Pn. Huynh et al., 17 Alpha androstenediol inhibition of breast tumor cell proliferation in estrogen receptor-positive and -negative cell lines, CANCER DET, 24(5), 2000, pp. 435-444
Androstene-3 beta, 17 alpha -diol (17 alpha -AED) inhibits DNA synthesis an
d induces apoptosis in several myeloid cancer cell lines. The purpose of th
is study was to determine if 17 alpha -AED inhibition of human breast carci
noma cell proliferation is dependent on the estrogen or androgen receptor.
At concentrations of 12.5 to 50 x 10(-9) M 17 alpha -AED inhibited the prol
iferation of ZR75-1, estrogen receptor-positive (ER+) cells, by 54% to 68%.
Further, 17 alpha -AED inhibited MDA-MB231, estrogen receptor-negative (ER
-) cells, by 33.6% to 56.0%. The inhibitory effect was dose dependent with
a minimal effective inhibitory dose at 12.5 x 10-9 M for both cell Lines. B
oth 17 beta -AED and estradiol potentiate the inhibitory effect of 17 alpha
-AED on ER+ cells at lower doses (3.13 to 6.25 x 10(-9) M) where 17 alpha
-AED alone was not inhibitory. The inhibitory action of 17 alpha -AED on hu
man mammary carcinomas appears to be independent of either the alpha estrog
en or the androgen receptors.