Estrogen receptor-α regulates SOCS-3 expression in human breast cancer cells

被引:33
作者
Matthews, J [1 ]
Almlöf, T
Kietz, S
Leers, J
Gustafsson, JÅ
机构
[1] Novum, Karolinska Inst, Dept Biosci, S-14157 Huddinge, Sweden
[2] Novum, Karolinska Inst, Dept Med Nutr, S-14186 Huddinge, Sweden
关键词
estrogen receptor; SOCS-3; cytokine; STAT; chromatin immunoprecipitation; nuclear receptor; promoter cloning;
D O I
10.1016/j.bbrc.2005.07.057
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The suppressor of cytokine signalling (SOCS) protein family negatively regulates cytokine action. In this study, we investigated the effects of estrogen (E2) on SOCS-3 expression in T47D and MCF-7 human breast cancer cells. Real-time PCR analysis of E2-treated T47D cells revealed a ligand and time-dependent increase in of SOCS-3 mRNA levels. Cloning of a 1.7 kb fragment of the human SOCS-3 5' flanking sequence, and subsequent analysis of potential transcription factor-binding sites identified an incomplete ERE motif located - 1493 to - 1489 upstream of the start site. Transient transfection of the cloned fragment in MCF-7 cells showed that both E2 and genistein treatment caused an increase in reporter gene activity, which was inhibited by co-treatment with ICI 182,780. Chromatin immunoprecipitation analysis revealed an E2 and time-dependent recruitment of ER alpha to the E2 responsive region of the human SOCS-3 promoter. In summary, this study shows that ER alpha directly regulates human SOCS-3 promoter activity in human breast cancer cells, thus modulating cytokine activity. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:168 / 174
页数:7
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