Estrogen receptor β inhibits 17β-estradiol-stimulated proliferation of the breast cancer cell line T47D

被引:466
作者
Ström, A
Hartman, J
Foster, JS
Kietz, S
Wimalasena, J
Gustafsson, JA [1 ]
机构
[1] Karolinska Inst, Novum, Dept Med Nutr & Biosci, S-14186 Huddinge, Sweden
[2] Karolinska Inst, Novum, Dept Biosci, S-14157 Huddinge, Sweden
[3] Univ Tennessee, Med Ctr, Grad Sch Med, Dept Obstet & Gynecol, Knoxville, TN 37920 USA
关键词
cell cycle; p27; cyclin E; Cdc25A; Cdk2;
D O I
10.1073/pnas.0308319100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Estrogen receptor (ER) 13 counteracts the activity of ERalpha in many systems. In agreement with this, we show in this study that induced expression of ERbeta in the breast cancer cell line T47D reduces 17beta-estradiol-stimulated proliferation when expression of ERbeta mRNA equals that of ERalpha. Induction of ERbeta reduces growth of exponentially proliferating cells with a concomitant decrease in components of the cell cycle associated with proliferation, namely cyclin E, Cdc25A (a key regulator of Cdk2), p45(Skp2) (a key regulator of p27(Kip1) proteolysis), and an increase in the Cdk inhibitor p27(Kip1). We also observed a reduced Cdk2 activity. These findings suggest a possible role for ERbeta in breast cancer and imply that ERbeta-specific ligands may reduce proliferation of ER-positive breast cancer cells through actions on the G(1) phase cell-cycle machinery.
引用
收藏
页码:1566 / 1571
页数:6
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