Quercetin Induces Oxidative Stress and Potentiates the Apoptotic Action of 2-Methoxyestradiol in Human Hepatoma Cells

被引:54
作者
Chang, Yuh-Fang [1 ]
Hsu, Yi-Chiung [2 ]
Hung, Hui-Fang [1 ]
Lee, Hui-Ju [2 ]
Lui, Wing-Yiu [1 ]
Chi, Chin-Wen [1 ,2 ]
Wang, Jane-Jen [3 ]
机构
[1] Taipei Vet Gen Hosp, Taipei 112, Taiwan
[2] Natl Yang Ming Univ, Taipei 112, Taiwan
[3] Natl Taipei Coll Nursing, Taipei 112, Taiwan
来源
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL | 2009年 / 61卷 / 05期
关键词
HUMAN LEUKEMIA-CELLS; SUPEROXIDE-DISMUTASE; HYDROGEN-PEROXIDE; HEPATOCELLULAR-CARCINOMA; CANCER-CELLS; GROWTH; ACTIVATION; GENERATION; PATHWAYS; PROLIFERATION;
D O I
10.1080/01635580902825571
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hepatocellular carcinoma (HCC) is the leading cause of cancer mortality in Asia. This study evaluated the growth inhibition effect of quercetin and 2-methoxyestradiol in vitro in human HCC cell lines. Combination treatment enhanced the cytotoxic effect in HA22T/VGH and HepG2 cell lines as compared with quercetin or 2-methoxyestradiol alone. The cell population of sub-G0/G1 phase and the level of annexin V binding were increased synergistically after combination treatment with quercetin and 2-methoxyestradiol in both cell lines. Moreover, quercetin combined with 2-methoxyestradiol increased superoxide levels, mitochondrial superoxide dismutase (MnSOD) in mRNA, protein levels, and SOD activity. Finally, we also found the mitochondrial membrane potential was decreased after combination treatment. The changes of reactive oxygen species and mitochondrial disruption were likely to be involved in the mechanism for the synergistic cytotoxicity effects of combination treatment in human hepatoma cells. These results provided a basis for further study of the potential usage of quercetin combination with hormonal agents for the treatment of human hepatoma.
引用
收藏
页码:735 / 745
页数:11
相关论文
共 42 条
[21]  
2-7
[22]  
Lin HL, 2001, CANCER, V92, P500, DOI 10.1002/1097-0142(20010801)92:3<500::AID-CNCR1348>3.0.CO
[23]  
2-4
[24]   Male predominance in hepatocellular carcinoma: new insight and a possible therapeutic alternative [J].
Lui, WY ;
Lin, HL ;
Chau, GY ;
Liu, TY ;
Chi, CW .
MEDICAL HYPOTHESES, 2000, 55 (04) :348-350
[25]   Quercetin may act as a cytotoxic prooxidant after its metabolic activation to semiquinone and quinoidal product [J].
Metodiewa, D ;
Jaiswal, AK ;
Cenas, N ;
Dickancaité, E ;
Segura-Aguilar, J .
FREE RADICAL BIOLOGY AND MEDICINE, 1999, 26 (1-2) :107-116
[26]   Food-derived polyphenols inhibit pancreatic cancer growth through mitochondrial cytochrome c release and apoptosis [J].
Mouria, M ;
Gukovskaya, AS ;
Jung, Y ;
Buechler, P ;
Hines, OJ ;
Reber, HA ;
Pandol, SJ .
INTERNATIONAL JOURNAL OF CANCER, 2002, 98 (05) :761-769
[27]   Reactive oxygen species in mitochondria-mediated cell death [J].
Orrenius, Sten .
DRUG METABOLISM REVIEWS, 2007, 39 (2-3) :443-455
[28]   Mitochondrial superoxide dismutase: A promising target for new anticancer therapies [J].
Pani, G ;
Colavitti, R ;
Bedogni, B ;
Fusco, S ;
Ferraro, D ;
Borrello, S ;
Galeotti, T .
CURRENT MEDICINAL CHEMISTRY, 2004, 11 (10) :1299-1308
[29]   Inhibition of mitochondrial respiration - A novel strategy to enhance drug-induced apoptosis in human leukemia cells by a reactive oxygen species-mediated mechanism [J].
Pelicano, H ;
Feng, L ;
Zhou, Y ;
Carew, JS ;
Hileman, EO ;
Plunkett, W ;
Keating, MJ ;
Huang, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (39) :37832-37839
[30]   Imbalance of antioxidant enzymes in tumor cells and inhibition of proliferation and malignant features by scavenging hydrogen peroxide [J].
Policastro, L ;
Molinari, B ;
Larcher, F ;
Blanco, P ;
Podhajcer, OL ;
Costa, CS ;
Rojas, P ;
Dur n, H .
MOLECULAR CARCINOGENESIS, 2004, 39 (02) :103-113