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Oncogene ; 31(49): 5073-80, 2012 Dec 06.
Article in English | MEDLINE | ID: mdl-22286763

ABSTRACT

The 40S ribosomal S6 kinase 1 (S6K1) is an important regulator of cell growth. Expression of S6K1 is often elevated in breast cancer cells. However, the transcriptional mechanism of S6K1 overexpression is not understood. In this report, we demonstrate that estrogen activates expression of S6K1 via estrogen receptor (ER)α in ER-positive breast cancer cells. We also show that estrogen acts on the proximal promoter of the S6K1 gene in a mechanism involving the transcriptional factor GATA-3. Finally, we provide data that support the importance of estrogenic regulation of S6K1 expression in breast cancer cell proliferation. S6K1 directly phosphorylates and regulates ligand-independent activity of ERα, while ERα upregulates S6K1 expression. This S6K1-ERα relationship creates a positive feed-forward loop in control of breast cancer cell proliferation. Furthermore, the co-dependent association between S6K1 and ERα may be exploited in the development of targeted breast cancer therapies.


Subject(s)
Breast Neoplasms/pathology , Estrogen Receptor alpha/metabolism , Gene Expression Regulation, Neoplastic , Ribosomal Protein S6 Kinases, 70-kDa/genetics , Animals , Breast Neoplasms/genetics , Breast Neoplasms/metabolism , Cell Proliferation , Estradiol/pharmacology , Estrogen Receptor alpha/genetics , Feedback, Physiological , Female , GATA3 Transcription Factor/genetics , GATA3 Transcription Factor/metabolism , Humans , MCF-7 Cells , Mammary Glands, Animal/drug effects , Mammary Glands, Animal/metabolism , Mice , Mice, Inbred Strains , Phosphorylation , Promoter Regions, Genetic , Ribosomal Protein S6 Kinases, 70-kDa/metabolism , Tamoxifen/analogs & derivatives , Tamoxifen/pharmacology
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