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
相关论文
共 40 条
[1]  
[Anonymous], ANN ONCOL S6
[2]   Safety and antitumor activity of recombinant soluble Apo2 ligand [J].
Ashkenazi, A ;
Pai, RC ;
Fong, S ;
Leung, S ;
Lawrence, DA ;
Masters, SA ;
Blackie, C ;
Chang, L ;
McMurtrey, AE ;
Hebert, A ;
DeForge, L ;
Koumenis, IL ;
Lewis, D ;
Harris, L ;
Bussiere, J ;
Koeppen, H ;
Shahrokh, Z ;
Schwall, RH .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 104 (02) :155-162
[3]   Neoadjuvant chemotherapy for locally advanced squamous cancers of the head and neck: current status and future prospects [J].
Chandana, Sreenivasa R. ;
Conley, Barbara A. .
CURRENT OPINION IN ONCOLOGY, 2009, 21 (03) :218-223
[4]   Superoxide anion scavenging effect of coumarins [J].
Chang, WS ;
Lin, CC ;
Chuang, SC ;
Chiang, HC .
AMERICAN JOURNAL OF CHINESE MEDICINE, 1996, 24 (01) :11-17
[5]   Induction of apoptosis by esculetin in human leukemia cells [J].
Chu, CY ;
Tsai, YY ;
Wang, CJ ;
Lin, WL ;
Tseng, TH .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2001, 416 (1-2) :25-32
[6]   New options in the treatment of locally advanced head and neck cancer:: Role for induction chemotherapy [J].
Cruz, Juan J. ;
Ocana, Alberto ;
Navarro, Miguel ;
Del Barco, Elvira ;
Fonseca, Emilio .
CANCER TREATMENT REVIEWS, 2008, 34 (03) :268-274
[7]  
Fukuda M, 2003, ONCOL REP, V10, P1113
[8]   Cancer Statistics, 2009 [J].
Jemal, Ahmedin ;
Siegel, Rebecca ;
Ward, Elizabeth ;
Hao, Yongping ;
Xu, Jiaquan ;
Thun, Michael J. .
CA-A CANCER JOURNAL FOR CLINICIANS, 2009, 59 (04) :225-249
[9]   Role of the TRAIL/APO2-L death receptors in chlorambucil- and fludarabine-induced apoptosis in chronic lymphocytic leukemia [J].
Johnston, JB ;
Kabore, AF ;
Strutinsky, J ;
Hu, XJ ;
Paul, JT ;
Kropp, DM ;
Kuschak, B ;
Begleiter, A ;
Gibson, SB .
ONCOGENE, 2003, 22 (51) :8356-8369
[10]   The TRAIL apoptotic pathway in cancer onset, progression and therapy [J].
Johnstone, Ricky W. ;
Frew, Ailsa J. ;
Smyth, Mark J. .
NATURE REVIEWS CANCER, 2008, 8 (10) :782-798