Extract from Astragalus membranaceus inhibit breast cancer cells proliferation via PI3K/AKT/mTOR signaling pathway

被引:132
作者
Zhou, Ruijuan [1 ]
Chen, Hongjiu [1 ]
Chen, Junpeng [1 ]
Chen, Xuemei [2 ]
Wen, Yu [2 ]
Xu, Leqin [3 ]
机构
[1] Fujian Univ Tradit Chinese Med, Xiamen Hosp Tradit Chinese Med, Dept Chest & Breast Surg, 1739 Xianyue Rd, Xiamen 361009, Peoples R China
[2] Fujian Univ Tradit Chinese Med, Xiamen Hosp Tradit Chinese Med, Dept Pharm, 1739 Xianyue Rd, Xiamen 361009, Peoples R China
[3] Fujian Univ Tradit Chinese Med, Xiamen Hosp Tradit Chinese Med, Dept Sci & Educ, 1739 Xianyue Rd, Xiamen 361009, Peoples R China
来源
BMC COMPLEMENTARY AND ALTERNATIVE MEDICINE | 2018年 / 18卷
基金
中国国家自然科学基金;
关键词
Astragalus membranaceus; Extract; Breast cancer; Apoptosis; PI3K; AKT; LUNG-CANCER; CARCINOMA-CELLS; IN-VITRO; APOPTOSIS; FORMONONETIN; POLYSACCHARIDES; EXPRESSION;
D O I
10.1186/s12906-018-2148-2
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Background: Astragalus membranaceus (AM) is a commonly used herb in traditional Chinese medicine (TCM), which has been used as an essential tonic to treat various diseases for more than 2000 years. In this study, we aimed to investigate the biological effects of extract from AM on breast cancer cell and its mechanism. Methods: To prepare the extract, dried AM were ground and extracted with water extraction-ethanol supernatant method. Then the main isoflavones in the extract was detect by HPLC analysis. Furthermore, the anti-proliferative activity of AM extract was examined by MTT assay and morphological observation. Cell apoptosis was evaluated with flow cytometric analysis. The expressions of total and phosphorylated PI3K, GS3K beta, Akt and mTOR were determined by western blot analysis. Results: HPLC analysis demonstrated that AM extract contained with four kinds of isoflavones, campanulin, ononin, calycosin and formononetin. The MTT test and morphological observation indicated that cells proliferation of MCF-7, SK-BR-3 and MDA-MB-231 were inhibited by AM extract in a dose dependent manner. Furthermore, flow cytometric analysis displayed that after treated with 25 mu g/ml and 50 mu g/ml AM extract, apoptosis of breast cancer cells was significantly increased as compared with DMSO and blank control group (all p < 0.05). Western blot analysis found that the level of p-PI3K, p-GS3K beta, p-Akt, and p-mTOR were significantly decreased, but the level of total-mTOR was observably increased as compared with DMSO control group. Conclusions: Taken together, the inhibited cell proliferation and induced cell apoptosis effect of AM extract via PI3K/AKT/mTOR pathway confirmed the anti-tumor potential of AM. Therefore, our findings provide a new insight into anti-cancer effect of AM extract as a promising agent in breast cancer treatment.
引用
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页数:8
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