The Cytotoxicity of Kahweol in HT-29 Human Colorectal Cancer Cells Is Mediated by Apoptosis and Suppression of Heat Shock Protein 70 Expression

被引:46
|
作者
Choi, Dong Wook [1 ]
Lim, Man Sup [2 ,3 ]
Lee, Jae Won [2 ]
Chun, Wanjoo [2 ]
Lee, Sang Hyuk
Nam, Yang Hoon [1 ]
Park, Jin Myung [1 ]
Choi, Dae Hee [1 ]
Kang, Chang Don [1 ]
Lee, Sung Joon [1 ]
Park, Sung Chul [1 ]
机构
[1] Kangwon Natl Univ, Sch Med, Dept Internal Med, Chunchon 701200, South Korea
[2] Kangwon Natl Univ, Sch Med, Dept Pharmacol, Chunchon 701200, South Korea
[3] Hallym Univ, Sacred Heart Hosp, Dept Surg, Anyang 431796, South Korea
关键词
Kahweol; Apoptosis; Heat shock protein 70; Colorectal cancer; HEAT-SHOCK PROTEINS; COLON-CANCER; COFFEE CONSUMPTION; HSP70; METAANALYSIS; CAFESTOL; RISK; DITERPENES; GROWTH; DEATH;
D O I
10.4062/biomolther.2014.133
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Although coffee is known to have antioxidant, anti-inflammatory, and antitumor properties, there have been few reports about the effect and mechanism of coffee compounds in colorectal cancer. Heat shock proteins (HSPs) are molecular chaperones that prevent cell death. Their expression is significantly elevated in many tumors and is accompanied by increased cell proliferation, metastasis and poor response to chemotherapy. In this study, we investigated the cytotoxicity of four bioactive compounds in coffee, namely, caffeine, caffeic acid, chlorogenic acid, and kahweol, in HT-29 human colon adenocarcinoma cells. Only kahweol showed significant cytotoxicity. Specifically, kahweol increased the expression of caspase-3, a pro-apoptotic factor, and decreased the expression of anti-apoptotic factors, such as BcI-2 and phosphorylated Akt. In addition, kahweol significantly attenuated the expression of HSP70. Inhibition of HSP70 activity with triptolide increased kahweol-induced cytotoxicity. In contrast, overexpression of HSP70 significantly reduced kahweol-induced cell death. Taken together, these results demonstrate that kahweol inhibits colorectal tumor cell growth by promoting apoptosis and suppressing HSP70 expression.
引用
收藏
页码:128 / 133
页数:6
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