Chemopreventive properties of the ethanol extract of chinese licorice (Glycyrrhiza uralensis) root:: induction of apoptosis and G1 cell cycle arrest in MCF-7 human breast cancer cells

被引:118
作者
Jo, EH
Kim, SH
Ra, JC
Kim, SR
Cho, SD
Jung, JW
Yanga, SR
Park, JS
Hwang, JW
Aruoma, OI
Kim, TY
Lee, YS
Kang, KS
机构
[1] Seoul Natl Univ, Coll Vet Med, Dept Vet Publ Hlth, Seoul 151742, South Korea
[2] Kyung Hee Univ, Grad Sch EW Med Sci, Seoul, South Korea
[3] RNL Life Sci Ltd, Suwon, Kyunggi, South Korea
[4] Korea Food Res Inst, Sungnam, South Korea
[5] S Bank Univ, Dept Appl Sci, London SE1 0AA, England
[6] Minist Agr & Forestry, Div Anim Hlth, Kwacheon, South Korea
关键词
breast cancer; Chinese licorice root; Glycyrrhiza uralensis; apoptosis; chemoprevention; cell cycle arrest;
D O I
10.1016/j.canlet.2004.12.038
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Much of the interest on the chemopreventive properties of licorice has been focused on the plant genius Glycyrrhiza glabra. In this study the ethanol extract of Chinese licorice root, Glycyrrhiza uralensis (G. uralensis) was investigated for its estrogenic effect and the ability to inhibit cell proliferation in the MCF-7 human breast cancer cell line. The extract of the root of G. uralensis was fractionated in EtOH:H2O (80:20) (80% ethanol). The extract exhibited estrogenic effects similar to 17 beta-estradiol (E2) and induced apoptosis at the same dose level (100 mu g/ml) in MCF-7 breast cancer cells, results were associated with up-regulation of tumor suppressor gene p53 and pro-apoptotic protein Bax. G. uralensis extract caused the up-regulation of p21(waf1/cip1) and downregulation of cdk 2 and cyclin E and most significantly, induced G1 cell cycle arrest. This is the first study to show that the ethanolic extract of the root of G. uralensis has an estrogen-like activity and anti-cancer effects against MCF-7 human breast cancer cells. Whilst the use of phytoestrogens to protect against hormone-dependent cancers or as a 'natural' alternative to hormone replacement therapy remains controversial, the data in this paper support the suggestion that extracts of root of the Chinese licorice G. uralensis might be of importance in this debate. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:239 / 247
页数:9
相关论文
共 29 条
[1]
Phyto-oestrogens and cancer [J].
Adlercreutz, H .
LANCET ONCOLOGY, 2002, 3 (06) :364-373
[2]
Human ICE/CED-3 protease nomenclature [J].
Alnemri, ES ;
Livingston, DJ ;
Nicholson, DW ;
Salvesen, G ;
Thornberry, NA ;
Wong, WW ;
Yuan, JY .
CELL, 1996, 87 (02) :171-171
[3]
EXPRESSION OF THE BCL-2 GENE FAMILY IN NORMAL AND MALIGNANT BREAST-TISSUE - LOW BAX-ALPHA EXPRESSION IN TUMOR-CELLS CORRELATES WITH RESISTANCE TOWARDS APOPTOSIS [J].
BARGOU, RC ;
DANIEL, PT ;
MAPARA, MY ;
BOMMERT, K ;
WAGENER, C ;
KALLINICH, B ;
ROYER, HD ;
DORKEN, B .
INTERNATIONAL JOURNAL OF CANCER, 1995, 60 (06) :854-859
[4]
Estrogen and antiestrogen regulation of cell cycle progression in breast cancer cells [J].
Doisneau-Sixou, SF ;
Sergio, CM ;
Carroll, JS ;
Hui, R ;
Musgrove, EA ;
Sutherland, RL .
ENDOCRINE-RELATED CANCER, 2003, 10 (02) :179-186
[5]
Estrogen regulates activity of cyclin-dependent kinases and retinoblastoma protein phosphorylation in breast cancer cells [J].
Foster, JS ;
Wimalasena, J .
MOLECULAR ENDOCRINOLOGY, 1996, 10 (05) :488-498
[6]
Hayashi H, 2003, BIOL PHARM BULL, V26, P867, DOI 10.1248/bpb.26.867
[7]
Phytoestrogen consumption and breast cancer risk in a multiethnic population - The Bay Area Breast Cancer Study [J].
Horn-Ross, PL ;
John, EM ;
Lee, M ;
Stewart, SL ;
Koo, J ;
Sakoda, LC ;
Shiau, AG ;
Goldstein, J ;
Davis, P ;
Perez-Stable, EJ .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 2001, 154 (05) :434-441
[8]
Ganoderma lucidum extract induces cell cycle arrest and apoptosis in MCF-7 human breast cancer cell [J].
Hu, HB ;
Ahn, NS ;
Yang, XL ;
Lee, YS ;
Kang, KS .
INTERNATIONAL JOURNAL OF CANCER, 2002, 102 (03) :250-253
[9]
Breast cancer: hormones and other risk factors [J].
Hulka, BS ;
Moorman, PG .
MATURITAS, 2001, 38 (01) :103-113
[10]
Molecular epidemiology and carcinogenesis: endogenous and exogenous carcinogens [J].
Hussain, SP ;
Harris, CC .
MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH, 2000, 462 (2-3) :311-322