Norcantharidin induces human melanoma A375-S2 cell apoptosis through mitochondrial and caspase pathways

被引:36
作者
An, W
Wang, M
Tashiro, S
Onodera, S
Ikejima, T [1 ]
机构
[1] Shenyang Pharmaceut Univ, China Japan Res Inst Med & Pharmaceut Sci, Shenyang 110016, Peoples R China
[2] Shenyang Pharmaceut Univ, Dept Pharmacol, Shenyang 110016, Peoples R China
[3] Showa Pharmaceut Univ, Dept Clin & Biomed Sci, Tokyo, Japan
关键词
cantharidin; norcantharidin; cell line; tumor; A375-S2; cells; apoplosis; caspase; mitochondria; proto-oncogene proteins c-bcl-2; cytochromes c;
D O I
10.3346/jkms.2004.19.4.560
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Norcantharidin (NCTD) is the demethylated form of cantharidin, which is the active substance of mylabris. To examine the pathway of NCTD-induced A375-S2 cell death, 3-(4, 5-dimethylthiazol-2-yl)-2, 5-dipheyltetrazolium bromide (MTT) assay, photomicroscopical observation, DNA agarose gel electrophoresis, caspase activity assay and Western blot analysis were carried out. A375-S2 cells treated with NCTD exhibited several typical characteristics of apoptosis. The inhibitory effect of NCTD on human melanoma, A375-S2 cells, was partially reversed by the inhibitors of pan-caspase, caspase-3 and caspase-9. The activities of caspase-3 and -9 were significantly increased after treatment with NCTD at different time. The expression of inhibitor of caspase-activated DNase was decreased in a time-dependent manner, simultaneously, the ratio of Bcl-2/Bax or Bcl-x(L)/Bax was decreased and the expression ratio of proteins could be reversed by caspase-3 inhibitor. The expression of cytochrome c in cytosol was increased after NCTD treatment and caspase-3 inhibitor had no significant effect on the up-regulation of cytochrom c. These results suggest that NCTD induced A375-S2 cell apoptosis and the activation of caspase and mitochondrial pathway were involved in the process of NCTD-induced A375-S2 cell apoptosis.
引用
收藏
页码:560 / 566
页数:7
相关论文
共 31 条
[1]
The Bcl-2 protein family: Arbiters of cell survival [J].
Adams, JM ;
Cory, S .
SCIENCE, 1998, 281 (5381) :1322-1326
[2]
Charrier L, 2002, CANCER RES, V62, P2169
[3]
Bax-independent inhibition of apoptosis by Bcl-x(L) [J].
Cheng, EHY ;
Levine, B ;
Boise, LH ;
Thompson, CB ;
Hardwick, JM .
NATURE, 1996, 379 (6565) :554-556
[4]
Conversion of Bcl-2 to a Bax-like death effector by caspases [J].
Cheng, EHY ;
Kirsch, DG ;
Clem, RJ ;
Ravi, R ;
Kastan, MB ;
Bedi, A ;
Ueno, K ;
Hardwick, JM .
SCIENCE, 1997, 278 (5345) :1966-1968
[5]
Caspase enzyme activity is not essential for apoptosis during thymocyte development [J].
Doerfler, P ;
Forbush, KA ;
Perlmutter, RM .
JOURNAL OF IMMUNOLOGY, 2000, 164 (08) :4071-4079
[6]
A caspase-activated DNase that degrades DNA during apoptosis, and its inhibitor ICAD [J].
Enari, M ;
Sakahira, H ;
Yokoyama, H ;
Okawa, K ;
Iwamatsu, A ;
Nagata, S .
NATURE, 1998, 391 (6662) :43-50
[7]
Gamet-Payrastre L, 2000, CANCER RES, V60, P1426
[8]
Mitochondria and apoptosis [J].
Green, DR ;
Reed, JC .
SCIENCE, 1998, 281 (5381) :1309-1312
[9]
A RAPID AND SIMPLE METHOD FOR THE ISOLATION OF APOPTOTIC DNA FRAGMENTS [J].
HERRMANN, M ;
LORENZ, HM ;
VOLL, R ;
GRUNKE, M ;
WOITH, W ;
KALDEN, JR .
NUCLEIC ACIDS RESEARCH, 1994, 22 (24) :5506-5507
[10]
Multiple extracellular signals promote osteoblast survival and apoptosis [J].
Hill, PA ;
Tumber, A ;
Meikle, MC .
ENDOCRINOLOGY, 1997, 138 (09) :3849-3858