Emodin induces apoptosis of human cervical cancer cells through poly(ADP-ribose) polymerase cleavage and activation of caspase-9

被引:156
作者
Srinivas, G [1 ]
Anto, RJ [1 ]
Srinivas, P [1 ]
Vidhyalakshmi, S [1 ]
Senan, VP [1 ]
Karunagaran, D [1 ]
机构
[1] Rajiv Gandhi Ctr Biotechnol, Div Canc Biol, Thiruvananthapuram 695014, Kerala, India
关键词
emodin; apoptosis; caspase; cervical cancer; Bu; 25TK;
D O I
10.1016/S0014-2999(03)01976-9
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Emodin (1,3,8-trihydroxy-6-methylanthraquinone) is an active herbal component traditionally used in China for treating various ailments. Emodin exerts antiproliferative effects in many cancer cell lines and the actual molecular mechanism of which is still not clear. Since apoptosis could be a potential mechanism to explain these effects, we tested whether emodin induces cell death in human cervical cancer cells. Our results suggest that emodin exerts antiproliferative effects in human cervical cancer cells. Emodin inhibited DNA synthesis and induced apoptosis as demonstrated by increased nuclear condensation, annexin binding and DNA fragmentation in Bu 25TK cells in the presence of emodin. Moreover, we demonstrate for the first time in human cervical cancer cells that the apoptotic pathway involved in emodin-induced apoptosis is caspase-dependent and presumably through the mitochondrial pathway, as shown by the activation of caspases-3, -9 and cleavage of poly(ADP-ribose) polymerase. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:117 / 125
页数:9
相关论文
共 31 条
[1]   L-929 cells harboring ectopically expressed Re1A resist curcumin-induced apoptosis [J].
Anto, RJ ;
Maliekal, TT ;
Karunagaran, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (21) :15601-15604
[2]   EVALUATION OF THE ANTIVIRAL ACTIVITY OF ANTHRAQUINONES, ANTHRONES AND ANTHRAQUINONE DERIVATIVES AGAINST HUMAN CYTOMEGALOVIRUS [J].
BARNARD, DL ;
HUFFMAN, JH ;
MORRIS, JLB ;
WOOD, SG ;
HUGHES, BG ;
SIDWELL, RW .
ANTIVIRAL RESEARCH, 1992, 17 (01) :63-77
[3]   SELECTIVE-INHIBITION OF THE GROWTH OF RAS-TRANSFORMED HUMAN BRONCHIAL EPITHELIAL-CELLS BY EMODIN, A PROTEIN-TYROSINE KINASE INHIBITOR [J].
CHAN, TCK ;
CHANG, CJ ;
KOONCHANOK, NM ;
GEAHLEN, RL .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 193 (03) :1152-1158
[4]  
Chang CJ, 1996, IN VIVO, V10, P185
[5]   Emodin induces apoptosis in human promyeloleukemic HL-60 cells accompanied by activation of caspase 3 cascade but independent of reactive oxygen species production [J].
Chen, YC ;
Shen, SC ;
Lee, WR ;
Hsu, FL ;
Lin, HY ;
Ko, CH ;
Tseng, SW .
BIOCHEMICAL PHARMACOLOGY, 2002, 64 (12) :1713-1724
[6]   The structures of antioxidant and cytotoxic agents from natural source:: anthraquinones and tannins from roots of Rumex patientia [J].
Demirezer, LÖ ;
Kuruüzüm-Uz, A ;
Bergere, I ;
Schiewe, HJ ;
Zeeck, A .
PHYTOCHEMISTRY, 2001, 58 (08) :1213-1217
[7]  
Du J, 2000, J CELL BIOCHEM, V77, P333, DOI 10.1002/(SICI)1097-4644(20000501)77:2<333::AID-JCB15>3.0.CO
[8]  
2-Q
[9]   IMMUNOSUPPRESSIVE EFFECT OF EMODIN, A FREE-RADICAL GENERATOR [J].
HUANG, HC ;
CHANG, JH ;
TUNG, SF ;
WU, RT ;
FOEGH, ML ;
CHU, SH .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1992, 211 (03) :359-364
[10]   Possible involvement of cytochrome c release and sequential activation of caspases in ceramide-induced apoptosis in SK-N-MC cells [J].
Ito, A ;
Uehara, T ;
Tokumitsu, A ;
Okuma, Y ;
Nomura, Y .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 1999, 1452 (03) :263-274