Resveratrol acts as an estrogen receptor (ER) agonist in breast cancer cells stably transfected with ERα

被引:83
作者
Levenson, AS
Gehm, BD
Pearce, ST
Horiguchi, J
Simons, LA
Ward, JE
Jameson, JL
Jordan, VC
机构
[1] Northwestern Univ, Feinberg Sch Med, Robert H Lurie Comprehens Canc Ctr, Chicago, IL 60611 USA
[2] Northwestern Univ, Feinberg Sch Med, Div Endocrinol Metab & Mol Med, Chicago, IL 60611 USA
[3] Northwestern Univ, Feinberg Sch Med, Robert H Lurie Comprehens Canc Ctr, Chicago, IL 60611 USA
关键词
resveratrol; ER alpha; agonistic activity; gene arrays; p21(CIP1/WAF1); breast cancer cells;
D O I
10.1002/ijc.10992
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Resveratrol (Res) is a phytoestrogen found in grapes and present in red wine. Res has been shown to function as an estrogen receptor (ER) agonist, but it remains unclear whether it may also exert antagonist activity. Our aim was to study the effects of Res at both the molecular (TGFalpha gene activation) and the cellular (cell growth) levels in breast cancer cells stably transfected with wild-type (wt) ER(D35 1) and mutant (mut) ER (D35 I Y). TGFalpha mRNA induction was used as a specific marker of estradiol (E-2) responsiveness. Res caused a concentration-dependent ( 10(-8)-10(-4) M) stimulation of TGFalpha mRNA, indicating that it acts as an estrogen agonist in these cell lines. The pure antiestrogen ICI 182,780 (ICI) blocked Res-induced activation of TGFalpha, consistent with action through an ER-mediated pathway. Further studies that combined treatments with E-2 and Res showed that Res does not act as an antagonist in the presence of various (10(-11)-10(-8) M) concentrations of E-2. To determine whether Res can be classified as a type I or type 11 estrogen (Jordan et al., Cancer Res 200 1;61:6619-23,), we examined Res with the D35 I G ER in the TGFalpha assay and found that Res belongs to the type I estrogens. Both Res and E, had concentration-dependent growth inhibitory effects in cells expressing wtER and D35 I Y ER. Although the pure antiestrogen ICI blocked the growth inhibitory effects of E-2, it did not block the inhibitory effects of Res, suggesting that the antiproliferative effects of Res also involve. ER-independent pathways. Interestingly, Res differentially affected the levels of ER protein in these 2 cell lines: Res down-regulated wtER levels while significantly up-regulating the amount of mutD351Y ER. Co-treatment with ICI resulted in strongly reduced ER levels in both cell lines. Gene array studies revealed Res-induced upregulation of more than 80 genes, among them a profound activation of p21(CIP1)/WAF1, a gene associated with growth arrest. The p21(CIP1)/WAF1 protein levels measured by Western blotting confirmed Res-induced significant up-regulation of this protein in both cell lines. In summary, Res acts as an ER agonist at low doses but also activates ER-independent pathways, some of which inhibit cell growth. 0 2003 Wiley-Liss, Inc.
引用
收藏
页码:587 / 596
页数:10
相关论文
共 71 条
[1]   DIETARY PHYTOESTROGENS AND CANCER - INVITRO AND INVIVO STUDIES [J].
ADLERCREUTZ, H ;
MOUSAVI, Y ;
CLARK, J ;
HOCKERSTEDT, K ;
HAMALAINEN, E ;
WAHALA, K ;
MAKELA, T ;
HASE, T .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1992, 41 (3-8) :331-337
[2]  
Ahmad N, 2001, CLIN CANCER RES, V7, P1466
[3]   Proteasome-mediated proteolysis of estrogen receptor: A novel component in autologous down-regulation [J].
Alarid, ET ;
Bakopoulos, N ;
Solodin, N .
MOLECULAR ENDOCRINOLOGY, 1999, 13 (09) :1522-1534
[4]   Estrogen receptor β-selective transcriptional activity and recruitment of coregulators by phytoestrogens [J].
An, JP ;
Tzagarakis-Foster, C ;
Scharschmidt, TC ;
Lomri, N ;
Leitman, DC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (21) :17808-17814
[5]  
Ashby J, 1999, J APPL TOXICOL, V19, P39, DOI 10.1002/(SICI)1099-1263(199901/02)19:1&lt
[6]  
39::AID-JAT534&gt
[7]  
3.0.CO
[8]  
2-M
[9]  
Banerjee S, 2002, CANCER RES, V62, P4945
[10]   Estrogenic/antiestrogenic and scavenging properties of (E)- and (Z)-resveratrol [J].
Basly, JP ;
Marre-Fournier, F ;
Le Bail, JC ;
Habrioux, G ;
Chulia, AJ .
LIFE SCIENCES, 2000, 66 (09) :769-777