Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10768351 | Biochemical and Biophysical Research Communications | 2005 | 7 Pages |
Abstract
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 5â² flanking sequence, and subsequent analysis of potential transcription factor-binding sites identified an incomplete ERE motif located â1493 to â1489 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 ERα to the E2 responsive region of the human SOCS-3 promoter. In summary, this study shows that ERα directly regulates human SOCS-3 promoter activity in human breast cancer cells, thus modulating cytokine activity.
Related Topics
Life Sciences
Biochemistry, Genetics and Molecular Biology
Biochemistry
Authors
Jason Matthews, Tova Almlöf, Silke Kietz, Jörg Leers, Jan-Ã
ke Gustafsson,