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World J Gastroenterol. Jul 21, 2010; 16(27): 3385-3393
Published online Jul 21, 2010. doi: 10.3748/wjg.v16.i27.3385
Published online Jul 21, 2010. doi: 10.3748/wjg.v16.i27.3385
Figure 6 Effect of N-acetylcysteine, an antioxidant, and GW9662, a blocker of peroxisome proliferator-activated receptor-γ, and Jun N-terminal kinase inhibitor SP600125 on 8-bromo-7-methoxychrysin-induced activation of Jun N-terminal kinase (A), apoptosis (B), activation of caspase-3 (C), and DNA fragmentation (D) in HepG2 cells.
The ratio of p-Jun N-terminal kinase (JNK)/JNK or p-c-Jun/c-Jun was normalized to 0 h or the untreated group. aP < 0.05 vs treatment with dimethyl sulfoxide (DMSO); cP < 0.05 vs treatment with 8-bromo-7-methoxychrysin (BrMC) alone; eP < 0.05 vs treatment with N-acetylcysteine (NAC) in combination with SP600125 and BrMC or GW9662 in combination with SP600125 and BrMC.
- Citation: Yang XH, Zheng X, Cao JG, Xiang HL, Liu F, Lv Y. 8-bromo-7-methoxychrysin-induced apoptosis of hepatocellular carcinoma cells involves ROS and JNK. World J Gastroenterol 2010; 16(27): 3385-3393
- URL: https://www.wjgnet.com/1007-9327/full/v16/i27/3385.htm
- DOI: https://dx.doi.org/10.3748/wjg.v16.i27.3385