The combination of TRAIL and luteolin enhances apoptosis in human cervical cancer HeLa cells

被引:83
作者
Horinaka, M
Yoshida, T
Shiraishi, T
Nakata, S
Wakada, M
Nakanishi, R
Nishino, H
Sakai, T [1 ]
机构
[1] Kyoto Prefectural Univ Med, Grad Sch Med Sci, Dept Mol Targeting Canc Prevent, Kamigyo Ku, Kyoto 6028566, Japan
[2] Kyoto Prefectural Univ Med, Dept Urol, Kamigyo Ku, Kyoto 6028566, Japan
[3] Kyoto Prefectural Univ Med, Grad Sch Med Sci, Dept Biochem & Mol Biol, Kamigyo Ku, Kyoto 6028566, Japan
关键词
luteolin; DR5; TRAIL; apoptosis; combination; flavonoid; cancer; caspase;
D O I
10.1016/j.bbrc.2005.05.179
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
Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) is one of the most promising candidates for cancer therapeutics. However, some tumor cells are resistant to TRAIL-induced apoptosis. Our previous studies have shown that luteolin, a naturally occurring flavonoid, induces the up-regulation of death receptor 5 (DR5), which is a receptor for TRAIL. Here, we show for the first time that luteolin synergistically acts with exogenous soluble recombinant human TRAIL to induce apoptosis in HeLa cells, but not in normal human peripheral blood mononuclear cells. The combined use of luteolin and TRAIL induced Bid cleavage and the activation of caspase-8. Also, human recombinant DR5/Fc chimera protein, caspase inhibitors, and DR5 siRNA efficiently reduced apoptosis induced by co-treatment with luteolin and TRAIL. These results raise the possibility that this combined treatment with luteolin and TRAIL might be promising as a new therapy against cancer. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:833 / 838
页数:6
相关论文
共 22 条
[1]   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
[2]   CHEMOPREVENTIVE POTENTIAL OF DIETARY BIOFLAVONOIDS AGAINST 20-METHYLCHOLANTHRENE-INDUCED TUMORIGENESIS [J].
ELANGOVAN, V ;
SEKAR, N ;
GOVINDASAMY, S .
CANCER LETTERS, 1994, 87 (01) :107-113
[3]  
GREENBLATT MS, 1994, CANCER RES, V54, P4855
[4]   How melanoma cells evade trail-induced apoptosis [J].
Hersey, P ;
Zhang, XD .
NATURE REVIEWS CANCER, 2001, 1 (02) :142-150
[5]  
HORINAKA M, IN PRESS ONCOGENE
[6]   INHIBITION OF THE MUTAGENICITY OF BAY-REGION DIOL-EPOXIDES OF POLYCYCLIC AROMATIC-HYDROCARBONS BY PHENOLIC PLANT FLAVONOIDS [J].
HUANG, MT ;
WOOD, AW ;
NEWMARK, HL ;
SAYER, JM ;
YAGI, H ;
JERINA, DM ;
CONNEY, AH .
CARCINOGENESIS, 1983, 4 (12) :1631-1637
[7]   Effects of luteolin on the inhibition of proliferation and induction of apoptosis in human myeloid leukaemia cells [J].
Ko, WG ;
Kang, TH ;
Lee, SJ ;
Kim, YC ;
Lee, BH .
PHYTOTHERAPY RESEARCH, 2002, 16 (03) :295-298
[8]   Differential hepatocyte toxicity of recombinant Apo2L/TRAIL versions [J].
Lawrence, D ;
Shahrokh, Z ;
Marsters, S ;
Achilles, K ;
Shih, D ;
Mounho, B ;
Hillan, K ;
Totpal, K ;
DeForge, L ;
Schow, P ;
Hooley, J ;
Sherwood, S ;
Pai, R ;
Leung, S ;
Khan, LL ;
Gliniak, B ;
Bussiere, J ;
Smith, CA ;
Strom, SS ;
Kelley, S ;
Fox, JA ;
Thomas, D ;
Ashkenazi, A .
NATURE MEDICINE, 2001, 7 (04) :383-385
[9]   Identification and molecular cloning of two novel receptors for the cytotoxic ligand TRAIL [J].
MacFarlane, M ;
Ahmad, M ;
Srinivasula, SM ;
FernandesAlnemri, T ;
Cohen, GM ;
Alnemri, ES .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (41) :25417-25420
[10]  
MACGREGOR JT, 1985, PLANT FLAVONOIDS BIO, P411