control and/or apoptosis in a human lung cancer cell line, which conta
ins endogenous wild-type p53, in response to ectopic p53 expression. Of the
30 genes studied, 22 genes have shown an increase in expression. The incre
ase in gene expression of 2 genes-Gadd45 and PIG2-was more than 10-fold. Th
ese results suggest that the genes with the highest expression level in a p
53-dependent pathway may play a dominant role in determining the pathway th
at the cell follows: cell cycle arrest or apoptosis, Our screen illustrates
the development of a simple and inexpensive p53-specific cDNA array to beg
in to analyze downstream events in the p53 pathway under physiological, pat
hological, and stress-induced states. (C) 1999 Academic Press.