Lap. Hoogenboon et al., Estrogenic activity of estradiol and its metabolites in the ER-CALUX assaywith human T47D breast cells, APMIS, 109, 2001, pp. S480-S486
A number of metabolites of 17 beta -estradiol were tested for their estroge
nic activity using the ER-CA-LUX assay based on the increased expression of
luciferase in exposed T47D breast cancer cells. E(2)beta and estrone showe
d similar potencies in the test, whereas E(2)alpha was 100 times less activ
e. Incubation of cells with estrone (0.35 muM) resulted in the formation of
E(2)beta, whereas the reverse reaction was observed for E(2)beta. The resu
lting equilibrium may explain the similar estrogenic potency of estrone in
the test. The synthetic 17-hydroxy benzoate ester of E(2)beta was 3 times l
ess active than the parent compound. The 17-hydroxy palmitate and oleate es
ters of E(2)beta, were respectively 25 and 200 times less active than the p
arent compound. The 2-hydroxy metabolites of E(2)beta and estrone showed a
5,000 to 10,000 fold lower activity The 4-hydroxy metabolites were more pot
ent than the 2-hydroxy metabolites, showing only a 20-200 times lower activ
ity. The 2- and 4-methoxyesters of estrone were 700 times less active. It i
s concluded that the estrogenic potency of metabolites formed in cattle aft
er treatment with E(2)beta, like estrone, E(2)alpha and especially the este
rs of E(2)beta may be significant with respect to the potential risk of the
use of estradiol for growth promotion in domestic animals in certain count
ries.