Inhibition of Sijunzi Decoction extract on human breast cancer cells MDA-MB-468
10.7501/j.issn.0253-2670.2020.04.030
- Author:
Duo-Lu LI
1
Author Information
1. Henan Key Laboratory for Precision Clinical Pharmacy, Department of Pharmacy, The First Affiliated Hospital of Zhengzhou University
- Publication Type:Journal Article
- Keywords:
Apoptosis;
Cell cycle;
Migration;
Proliferation;
Signal transducers and activators of transcription 3;
Sijunzi Decoction;
Triple negative breast cancer
- From:
Chinese Traditional and Herbal Drugs
2020;51(4):1037-1043
- CountryChina
- Language:Chinese
-
Abstract:
Objective: To investigate the effect of Sijunzi Decoction extract (SDE) on the growth of human triple negative breast cancer (TNBC) cell line MDA-MB-468. Methods: MDA-MB-468 cells were treated with different concentrations of SDE. The effect of SDE on the proliferation and migration of the cells were detected by CCK-8 assay and the cell wound healing assay. The colony formation assay was performed to analyze the effect on the ability of colony formation of the cells with SDE. Hoechst 33342 staining technique and flow cytometry (FCM) were used to detect apoptosis and cell cycle of the cells. Western blotting was used to detect the expression levels of STAT3, which was related with the proliferation and apoptosis of cells. Results: Compared with the control group, SDE had a certain inhibitory effect on MDA-MB-468 cells (P < 0.05), and it was dependent on the concentration and time. Cloning formation experiments showed that SDE inhibited the clonality of the cells. The cell migration experiment showed that the wound healing ability of the cells could be weakened by the extract with the medium and high dosage (P < 0.001). The results of FCM showed that the apoptosis rate of all SDE dosage increased gradually in a dose-dependent manner. And SDE with the medium and high dosage induced apoptosis of the cells significantly (P < 0.01 and 0.001). Cell cycle was affected by SDE with the obvious reduction of the cells in G2 phase (P < 0.01). The results of Western blotting showed that the expression level of STAT3 was decreased significantly. Conclusion: SDE inhibited the proliferation and clonal formation of MDA-MB-468 cells, inhibited migration, promoted apoptosis and decreased the cells of G2 phase. which may be related to the regulation of STAT3 pathway.
