Einbond Linda Saxe, Shimizu Masahito, Xiao Danhua, Nuntanakorn Paiboon, Lim Jin T E, Suzui Masumi, Seter Colette, Pertel Thomas, Kennelly Edward J, Kronenberg Fredi, Weinstein I Bernard
Herbert Irvign Comperhensive Cancer Center, Columbia University College of Physicians and Surgeons, New York, NY 10032, USA.
Breast Cancer Res Treat. 2004 Feb;83(3):221-31. doi: 10.1023/B:BREA.0000014043.56230.a3.
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 micro g/ml, respectively. It also induced cell cycle arrest at G1 when tested at 30 micro g/ml and at G2/M at 60 micro g/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 p21cip1 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.
本研究的目的是确定黑升麻是否含有抑制人乳腺癌细胞生长的成分,因此最终可能有助于预防或治疗乳腺癌。用甲醇/水提取黑升麻根茎,并通过溶剂-溶剂分配进行分级分离,得到三个级分:己烷、乙酸乙酯和水。乙酸乙酯级分在基于细胞的两种分析方法(生长抑制和细胞周期分析)中显示出最高效力。该级分抑制ER+ MCF7和ER- MDA-MB-453人乳腺癌细胞系的生长,IC50值分别约为20和10微克/毫升。在MCF7细胞中,当以30微克/毫升测试时,它还诱导细胞周期在G1期停滞,以60微克/毫升测试时在G2/M期停滞。这表明提取物含有多种成分的混合物,其中活性较高(或含量较高)的成分导致G1期停滞,活性较低的成分导致G2/M期停滞。然后我们检查了该提取物中的特定成分。通过聚酰胺柱色谱获得的三萜糖苷级分,以及特定的三萜糖苷actein、23-表-26-脱氧actein和升麻酰胺A,抑制MCF7人乳腺癌细胞的生长并诱导细胞周期在G1期停滞。最有效的化合物actein降低了MCF7细胞中细胞周期蛋白D1、细胞周期蛋白依赖性激酶4和pRb蛋白的过度磷酸化形式的水平,并增加了p21cip1的水平,这些变化可能有助于细胞停滞在G1期。目前正在进行进一步的研究,以确定黑升麻中存在的actein和相关化合物抑制人乳腺癌细胞生长的机制。