Activity of the antiestrogenic cajanin stilbene acid towards breast cancer

作者：Fu Yujie; Kadioglu Onat; Wiench Benjamin; Wei Zuofu; Wang Wei; Luo Meng; Yang Xiaohe; Gu Chengbo; Zu Yuangang; Efferth Thomas^*

来源：Journal of Nutritional Biochemistry, 2015, 26(11): 1273-1282.

DOI：10.1016/j.jnutbio.2015.06.004

• Breast cancer
• Estrogen receptor
• Microarray
• Pharmacogenomics
• Tamoxifen resistance
• Xenograft tumor

Antiestrogenic therapy is a mainstay for estrogen receptor (ER alpha)-positive breast cancer. Due to the development of resistance to established antihormones such as tamoxifen, novel compounds are required. The low abundant cajanin stilbene acid (CSA) recently isolated by us from Pigeon Pea (Cajanus cajan) has structural similarities with estrogen. We analyzed the cytotoxic and anticancer activity of CSA in ER alpha-positive and -negative human breast cancer cells in vitro, in vivo and in silico. CSA exerts anticancer and antiestrogenic activities towards ER alpha-positive breast cancer, and it showed cytotoxicity towards tamoxifen-resistant MCF-7 cells, implying that CSA may be active against tamoxifen-resistant breast cancer cells. CSA showed low cytotoxicity in ER alpha-negative breast tumor cells as expected. Comparable cytotoxicity was observed towards p53 negative MCF-7 cells, implying that CSA is effective independent of the p53 status. Xenografted MCF-7 cells in nude mice were better inhibited by CSA than by cyclophosphamide. Testing of 8 primary cell cultures derived from human breast cancer biopsies showed that cell cultures from ER-positive tumors were more sensitive than from ER-negative ones. Dose-dependent decrease in ER alpha protein levels was observed upon CSA treatment. Synergistic effect with tamoxifen was observed in terms of increased p53 protein level. CSA affected pathways related to p53, cancer and cell proliferation. Gene promoter analyses supported the ER alpha regulation. CSA bound to the same site as 17 beta-estradiol and tamoxifen on ER alpha. In conclusion, CSA exerts its anticancer effects in ER alpha-positive breast cancer cells by binding and inhibiting ER alpha.

• 出版日期2015-11
• 单位东北林业大学