Asiatic acid induces apoptosis in SK-MEL-2 human melanoma cells

被引:127
作者
Park, BC
Bosire, KO
Lee, ES
Lee, YS
Kim, JA [1 ]
机构
[1] Yeungnam Univ, Coll Pharm, Kyongsan 712749, South Korea
[2] Duksung Womens Univ, Coll Pharm, Seoul 132714, South Korea
关键词
asiatic acid; apoptosis; melanoma; reactive oxygen species; Bax; caspase-3;
D O I
10.1016/j.canlet.2004.06.039
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Asiatic acid (AA) is a pentacyclic triterpene found in Centella asiatica. In the present study, the mechanism of anticancer effect of AA on skin cancer was investigated. AA decreased viability and induced apoptosis in human melanoma SK-MEL-2 cells in a time- and dose-dependent manner. AA also markedly increased intracellular reactive oxygen species (ROS) level and enhanced the expression of Bax but not Bcl-2 protein in the cells. In addition, AA-induced activation of caspase-3 activity in a dose-dependent manner. Pretreatment with Trolox, an antioxidant, significantly blocked the induction of Bax and activation of caspase-3 in AA-treated cells. Furthermore, Ac-DEVD-CHO, a specific caspase-3 inhibitor, and Trolox prevented the AA-induced apoptosis. AA did not elevate p53 nuclear protein levels that are present in a mutant form in SK-MEL-2 cells. These results suggest that AA-induced apoptosis may be mediated through generation of ROS, alteration of Bax/Bcl-2 ratio and activation of caspase-3, but p53-independent. These results further suggest that AA may be a good candidate for the therapeutic intervention of human skin cancer. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:81 / 90
页数:10
相关论文
共 42 条
[11]   Bcl-2 is an apoptotic target suppressed by both c-Myc and E2F-1 [J].
Eischen, CM ;
Packham, G ;
Nip, J ;
Fee, BE ;
Hiebert, SW ;
Zambetti, GP ;
Cleveland, JL .
ONCOGENE, 2001, 20 (48) :6983-6993
[12]   Dual regulation of caspase activity by hydrogen peroxide: Implications for apoptosis [J].
Hampton, MB ;
Orrenius, S .
FEBS LETTERS, 1997, 414 (03) :552-556
[13]   BCL-2 IS AN INNER MITOCHONDRIAL-MEMBRANE PROTEIN THAT BLOCKS PROGRAMMED CELL-DEATH [J].
HOCKENBERY, D ;
NUNEZ, G ;
MILLIMAN, C ;
SCHREIBER, RD ;
KORSMEYER, SJ .
NATURE, 1990, 348 (6299) :334-336
[14]  
HUANG MT, 1994, CANCER RES, V54, P701
[15]   PROGRAMMED CELL-DEATH AND BCL-2 PROTECTION IN VERY-LOW OXYGEN [J].
JACOBSON, MD ;
RAFF, MC .
NATURE, 1995, 374 (6525) :814-816
[16]   Structure-activity relationship study of asiatic acid derivatives against beta amyloid (Aβ)-induced neurotoxicity [J].
Jew, SS ;
Yoo, CH ;
Lim, DY ;
Kim, H ;
Mook-Jung, I ;
Jung, MW ;
Choi, H ;
Jung, YH ;
Kim, H ;
Park, HG .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2000, 10 (02) :119-121
[17]   P53, CELL-CYCLE CONTROL AND APOPTOSIS - IMPLICATIONS FOR CANCER [J].
KASTAN, MB ;
CANMAN, CE ;
LEONARD, CJ .
CANCER AND METASTASIS REVIEWS, 1995, 14 (01) :3-15
[18]   Proteolytic activities that mediate apoptosis [J].
Kidd, VJ .
ANNUAL REVIEW OF PHYSIOLOGY, 1998, 60 :533-573
[19]   Current status of the molecular mechanisms of anticancer drug-induced apoptosis - The contribution of molecular-level analysis to cancer chemotherapy [J].
Kim, R ;
Tanabe, K ;
Uchida, Y ;
Emi, M ;
Inoue, H ;
Toge, T .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2002, 50 (05) :343-352
[20]   A novel p53 mutant retained functional activity in lung carcinomas [J].
Ko, JL ;
Chiao, MC ;
Chang, SL ;
Lin, PP ;
Lin, JC ;
Sheu, GT ;
Lee, H .
DNA REPAIR, 2002, 1 (09) :755-762