Ginger ingredients reduce viability of gastric cancer cells via distinct mechanisms

被引:130
作者
Ishiguro, Kazuhiro
Ando, Takafumi
Maeda, Osamu
Ohmiya, Naoki
Niwa, Yasumasa
Kadomatsu, Kenji
Goto, Hidemi
机构
[1] Nagoya Univ, Sch Med, Showa Ku, Nagoya, Aichi 4668550, Japan
[2] Nagoya Univ, Sch Med, Dept Gastroenterol, Showa Ku, Nagoya, Aichi 4668550, Japan
[3] Nagoya Univ, Sch Med, Dept Biochem, Showa Ku, Nagoya, Aichi 4668550, Japan
关键词
herbal medicine; stomach neoplasms; TRAIL; NF-kappa B; microtubules;
D O I
10.1016/j.bbrc.2007.08.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Ginger has been used throughout the world as spice, food and traditional herb. We found that 6-gingerol, a phenolic alkanone isolated from ginger, enhanced the TRAIL-induced viability reduction of gastric cancer cells while 6-gingerol alone affected viability only slightly. 6-Gingerol facilitated TRAIL-induced apoptosis by increasing TRAIL-induced caspase-3/7 activation. 6-Gingerol was shown to down-regulate the expression of cIAPI, which suppresses caspase-3/7 activity, by inhibiting TRAIL-induced NF-kappa B activation. As 6-shogaol has a chemical structure similar to 6-gingerol, we also assessed the effect of 6-shogaol on the viability of gastric cancer cells. Unlike 6-gingerol, 6-shogaol alone reduced the viability of gastric cancer cells. 6-Shogaol was shown to damage microtubules and induce mitotic arrest. These findings indicate for the first time that in gastric cancer cells, 6-gingerol enhances TRAIL-induced viability reduction by inhibiting TRAIL-induced NF-kappa B activation while 6-shogaol alone reduces viability by damaging microtubules. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:218 / 223
页数:6
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