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Hennessy, BA, Harvey, BJ, Healy, V;
2005
January
Molecular and Cellular Endocrinology
17 beta-estradiol rapidly stimulates c-fos expression via the MAPK pathway in T84 cells
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17 beta-estradiol estrogen receptor MAPK pathway c-fos western blotting BREAST-CANCER CELLS ESTROGEN RESPONSE ELEMENT TRANSCRIPTION FACTORS HUMAN COLON EPITHELIAL-CELLS GENE-EXPRESSION ER-ALPHA RECEPTOR ACTIVATION ESTRADIOL
229
39
47

In this study, we show that 17beta-Estradiol (E2) induced the proliferation of T84 colonic carcinoma cells. We further, investigated the mechanisms underlying this proliferation and show that E2 induced c-fos protooncogene expression in T84 cells in a timescale consistent with a rapid non-genomic action of the hormone. Furthermore, E2 rapidly phosphorylated both CREB and ELK1, transcription factors that bind to the c-fos promoter and stimulate transcription. Pretreatment with PD98059 and H89. mitogen-activated protein kinase (MAPK) pathway and protein kinase A (PKA) inhibitors. respectively showed that phosphorylation of CREB and ELK1 and subsequent c-fos induction was mediated by the MAPK pathway only. Finally, the estrogen receptor (ER) antagonist, ICI 182.780, blocked the activation of MAPK pathway. subsequent CREB and ELK1 phosphorylation and c-fos induction in T84 cells suggesting an ER dependent mechanism. Consistent with ibis finding, ICI 182,780 caused a substantial reduction in the proliferative effects of E2 on T84 cells. (C) 2004 Elsevier Ireland Ltd. All rights reserved.

DOI 10.1016/j.mce.2004.10.001
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