4.5 Article

Growth inhibitory activity of extracts and purified components of black cohosh on human breast cancer cells

期刊

BREAST CANCER RESEARCH AND TREATMENT
卷 83, 期 3, 页码 221-231

出版社

SPRINGER
DOI: 10.1023/B:BREA.0000014043.56230.a3

关键词

Actaea racemosa; actein; Cimicifuga racemosa; cinnamic acid ester; cyclin D1; triterpene glycoside

类别

资金

  1. NCCIH NIH HHS [3P50AT00090-02S2] Funding Source: Medline

向作者/读者索取更多资源

The purpose of this study was to determine whether black cohosh contains constituents that inhibit the growth of human breast cancer cells, and therefore might eventually be useful in the prevention or treatment of breast cancer. Black cohosh rhizomes were extracted with methanol/water and fractionated by solvent-solvent partitioning to yield three fractions: hexane, ethyl acetate and water. The ethyl acetate fraction displayed the highest potency in two cell-based assays, growth inhibition and cell cycle analysis. This fraction inhibited growth of both the ER+ MCF7 and ER(-)MDA-MB-453 human breast cancer cell lines with IC50 values of about 20 and 10 mug/ml, respectively. It also induced cell cycle arrest at G1 when tested at 30 mug/ml and at G2/M at 60 mug/ml in MCF7 cells. This suggests that the extract contains a mixture of components with the more active (or more abundant) causing G1 arrest and the less active causing G2/M arrest. We then examined specific components in this extract. The triterpene glycoside fraction obtained by polyamide column chromatography, and the specific triterpene glycosides actein, 23-epi-26-deoxyactein and cimiracemoside A, inhibited growth of the MCF7 human breast cancer cells and induced cell cycle arrest at G1. The most potent compound, actein, decreased the level of cyclin D1, cdk4 and the hyperphosphorylated form of the pRb protein and increased the level of p21(cip1) in MCF7 cells, changes that may contribute to the arrest in G1. Further studies are in progress to identify the mechanisms by which actein and related compounds present in black cohosh inhibit growth of human breast cancer cells.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据