DOWN-REGULATION OF BCL-2 BY P53 IN BREAST-CANCER CELLS

bcl-2 and p53 gene products have been both linked to programmed cell d eath pathways. We have analyzed several human breast cancer cell lines for the expression of bcl-2 and p53. We found an inverse correlation between the expression of the two proteins. The result suggested that mutant p53 could substitute for bcl-2 function in breast cancer cells and that could also down-regulate bcl-2 expression. We found, indeed, that overexpression of a mutant p53 (mut 175) in MCF-7 cells could ind uce down-regulation of bcl-2 both at protein and mRNA level. However, the promoter region of the human bcl-2 gene does not contain the negat ive regulatory element responsible for the down-regulation. If this me chanism will be proved also for the wild-type p53 allele, it may discl ose a possible mechanism for p53-induced apoptosis: down-regulation of bcl-2.