Song Xu, Yin Zhongqiong, Ye Kuichuan, Wei Qin, Jia Renrong, Zhou Lijun, Du Yonghua, Xu Jiao, Liang Xiaoxia, He Changliang, Shu Gang, Yin Lizi, Lv Cheng
College of Veterinary Medicine, Sichuan Agricultural University Ya-an, 625014, China.
Key Lab of Aromatic Plant Resources Exploitation and Utilization in Sichuan Higher Education, Yibin University Yibin, Sichuan 644000, China.
Int J Clin Exp Pathol. 2014 Apr 15;7(5):2265-72. eCollection 2014.
The aim of this study was to study the anti-hepatoma effect of safrole and elucidate its molecular mechanism, the human hepatoma BEL-7402 cells were incubated with various concentrations (40, 80, 160, 320 and 640 μg/ml) of safrole and the cell proliferation and apoptosis were evaluated. The results showed that both the cell proliferation determined by 3-(4,5-dimethyl-thiazolyl-2)-2,5-diphenyl tetrazolium brominde (MTT) assay and cell colony determined by soft agar assay were significantly suppressed by safrole in a dose-time-dependent manner. Characteristic morphological and biochemical changes associated with apoptosis, including cells shrinkage, deformation and vacuolization of mitochondria, nuclear chromatin condensation and fragmentation, formation of apoptotic bodies were observed when treated with safrole for 24 h and 48 h. Cell cycle changes evaluated by flow cytometry analysis showed that the safrole could induce accumulation of cells arrested at G1 and S phases of the cell cycle. These results demonstrated that safrole is potent anti-hepatoma agent and the underlying mechanism may be attributed to suppress tumor cell growth by inducing cell apoptosis.
本研究旨在探讨黄樟素的抗肝癌作用并阐明其分子机制,用不同浓度(40、80、160、320和640μg/ml)的黄樟素处理人肝癌BEL-7402细胞,评估细胞增殖和凋亡情况。结果显示,通过3-(4,5-二甲基噻唑-2)-2,5-二苯基四氮唑溴盐(MTT)法测定的细胞增殖以及通过软琼脂法测定的细胞集落,均被黄樟素以剂量-时间依赖性方式显著抑制。在用黄樟素处理24小时和48小时后,观察到与凋亡相关的典型形态学和生化变化,包括细胞收缩、线粒体变形和空泡化、核染色质凝聚和碎片化、凋亡小体形成。通过流式细胞术分析评估的细胞周期变化表明,黄樟素可诱导细胞在细胞周期的G1期和S期停滞积累。这些结果表明,黄樟素是一种有效的抗肝癌药物,其潜在机制可能归因于通过诱导细胞凋亡来抑制肿瘤细胞生长。