Red clover and soy isoflavones-an in vitro safety assessment

被引:17
作者
Reiter, Evelyne [1 ,2 ]
Gerster, Petra [1 ,2 ]
Jungbauer, Alois [1 ,2 ]
机构
[1] Univ Nat Resources & Life Sci Vienna, Dept Biotechnol, A-1190 Vienna, Austria
[2] Christian Doppler Lab Receptor Biotechnol, Vienna, Austria
关键词
apoptosis; cell cycle arrest; cell proliferation; isoflavones; red clover; soy; BREAST-CANCER CELLS; UP-REGULATION; ATHYMIC MICE; MCF-7; TUMORS; BIOCHANIN-A; NUDE-MICE; GENISTEIN; GROWTH; ESTROGEN; APOPTOSIS;
D O I
10.3109/09513590.2011.588743
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Isoflavones from red clover and soy plant extracts are used in highly concentrated food supplements as an alternative to hormone replacement therapy. Due to their estrogenic activity, isoflavones are a focus of safety concerns about their potential to promote the growth of hormone-dependent cancer cells. In this study, isoflavones and plant extracts were tested for their effect on cell proliferation, apoptosis induction and cell cycle arrest. Isoflavones and plant extracts were applied in proliferation assays on 11 human cancer cell lines (representing cancers of the colon, prostate, breast, cervix, liver, pancreas, stomach and ovaries) and a fibroblast line to detect cytotoxic activity. Fluorescence-activated cell sorting was used to detect the induction of apoptosis or cell cycle arrest. Isoflavones and plant extracts significantly reduced the proliferation activity of the treated cancer cell lines. Growth promotion was not observed, but apoptosis or necrosis induction was, as was cell cycle arrest, with genistein as the most potent isoflavone. Isoflavones and plant extracts from soy and red clover, respectively, do not promote the growth of human cancer cells but induce decreased cell proliferation, increased apoptosis and cell cycle arrest. These results indicate that isoflavones can be considered safe compounds.
引用
收藏
页码:1037 / 1042
页数:6
相关论文
共 30 条
[1]  
Allred CD, 2001, CANCER RES, V61, P5045
[2]   The Combination of TRAIL and Isoflavones Enhances Apoptosis in Cancer Cells [J].
Bronikowska, Joanna ;
Szliszka, Ewelina ;
Czuba, Zenon P. ;
Zwolinski, Dariusz ;
Szmydki, Dariusz ;
Krol, Wojciech .
MOLECULES, 2010, 15 (03) :2000-2015
[3]   Genistein affests hepatoma cells at G2/M phase:: involvement of ATM activation and upregulation of p21waf1/cip1 and Wee1 [J].
Chang, KL ;
Kung, ML ;
Chow, NH ;
Su, SJ .
BIOCHEMICAL PHARMACOLOGY, 2004, 67 (04) :717-726
[4]   Genistein induces maturation of cultured human breast cancer cells and prevents tumor growth in nude mice [J].
Constantinou, AI ;
Krygier, AE ;
Mehta, RR .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1998, 68 (06) :1426S-1430S
[5]   Low Concentrations of the Soy Phytoestrogen Genistein Induce Proteinase Inhibitor 9 and Block Killing of Breast Cancer Cells by Immune Cells [J].
Jiang, Xinguo ;
Patterson, Nicole M. ;
Ling, Yan ;
Xie, Jianwei ;
Helferich, William G. ;
Shapiro, David J. .
ENDOCRINOLOGY, 2008, 149 (11) :5366-5373
[6]   Effects of dietary daidzein and its metabolite, equol, at physiological concentrations on the growth of estrogen-dependent human breast cancer (MCF-7) tumors implanted in ovariectomized athymic mice [J].
Ju, YH ;
Fultz, J ;
Allred, KF ;
Doerge, DR ;
Helferich, WG .
CARCINOGENESIS, 2006, 27 (04) :856-863
[7]  
Ju YH, 2002, CANCER RES, V62, P2474
[8]   Dietary genistein negates the inhibitory effect of letrozole on the growth of aromatase-expressing estrogen-dependent human breast cancer cells (MCF-7Ca) in vivo [J].
Ju, Young H. ;
Doerge, Daniel R. ;
Woodling, Kellie A. ;
Hartman, James A. ;
Kwak, Jieun ;
Helferich, William G. .
CARCINOGENESIS, 2008, 29 (11) :2162-2168
[9]   Induction of apoptosis in breast cancer cells MDA-MB-231 by genistein [J].
Li, YW ;
Upadhyay, S ;
Bhuiyan, M ;
Sarkar, FH .
ONCOGENE, 1999, 18 (20) :3166-3172
[10]   Genistein-induced G2-M arrest, p21WAF1 upregulation, and apoptosis in a non-small-cell lung cancer cell line [J].
Lian, FR ;
Bhuiyan, M ;
Li, YW ;
Wall, N ;
Kraut, M ;
Sarkar, FH .
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL, 1998, 31 (03) :184-191