Cytotoxicity of perillyl alcohol against cancer cells is potentiated by hyperthermia

被引:12
作者
Ahn, KJ
Lee, CK
Choi, EK
Griffin, R
Song, CW
Park, HJ
机构
[1] Univ Minnesota, Sch Med, Dept Therapeut Radiol, Radiobiol Lab, Minneapolis, MN 55455 USA
[2] Univ Ulsan, Coll Med, Dept Therapeut Radiol, Seoul, South Korea
[3] Inha Univ, Coll Med, Dept Microbiol, Inchon, South Korea
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2003年 / 57卷 / 03期
关键词
perillyl alcohol; hyperthermia; apoptosis; SCK tumor cells;
D O I
10.1016/S0360-3016(03)00737-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Perillyl alcohol (POH) (4-isopropenyl-cyclohexenecarbinol) is a member of the monoterpenes, which are present in various fruits and vegetables. POH has been demonstrated to be cytotoxic against a variety of experimental cancer cells in vitro and in vivo. Phase I clinical trials have indicated that POH may be useful for human tumor treatment. The purpose of our study was to reveal whether the anticancer effect of POH could be enhanced by hyperthermia. Methods and Materials: SCK mammary carcinoma cells of A/J mice were used. The effects of POH or hyperthermia alone were studied by incubating the cells during exponential growth phase in culture with 0.25-1.0 mM of POH at 37degreesC for varying lengths of time or heating cells at 41-43degreesC for varying lengths of time. The combined effect of POH and hyperthermia was investigated by heating the cells with 1 mM of POH at 41-43degreesC for varying lengths of time. The effects of the treatments were evaluated using the clonogenic cell survival assay and three types of apoptosis assays. Results: An incubation of SCK cells with 1 mM of POH at 37degreesC for 60 min or hyperthermia at 43degreesC for 1 h decreased clonogenic cell survival to 40% and 60%, respectively. When the cells were heated at 43degreesC for 1 h in the presence of 1 mM of POH, clonogenic cell survival decreased to 0.2%, indicating that hyperthermia potentiated the effect of POH to cause clonogenic cell death. Hyperthermia also markedly increased the degree of POH-induced apoptosis. Conclusion: Hyperthermia synergistically potentiates the cytotoxicity of naturally occurring POH against cancer cells. (C) 2003 Elsevier Inc.
引用
收藏
页码:813 / 819
页数:7
相关论文
共 52 条
[1]  
Ariazi EA, 1999, CANCER RES, V59, P1917
[2]   A TRANSFORMING GROWTH-FACTOR-BETA TYPE-I RECEPTOR THAT SIGNALS TO ACTIVATE GENE-EXPRESSION [J].
BASSING, CH ;
YINGLING, JM ;
HOWE, DJ ;
WANG, TW ;
HE, WW ;
GUSTAFSON, ML ;
SHAH, P ;
DONAHOE, PK ;
WANG, XF .
SCIENCE, 1994, 263 (5143) :87-89
[3]  
Belanger J T, 1998, Altern Med Rev, V3, P448
[4]   Cytotoxicity and biotransformation of the anticancer drug perillyl alcohol in PC12 cells and in the rat [J].
Boon, PJM ;
van der Boon, D ;
Mulder, GJ .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2000, 167 (01) :55-62
[5]   Antileukemia activity of perillyl alcohol (POH): uncoupling apoptosis from G0/G1 arrest suggests that the primary effect of POH on Bcr/Abl-transformed cells is to induce growth arrest [J].
Clark, SS ;
Perman, SM ;
Sahin, MB ;
Jenkins, GJ ;
Elegbede, JA .
LEUKEMIA, 2002, 16 (02) :213-222
[6]   Prevention and therapy of cancer by dietary monoterpenes [J].
Crowell, PL .
JOURNAL OF NUTRITION, 1999, 129 (03) :775S-778S
[7]  
CROWELL PL, 1994, CRIT REV ONCOGENESIS, V5, P1
[8]  
CROWELL PL, 1991, J BIOL CHEM, V266, P17679
[9]   STRUCTURE-ACTIVITY-RELATIONSHIPS AMONG MONOTERPENE, INHIBITORS OF PROTEIN ISOPRENYLATION AND CELL-PROLIFERATION [J].
CROWELL, PL ;
REN, ZB ;
LIN, SZ ;
VEDEJS, E ;
GOULD, MN .
BIOCHEMICAL PHARMACOLOGY, 1994, 47 (08) :1405-1415
[10]   Referee: Hyperthermia alone or combined with cisplatin in addition to radiotherapy for advanced uterine cervical cancer [J].
Dahl, O ;
Mella, O .
INTERNATIONAL JOURNAL OF HYPERTHERMIA, 2002, 18 (01) :25-30