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
[1]   2-Methoxyestradiol inhibits superoxide anion generation while it enhances superoxide dismutase activity in swine granulosa cells [J].
Basini, Giuseppina ;
Santini, Sujen Eleonora ;
Grasselli, Francesca .
SIGNAL TRANSDUCTION PATHWAYS, PT B: STRESS SIGNALING AND TRANSCRIPTIONAL CONTROL, 2006, 1091 :34-40
[2]   Antioxidants, oxidative damage and oxygen deprivation stress: a review [J].
Blokhina, O ;
Virolainen, E ;
Fagerstedt, KV .
ANNALS OF BOTANY, 2003, 91 (02) :179-194
[3]   The permeability transition pore complex in cancer cell death [J].
Brenner, C. ;
Grimm, S. .
ONCOGENE, 2006, 25 (34) :4744-4756
[4]  
CARTER WO, 1994, J LEUKOCYTE BIOL, V55, P253
[5]   Reactive oxygen species production is involved in quercetin-induced apoptosis in human hepatoma cells [J].
Chang, Yuh-Fang ;
Chi, Chin-Wen ;
Wang, Jane-Jen .
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL, 2006, 55 (02) :201-209
[6]   2-methoxyestradiol induces apoptosis in Ewing sarcoma cells through mitochondrial hydrogen peroxide production [J].
Djavaheri-Mergny, M ;
Wietzerbin, J ;
Besançon, F .
ONCOGENE, 2003, 22 (17) :2558-2567
[7]  
FOTSIS T, 1994, NATURE, V368, P237, DOI 10.1038/368237a0
[8]   2-methoxyestradiol-induced apoptosis in human leukemia cells proceeds through a reactive oxygen species and Akt-dependent process [J].
Gao, N ;
Rahmani, M ;
Dent, P ;
Grant, S .
ONCOGENE, 2005, 24 (23) :3797-3809
[9]   Antitumor effects of photodynamic therapy are potentiated by 2-methoxyestradiol -: A superoxide dismutase inhibitor [J].
Golab, J ;
Nowis, D ;
Skrzycki, M ;
Czeczot, H ;
Baranczyk-Kuzma, A ;
Wilczynski, GM ;
Makowski, M ;
Mróz, P ;
Kozar, K ;
Kaminski, R ;
Jalili, A ;
Kopec, M ;
Grzela, T ;
Jakóbisiak, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (01) :407-414
[10]  
Heerdt BG, 1998, CANCER RES, V58, P2869