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Betulin induces reactive oxygen species-dependent apoptosis in human gastric cancer SGC7901 cells
- Li, Yang, Liu, Xiaokang, Jiang, Dan, Lin, Yingjia, Wang, Yushi, Li, Qing, Liu, Linlin, Jin, Ying-Hua
- Archives of pharmacal research 2016 v.39 no.9 pp. 1257-1265
- acetylcysteine, antioxidants, apoptosis, betulin, caspases, cell viability, dose response, humans, mitochondria, oxygen, proteins, reactive oxygen species, stomach neoplasms
- Betulin, an abundant natural compound, significantly inhibited the cell viability of advanced human gastric cancer SGC7901 cells. Mechanism study demonstrated that betulin induced apoptosis through mitochondrial Bax and Bak accumulation-mediated intrinsic apoptosis pathway. Downregulation of the anti-apoptosis proteins Bcl-2 and XIAP was involved during betulin-induced cell apoptosis. Reactive oxygen species (ROS) was generated in cells after betulin treatment in a time- and dose-dependent manner. Addition of antioxidant N-acetyl-L-cysteine (NAC) significantly attenuated betulin-induced ROS generation as well as Bcl-2 and XIAP downregulation. The mitochondrial accumulation of Bax and Bak, as well as caspase activity, was also remarkably inhibited by NAC treatment, indicating that ROS are important signaling intermediates that lead to betulin-induced apoptosis by modulating multiple apoptosis-regulating proteins in SGC7901 cells.