Ye Liang-Fei, Wang Yi-Qi, Yang Bo, Zhang Ru-Song
Department of Pharmacy, Zhejiang Chinese Medical University, Hangzhou 310053, P.R. China.
Oncol Lett. 2013 Apr;5(4):1407-1411. doi: 10.3892/ol.2013.1186. Epub 2013 Feb 7.
The present study aimed to investigate the anti-cancer effect of a C-steroidal glycoside (CG) isolated from the roots of . CG was able to inhibit the growth of human cancer cells (SGC-7901 cells) in a concentration and time-dependent manner . SGC-7901 cells exposed to CG (10.8 and 21.6 M) exhibited typical morphological apoptosis characteristics, such as nuclear-chromatin condensation and apoptotic body formation. Flow cytometric analysis showed that after treatment with CG at 10.8 and 21.6 M for 24 h, the percentage of apoptotic cells increased to 30.4 and 43.2%, respectively, while the number of cells in the G/G, S and G/M phases of the cell cycle decreased (P<0.05). Furthermore, treatment with CG at a concentration of 21.6 M for 24 h significantly increased the expression of caspase-3 and the activity of caspase-3 was increased ∼3-fold in SGC-7901 cells. These results suggest that CG is the active anticancer component of the total C-glycosides of the roots of which is able to inhibit the growth of cancer cells and induce cancer cell apoptosis through caspase-3-dependent pathways.
本研究旨在探讨从[植物名称]根部分离出的一种C-甾体糖苷(CG)的抗癌作用。CG能够以浓度和时间依赖性方式抑制人癌细胞(SGC-7901细胞)的生长。暴露于CG(10.8和21.6 μM)的SGC-7901细胞表现出典型的形态学凋亡特征,如核染色质浓缩和凋亡小体形成。流式细胞术分析表明,用10.8和21.6 μM的CG处理24小时后,凋亡细胞的百分比分别增加到30.4%和43.2%,而细胞周期G0/G1、S和G2/M期的细胞数量减少(P<0.05)。此外,用21.6 μM的CG处理24小时显著增加了SGC-7901细胞中caspase-3的表达,且caspase-3的活性增加了约3倍。这些结果表明,CG是[植物名称]根中总C-糖苷的活性抗癌成分,能够通过caspase-3依赖性途径抑制癌细胞生长并诱导癌细胞凋亡。