Esculetin enhances TRAIL-induced apoptosis through DR5 upregulation in human oral cancer SAS cells

被引:55
|
作者
Kok, Sang-Heng [2 ]
Yeh, Cheng-Chang [2 ]
Chen, Mei-Ling [2 ]
Kuo, Mark Yen-Ping [1 ,2 ]
机构
[1] Natl Taiwan Univ Hosp, Sch Dent, Dept Dent, Taipei 10016, Taiwan
[2] Natl Taiwan Univ, Sch Dent, Coll Med, Taipei 10764, Taiwan
关键词
DR5; Esculetin; Oral cancer; TRAIL; Chemotherapy; EXPRESSION; CARCINOMA; HEAD; INDUCTION; THERAPEUTICS; LIPOXYGENASE; CHEMOTHERAPY; PROGRESSION; SUPEROXIDE; INHIBITION;
D O I
10.1016/j.oraloncology.2009.07.018
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Esculetin has been shown to selectively induce tumor apoptosis in several types of cancers and is regarded as a promising chemotherapeutic agent. In this study, we showed that esculetin significantly suppressed the growth of oral cancer SAS cells in a dose-dependent manner. DNA content flow cytometry and TUNEL assay revealed that esculetin induced cell cycle arrest and apoptosis. Western blotting showed esculetin increased DR5 protein expression and activated caspase-8, which differed from previous studies conducted in other cell types. Furthermore, treatment with esculetin significantly increased TRAIL-induced apoptosis in SAS cells and the TRAIL-sensitizing effect was blocked by DR5/Fc chimera protein. Our results indicate that esculetin enhances TRAIL-induced apoptosis primarily through upregulation of DR5. Combination of esculetin and TRAIL may be a novel treatment strategy for oral cancers. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1067 / 1072
页数:6
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