Wu Yi-Feng, Cao Ming-Fu, Gao Yan-Ping, Chen Fei, Wang Tao, Zumbika Edward P, Qian Kai-Xian
College of Life Sciences, Zhejiang University, Hangzhou 310027, Zhejiang Province, China.
World J Gastroenterol. 2004 Oct 15;10(20):2944-8. doi: 10.3748/wjg.v10.i20.2944.
To investigate the effect of schisandrin B (Sch B) on proliferation and apoptosis of human hepatoma SMMC-7721 cells in vitro and regulation of Hsp70 and Caspases-3, 7, 9 expression by Sch B.
Human hepatoma cell line SMMC-7721 was cultured and treated with Sch B at various concentrations. Growth suppression was detected with MTT colorimetric assay. Cell apoptosis was confirmed by DNA ladder detection and flow cytometric analysis. The expression of Hsp70, Caspases-3, 7, 9 were analyzed by Western blot analysis.
Sch B inhibited the growth of hepatoma SMMC-7721 cells in a dose-dependent manner, leading to a 50% decrease in cell number (LC50) value of 23.50 mg/L. Treatment with Sch B resulted in degradation of chromosomal DNA into small internucleosomal fragments, evidenced by the formation of a 180-200 bp DNA ladder on agarose gels. FCM analysis showed the peak areas of subdiploid at the increased concentration of Sch B. The results of Western bolt analysis showed that Hsp70 was down-regulated and Caspase-3 was up-regulated, while the activity of Caspases-7, -9 had no significant change.
Sch B is able to inhibit the proliferation of human hepatoma SMMC-7721 cells and induce apoptosis, which goes through Caspase-3-dependent and Caspase-9-independent pathway accompanied with the down-regulation of Hsp70 protein expression at an early event.
研究五味子乙素(Sch B)对人肝癌SMMC-7721细胞体外增殖和凋亡的影响以及Sch B对热休克蛋白70(Hsp70)和半胱天冬酶-3、-7、-9表达的调控作用。
培养人肝癌细胞系SMMC-7721,并用不同浓度的Sch B进行处理。采用MTT比色法检测生长抑制情况。通过DNA梯状条带检测和流式细胞术分析确认细胞凋亡。采用蛋白质免疫印迹法分析Hsp70、半胱天冬酶-3、-7、-9的表达。
Sch B以剂量依赖性方式抑制肝癌SMMC-7721细胞的生长,使细胞数量减少50%的浓度(LC50)值为23.50 mg/L。Sch B处理导致染色体DNA降解为小的核小体间片段,琼脂糖凝胶上形成180 - 200 bp的DNA梯状条带可证明这一点。流式细胞术分析显示,随着Sch B浓度增加,亚二倍体峰面积增大。蛋白质免疫印迹分析结果显示,Hsp70表达下调,半胱天冬酶-3表达上调,而半胱天冬酶-7、-9的活性无显著变化。
Sch B能够抑制人肝癌SMMC-7721细胞的增殖并诱导凋亡,其凋亡途径为依赖半胱天冬酶-3且不依赖半胱天冬酶-9的途径,且早期伴有Hsp70蛋白表达下调。