Ethoxysanguinarine Induces Apoptosis, Inhibits Metastasis and Sensitizes cells to Docetaxel in Breast Cancer Cells through Inhibition of Hakai.
Liang MaXiao-Jing XuanXue-Ming ChenMing-Hui FanJian LiuGuo-Zheng HuangZi LiuPublished in: Chemistry & biodiversity (2023)
Ethoxysanguinarine (ESG) is a benzophenanthridine alkaloid extracted from plants of Papaveraceae family, such as Macleaya cordata (Willd) R. Br. The anti-cancer activity of ESG has been rarely reported. In this study, we investigated the anti-breast cancer effect of ESG and its underlying mechanism. MTT assay and flow cytometry analysis showed that ESG inhibited the viability and induced apoptosis in MCF7 and MDA-MB-231 human breast cancer cells. Western blot revealed that ESG triggered intrinsic and extrinsic apoptotic pathways, as evidenced by the activation of caspase-8, caspase-9 and caspase-3. ESG attenuated breast cancer cell migration and invasion through Hakai/E-cadherin/N-cadherin. Moreover, Hakai knockdown sensitized ESG-triggered viability and motility inhibition, suggesting that Hakai mediated the anti-breast cancer effect of ESG. In addition, ESG potentiated the anti-cancer activity of docetaxel (DTX) in breast cancer cells. Overall, our findings demonstrate that ESG exhibits outstanding pro-apoptosis and anti-metastasis effects on breast cancer via a mechanism related to Hakai-related signaling pathway.
Keyphrases
- induced apoptosis
- breast cancer cells
- endoplasmic reticulum stress
- signaling pathway
- oxidative stress
- cell death
- cell cycle arrest
- flow cytometry
- pi k akt
- epithelial mesenchymal transition
- endothelial cells
- south africa
- squamous cell carcinoma
- single cell
- mass spectrometry
- locally advanced
- staphylococcus aureus
- cystic fibrosis
- drug induced
- breast cancer risk
- rectal cancer
- high resolution
- candida albicans