摘要
目的通过研究丹酚酸A(salvianol acid A,SalA)对肝癌HepG2细胞株c-Met蛋白表达的影响,探讨SalA抑制肝癌细胞增殖,诱导细胞凋亡的可能作用机制。方法以肝癌HepG2细胞株为研究对象,采用MTT法及流式细胞术检测SalA作用后细胞存活、增殖及凋亡情况;同时运用Western blot法及PCR法检测HepG2细胞c-Met及其下游信号通路中关键蛋白和基因表达的改变。结果肝癌HepG2细胞经SalA处理后,其细胞增殖显著抑制,细胞凋亡比例亦升高,且呈浓度依赖性;同时HepG2细胞中c-Met及其下游信号分子AKT的磷酸化水平显著下调,凋亡相关蛋白Bax、caspase-3和caspase-9的表达亦明显上调。结论 SalA能有效抑制肝癌HepG2细胞的增殖并诱导细胞凋亡,其作用机制可能与其抑制HepG2细胞中c-Met蛋白及其下游信号通路中AKT蛋白的磷酸化水平有关。
OBJECTIVE To study the effect of salvianol acid A （SalA） on the protein expression of proto-oncogene c-Met in human hepatocellular carcinoma HepG2 cell line, and explore the potential mechanism of the anti-proliferation and induce-apoptosis effects of SalA on HepG2 cells. METHODS MTT and Flow cytometry methods were used to analyze the anti-proliferation and induce-apoptosis effects of SalA on HepG2 cells. Western blotting and PCR methods were used to analyze the mRNA and protein expression of c-Met and the downstream proteins. RESULTS SalA could effectively inhibit the proliferation of HepG2 cells in vitro, and induce the cell apoptosis. The inhibitory effect was in a dose and incubation time dependent manner. The protein expression and the tyrosine kinase activity of proto-oncogene c-Met and the downstream signal protein AKT were decreased significantly in HepG2 cells after treatment with SalA. The expression of apoptosis-related proteins （Bax, caspase-3 and caspase-9） could also be inhibited significantly. CONCLUSION SalA can inhibit the proliferation of HepG2 cells and the mechanism may be related with inhibiting the activation of proto-oncogene c-Met and the downstream protein AKT, which triggering the cells apoptosis.
出处
《中国现代应用药学》
CAS
CSCD
2014年第5期537-541,共5页
Chinese Journal of Modern Applied Pharmacy
