Realgar transforming solution displays anticancer potential against human hepatocellular carcinoma HepG2 cells by inducing ROS

被引:32
作者
Song, Peng [1 ]
Chen, Peng [2 ]
Wang, Dong [1 ]
Wu, Zhengrong [2 ]
Gao, Qiyu [1 ]
Wang, Aixia [2 ]
Zhu, Ruilan [2 ]
Wang, Yajun [1 ]
Wang, Xin [2 ]
Zhao, Longhe [2 ]
Duan, Ziyun [2 ]
Zhu, Shuqian [2 ]
Cui, Peng [2 ]
Li, Yang [2 ]
Li, Hongyu [1 ,2 ]
机构
[1] Lanzhou Univ, Sch Life Sci, Inst Microbiol, 222 Tianshui Rd, Lanzhou 730000, Gansu, Peoples R China
[2] Lanzhou Univ, Sch Pharm, Lanzhou 730020, Gansu, Peoples R China
基金
中国国家自然科学基金;
关键词
realgar transforming solution; HepG2; cell; reactive oxygen species; cell cycle arrest; apoptosis; CYCLE CHECKPOINTS; BIOLEACHING SOLUTION; ARSENIC TRIOXIDE; P53; APOPTOSIS; LEUKEMIA; CANCER; MITOCHONDRIA; PATHWAY; TRANSLOCATION;
D O I
10.3892/ijo.2016.3831
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Realgar (As4S4), as a mineral drug containing arsenic compound, has been employed in clinical therapy of cancer for its good therapeutic reputation in Chinese traditional medicine. However, large dose of realgar and long period of treatment are necessary for achieving the effective blood medicine concentration due to its low bioavailability resulted from poor solubility. In this study, we obtained realgar transforming solution (RTS) using intrinsic biotransformation in microorganism, and investigated underlying mechanisms of RTS for HepG2 cells. Our results demonstrated that an effective biotransformation of realgar method by A. ferrooxidans was established, in which realgar was biologically converted into an aqueous solution, and RTS had a strong activity inducing apoptosis and interrupting G2/M progression in HepG2 cells via upregulation of cellular ROS. Importantly, RTS inhibited the cellular antioxidant defense system leading to abundant ROS accumulation, and activated cell cycle arrest and mitochondrial pathway of apoptosis mediated by activating p53 due to cellular uncontrolled ROS. Collectively, our findings suggest that RTS is a potential candidate for therapy of human hepatocellular carcinoma.
引用
收藏
页码:660 / 670
页数:11
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