Retinoic acid (RA). modulation of c-myc and max gene expression was in
vestigated in human breast carcinoma (HBC) cell lines. Our results dem
onstrate that c-myc and max genes are differentially expressed in HBC
cells which was accompanied by increases in [H-3]-thymidine incorporat
ion and percent of cells in the S phase of cell cycle. RA-mediated inc
rease in c-myc mRNA levels were noticed as early as 30 min. and maximu
m levels were attained by 1 h. RA effect on max mRNA levels was slow a
nd gradual with the maximum effect noticed by 48 h. Nuclear run-on ass
ays demonstrated that RA mediated its effect by increasing the rate of
transcription of both of these genes. We thus report for the first ti
me that RA, during its growth inhibitory effects on MCF-7 HBC cells, p
ositively regulates the gene expression of c-myc and max.