Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/19864
Title: Activation of insulin-like growth factor I receptor-mediated pathway by ginsenoside Rg1
Authors: Chen, WF
Lau, WS
Cheung, PY
Guo, DA
Wong, MS 
Keywords: Estrogen
Ginsenoside Rg1
Human breast cancer
Insulin-like growth factor I receptor
Phytoestrogen
Issue Date: 2006
Publisher: Wiley-Blackwell
Source: British journal of pharmacology, 2006, v. 147, no. 5, p. 542-551 How to cite?
Journal: British journal of pharmacology 
Abstract: Ginsenoside Rg1, an active ingredient in ginseng, was previously shown to be a novel class of potent phytoestrogen. The present study aims at investigating the molecular mechanisms involved in mediating its actions in human breast cancer (MCF-7) cells. Rg1 (1 pM) stimulates cell proliferation (P<0.01) and estrogen-responsive pS2 mRNA expression (P<0.05) without alteration of estrogen receptor alpha (ERα) protein or mRNA expression in MCF-7 cells. In addition, 10 -14-10 -4 M of Rg1 does not demonstrate specific binding to ERα. We hypothesize that Rg1 may exert its actions in MCF-7 cell via the activation of crosstalk between ER- and insulin growth factor I receptor (IGF-IR)-dependent pathways. The results indicate that Rg1 significantly increases IGF-IR expression and IGF-IR promoter activity in MCF-7 cells (P<0.05). Cotreatment of MCF-7 cells with 1 μM of estrogen antagonist ICI 182,780 completely abolishes the effects of Rg1 on IGF-IR expression. Furthermore, Rg1 enhances tyrosine phosphorylation of IRS-1 in MCF-7 cells upon IGF-I stimulation and the activation of IRS-1 phosphorylation is also ER-dependent. Taken together, our results suggest that Rg1 not only increases IGF-IR expression but also enhances IGF-IR-mediated signaling pathways in MCF-7 cells. The stimulation of IGF-IR expression by Rg1 in MCF-7 cells appears to require ER, and its actions might involve ligand-independent activation of ER.
URI: http://hdl.handle.net/10397/19864
ISSN: 0007-1188
EISSN: 1476-5381
DOI: 10.1038/sj.bjp.0706640
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