TY - JOUR
T1 - Biphasic effects of zeranol on the growth of estrogen receptor-positive human breast carcinoma cells
AU - Yuri, Takashi
AU - Tsukamoto, Reiko
AU - Miki, Katsuaki
AU - Uehara, Norihisa
AU - Matsuoka, Yoichiro
AU - Tsubura, Airo
PY - 2006/12
Y1 - 2006/12
N2 - Zeranol (α-zearalanol) is a metabolite of the mycoestrogen zearalenone, and is used as a growth promoter of livestock due to its strong estrogenic activity. In the present study, we investigated the effects of zeranol on the growth of estrogen receptor (ER)-positive and -negative human breast carcinoma cells in vitro, and the molecules involved. At low concentrations, zeranol accelerated the growth of ER-positive MCF-7 and KPL-1 human breast carcinoma cells, but did not affect the growth of ER-negative MDA-MB-231 cells. At high concentrations, zeranol suppressed the growth of both ER-positive and -negative human breast carcinoma cells. The acceleration of ER-positive cell growth by low-dose zeranol involved the down-regulation of p21Cip1 (a cyclin-dependent kinase inhibitor), which resulted in cell cycle progression. High-dose zeranol induced the formation of a sub-G1 fraction and the up-regulation of the apoptosis stimulator p53, suggesting the induction of apoptosis. Thus, zeranol exerted dose-dependent biphasic effects on ER-positive human breast carcinoma cells, accelerating cell growth at low concentrations and inducing apoptosis at high concentrations.
AB - Zeranol (α-zearalanol) is a metabolite of the mycoestrogen zearalenone, and is used as a growth promoter of livestock due to its strong estrogenic activity. In the present study, we investigated the effects of zeranol on the growth of estrogen receptor (ER)-positive and -negative human breast carcinoma cells in vitro, and the molecules involved. At low concentrations, zeranol accelerated the growth of ER-positive MCF-7 and KPL-1 human breast carcinoma cells, but did not affect the growth of ER-negative MDA-MB-231 cells. At high concentrations, zeranol suppressed the growth of both ER-positive and -negative human breast carcinoma cells. The acceleration of ER-positive cell growth by low-dose zeranol involved the down-regulation of p21Cip1 (a cyclin-dependent kinase inhibitor), which resulted in cell cycle progression. High-dose zeranol induced the formation of a sub-G1 fraction and the up-regulation of the apoptosis stimulator p53, suggesting the induction of apoptosis. Thus, zeranol exerted dose-dependent biphasic effects on ER-positive human breast carcinoma cells, accelerating cell growth at low concentrations and inducing apoptosis at high concentrations.
UR - http://www.scopus.com/inward/record.url?scp=35648986968&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=35648986968&partnerID=8YFLogxK
U2 - 10.3892/or.16.6.1307
DO - 10.3892/or.16.6.1307
M3 - Article
C2 - 17089054
AN - SCOPUS:35648986968
SN - 1021-335X
VL - 16
SP - 1307
EP - 1312
JO - Oncology reports
JF - Oncology reports
IS - 6
ER -