[6]-Gingerol induces Caspase-Dependent Apoptosis in Bladder Cancer cells via MAPK and ROS Signaling

被引:11
作者
Choi, Na Ri [1 ]
Choi, Woo-gyun [1 ]
Kwon, Min Ji [1 ]
Woo, Joo Han [2 ,3 ]
Kim, Byung Joo [1 ]
机构
[1] Pusan Natl Univ, Div Longev & Biofunct Med, Sch Korean Med, 49 Busandaehakro, Yangsan 50612, South Korea
[2] Dongguk Univ, Dept Physiol, Coll Med, Gyeongju 38066, South Korea
[3] Dongguk Univ, Coll Med, Channelopathy Res Ctr CRC, 32 Dongguk Ro, Goyang 10326, Gyeonggi Do, South Korea
基金
新加坡国家研究基金会;
关键词
6]-gingerol; cell proliferation; apoptosis; bladder cancer; 5637; POTENTIAL MELASTATIN 7; TRP CHANNELS; TUMOR-GROWTH; MIGRATION; INHIBITION; GINGER; PROLIFERATION; INVASION; PATHWAYS; DEATH;
D O I
10.7150/ijms.73077
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The anti-cancer effects of [6]-gingerol ([6]-GIN), the main active polyphenol of ginger (Zingiber officinale), were investigated in the human bladder cancer cell line 5637. [6]-GIN inhibited cell proliferation, increased sub-G1 phase ratios, and depolarized mitochondrial membrane potential. [6]-GIN-induced cell death was associated with the downregulation of B-cell lymphoma 2 (BCL-2) and survivin and the upregulation of Bcl-2-associated X protein (Bax). [6]-GIN activated caspase-3 and caspase-9 and regulated the activation of mitogen-activated protein kinases (MAPKs). Further, [6]-GIN also increased the intracellular reactive oxygen species (ROS) levels and TG100-115 or tranilast increased [6]-GIN-induced cell death. These results suggest that [6]-GIN induced apoptosis in the bladder cancer cell line 5637 and therefore has the potential to be used in the development of new drugs for bladder cancer treatment.
引用
收藏
页码:1093 / 1102
页数:10
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