WANG Hai-bo, NI Teng-yang, FENG Jun, et al. Effect of Extract in Inhibiting Metastasis of Gastric Cancer BGC-823 Cells via Cofilin1[J]. Chinese journal of experimental traditional medical formulae, 2018, 24(19): 112-116.
WANG Hai-bo, NI Teng-yang, FENG Jun, et al. Effect of Extract in Inhibiting Metastasis of Gastric Cancer BGC-823 Cells via Cofilin1[J]. Chinese journal of experimental traditional medical formulae, 2018, 24(19): 112-116. DOI: 10.13422/j.cnki.syfjx.20181921.
Objective: To explore the role and mechanism of Celastrus orbiculatus extract (COE) in inhibiting the metastasis of gastric cancer
in order to seek new targets in preventing and treating gastric cancer with traditional Chinese medicine and lay a theoretical and experimental foundation for the development of effective anti-gastric cancer drugs are very important. Method: According to the results of the previous two-dimensional electrophoresis experiment
the differentially expressed target proteins of COE (20
40
80 mg·L-1) in gastric cancer were screened out. Then the expression of Cofilin 1 (CFL1) in the gastric cancer cells after COE intervention was detected by Western blot. Finally
the molecular cloning technique was used to inhibit the expression of CFL1 in gastric cancer BGC-823 cells
then COE was used to detect whether it could affect the metastasis of gastric cancer cells. Result: CFL1 was stably overexpressed in gastric cancer cells based on previous experiments. Western blot results showed that COE inhibited the expression of CFL1(P<0.01). Various concentrations of COE (20
40
80 mg·L-1) inhibited the expression of CFL1 in BGC-823 cells. And the expression of CFL1 was significantly inhibited by small interfering RNA (siRNA)(P<0.01). The transwell experiments showed that COE markedly reduced the number of transmembrane cells in low expressed BGC823 cells
with statistically significant differences(P<0.01). Conclusion: COE could significantly inhibit the metastasis of gastric cancer BGC-823 cells
and its mechanism may be related to the inhibition of overexpression of CFL1.