STIMULATION OF C-MYC ONCOGENE EXPRESSION ASSOCIATED WITH ESTROGEN-INDUCED PROLIFERATION OF HUMAN-BREAST CANCER-CELLS

  • 15 December 1987
    • journal article
    • research article
    • Vol. 47  (24) , 6517-6521
Abstract
Regulation of c-myc expression is known to be sensitive to a variety of mitogenic stimuli in various cell types. Since estrogen is a well documented mitogen of estrogen-responsive human breast cancer (HBC) cells, we studied the influence of estradiol and its antagonist tamoxifen on the expresion of c-myc in HBC cell lines. Using Northern hybridization analysis, we monitored the accumulation of c-myc mRNA in a number of HBC cell lines. The cell lines studied included the estrogen-responsive, estrogen receptor positive (ER+) MCF-7, T-47D, the nonresponsive, estrogen receptor negative (ER-) MDA-MB-231, BT-20, and a nontumorous breast cell line, HBL-100. The effects of endogenous estrogen were minimized by culturing the cells in medium containing 10% (v/v) charcoal-treated fetal bovine serum and tamoxifen (10-6 M)for 48 h prior to estradiol (10-7 M) treatment. In the ER+ cell lines the addition of estradiol resulted in a noticeable increase in c-myc expression after 15 min with a maximal (> 10-fold) induction in 1-2 h. In the ER- cell lines the level of c-myc mRNA was high and was unaffected by estrogen tamoxifen; in the ER- cancer cell lines, neither amplification nor rearragement of the c-myc gene was observed. In contrast, the expression of another oncogene, c-H-ras, remained constant in both ER+ and ER- cell lines and was insensitive to estrogen and antiestrogen. These results suggest that the regulation of c-myc expression may be an important step in estrogen-induced proliferation ofHBC cells.