小檗碱
黄连
Wnt信号通路
癌症研究
细胞凋亡
细胞周期
细胞生长
转移
乳腺癌
癌细胞
上皮-间质转换
信号转导
连环素
化学
生物
癌症
药理学
医学
内科学
细胞生物学
病理
生物化学
中医药
替代医学
作者
Lu-lu Dian,Zhaozhen Xu,Yanfang Sun,Jinhua Li,Hongfei Lu,Meng Zheng,Juan Wang,Л. Б. Дробот,I. R. Horak
出处
期刊:Phytochemistry
[Elsevier]
日期:2022-08-01
卷期号:200: 113217-113217
被引量:24
标识
DOI:10.1016/j.phytochem.2022.113217
摘要
Berberine alkaloids belong to the class of isoquinoline alkaloids that have been shown to possess anticancer potential, berberine exhibits inhibitory effects on breast cancer development. However, the exact mechanisms of action for anti-breast carcinoma of the alkaloids, including epiberberine, berberrubine and dihydroberberine are still unclear. MTT assay, colony formation, wound healing and transwell invasion assays detected these alkaloids suppressed proliferation, migration and invasion of breast cancer cells. Hoechst and Annexin V-FITC/PI staining were used to analyze the apoptosis of breast cancer cells. Western blotting investigated the changes noted in the expression levels of the key proteins involved in the Wnt/β-catenin signaling pathway and epithelial to mesenchymal transition (EMT). The results showed that inhibited the proliferation of breast cancer cells. Berberine alkaloids inhibited the cell cycle at G2/M phase in MCF-7 cells, but in MDA-MB-231 cells berberine alkaloids arrested the cell cycle in G0/G1 and G2/M phases. By decreasing β-catenin expression, increasing GSK-3β expression and decreasing N-cadherin expression, increasing E-cadherin expression, which proved that epiberberine, berberrubine and dihydroberberine inhibited of metastasis of breast cancer cells through Wnt signaling pathway and reversed EMT except berberine. Furthermore, berberine alkaloids exert their anti-breast cancer effects through the synergistic action of intrinsic and extrinsic pathways of apoptosis. These findings highlight the different effects of different berberine alkaloids on breast cancer cells and confirm that berberine alkaloids may be potentially used in the treatment of breast cancer.
科研通智能强力驱动
Strongly Powered by AbleSci AI