ginsenoside-rh1 and Breast-Neoplasms

ginsenoside-rh1 has been researched along with Breast-Neoplasms* in 1 studies

Other Studies

1 other study(ies) available for ginsenoside-rh1 and Breast-Neoplasms

ArticleYear
A ginsenoside-Rh1, a component of ginseng saponin, activates estrogen receptor in human breast carcinoma MCF-7 cells.
    The Journal of steroid biochemistry and molecular biology, 2003, Volume: 84, Issue:4

    We have examined the possibility that a component of Panax ginseng, ginsenoside-Rh1, acts by binding to steroid hormone receptors such as receptors for estrogen, glucocorticoid, androgen, and retinoic acid. Ginsenoside-Rh1 activated the transcription of the estrogen-responsive luciferase reporter gene in MCF-7 breast cancer cells at a concentration of 50 microM. Activation was inhibited by the specific estrogen receptor antagonist ICI 182,780, indicating that the estrogenic effect of ginsenoside-Rh1 is estrogen receptor dependent. Ginsenoside-Rh1 induction of luciferase activity was dose-dependent in CV-1 cells transiently transfected with estrogen receptor and reporter plasmids. Next, we evaluated the ability of ginsenoside-Rh1 to induce the estrogen-responsive genes in MCF-7 cells. Ginsenoside-Rh1 increased c-fos and pS2 at the mRNA levels at 24h after treatment, although the effects were not as prominent as 17beta-estradiol. Western blot analysis showed that progesterone receptor protein was induced at 24h of treatment of ginsenoside-Rh1. However, ginsenoside-Rh1 failed to activate the glucocorticoid receptor, the androgen receptor, or the retinoic acid receptor in CV-1 cells transiently transfected with the corresponding steroid hormone receptors and hormone responsive reporter plasmids. These data support our hypothesis that ginsenoside-Rh1 acts as a weak phytoestrogen, presumably by binding and activating the estrogen receptor.

    Topics: Blotting, Western; Breast Neoplasms; Dose-Response Relationship, Drug; Estradiol; Genes, Reporter; Ginsenosides; Humans; Luciferases; Membrane Proteins; Models, Chemical; Plasmids; Presenilin-2; Proto-Oncogene Proteins c-fos; Receptors, Androgen; Receptors, Estrogen; Receptors, Retinoic Acid; Reverse Transcriptase Polymerase Chain Reaction; Signal Transduction; Time Factors; Transfection; Tumor Cells, Cultured

2003