Estrogenic activity of osthole and imperatorin in MCF-7 cells and their osteoblastic effects in Saos-2 cells

被引:0
作者
Jia Min [1 ]
Li Yuan [1 ]
Xin Hai-Liang [1 ]
Hou Ting-Ting [1 ]
Zhang Nai-Dai [1 ]
Xu Hong-Tao [1 ]
Zhang Qiao-Yan [1 ]
Qin Lu-Ping [1 ]
机构
[1] Second Mil Med Univ, Sch Pharm, Dept Pharmacognosy, Shanghai 200433, Peoples R China
基金
中国国家自然科学基金;
关键词
Osthole; Imperatorin; MCF-7; Estrogenic activity; Estrogen receptors; Osteoblasts; Alkaline phosphatase; BREAST-CANCER CELLS; GENE-EXPRESSION; CNIDIUM-MONNIERI; RECEPTOR-ALPHA; MAP KINASE; ESTRADIOL; DIFFERENTIATION; PATHWAY; PHYTOESTROGENS; PROLIFERATION;
D O I
暂无
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
There is an increasing interest in phytoestrogens due to their potential medical usage in hormone replacement therapy (HRT). The present study was designed to investigate the in vitro effects of estrogen-like activities of two widespread coumarins, osthole and imperatorin, using the MCF-7 cell proliferation assay and their alkaline phosphatase (ALP) activities in osteoblasts Saos-2 cells. The two compounds were found to strongly stimulate the proliferation of MCF-7 cells. The estrogen receptor-regulated ER alpha, progesterone receptor (PR) and PS2 mRNA levels were increased by treatment with osthole and imperatorin. All these effects were significantly inhibited by the specific estrogen receptor antagonist ICI182, 780. Cell cycle analysis revealed that their proliferation stimulatory effect was associated with a marked increase in the number of MCF-7 cells in S phase, which was similar to that observed with estradiol. It was also observed that they significantly increased ALP activity, which was reversed by ICI182,780. These results suggested that osthole and imperatorin could stimulate osteoblastic activity by displaying estrogenic properties or through the ER pathway. In conclusion, osthole and imperatorin may represent new pharmacological tools for the treatment of osteoporosis.
引用
收藏
页码:413 / 420
页数:8
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