The role of early life genistein exposures in modifying breast cancer risk

被引:107
作者
Warri, A. [3 ]
Saarinen, N. M. [3 ]
Makela, S. [4 ]
Hilakivi-Clarke, L. [1 ,2 ]
机构
[1] Georgetown Univ, Washington, DC 20057 USA
[2] Vincent T Lombardi Canc Res Ctr, Dept Oncol, Washington, DC 20057 USA
[3] Univ Turku, Turku, Finland
[4] Univ Turku, Dept Biochem & Food Chem, Turku, Finland
关键词
breast cancer; tumour suppressors; epigenetic; mammary stem cell; genistein; soy;
D O I
10.1038/sj.bjc.6604321
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Review of the existing literature suggests that consumption of soy foods or an exposure to a soy isoflavone genistein during childhood and adolescence in women, and before puberty onset in animals, reduces later mammary cancer risk. In animal studies, an exposure that is limited to the fetal period or adult life does not appear to have the same protective effect. A meta-analysis of human studies indicates a modest reduction in pre- and postmenopausal risk when dietary intakes are assessed during adult life. These findings concur with emerging evidence indicating that timing may be vitally important in determining the effects of various dietary exposures on the susceptibility to develop breast cancer. In this review, we address the mechanisms that might mediate the effects of an early life exposure to genistein on the mammary gland. The focus is on changes in gene expression, such as those involving BRCA1 and PTEN. It will be debated whether mammary stem cells are the targets of genistein-induced alterations and also whether the alterations are epigenetic. We propose that the effects on mammary gland morphology and signalling pathways induced by pubertal exposure to genistein mimic those induced by the oestrogenic environment of early first pregnancy.
引用
收藏
页码:1485 / 1493
页数:9
相关论文
共 58 条
[41]   PTENless means more [J].
Stiles, B ;
Groszer, M ;
Wang, SY ;
Jiao, J ;
Wu, H .
DEVELOPMENTAL BIOLOGY, 2004, 273 (02) :175-184
[42]   Exposure to soy-based formula in infancy and endocrinological and reproductive outcomes in young adulthood [J].
Strom, BL ;
Schinnar, R ;
Ziegler, EE ;
Barnhart, KT ;
Sammel, MD ;
Macones, GA ;
Stallings, VA ;
Drulis, JM ;
Nelson, SE ;
Hanson, SA .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 286 (07) :807-814
[43]   Expression profiling of rat mammary epithelial cells reveals candidate signaling pathways in dietary protection from mammary tumors [J].
Su, Ying ;
Simmen, Frank A. ;
Xiao, Rijin ;
Simmen, Rosalia C. M. .
PHYSIOLOGICAL GENOMICS, 2007, 30 (01) :8-16
[44]   In utero exposure to maternal diets containing soy protein isolate, but not genistein alone, protects young adult rat offspring from NMU-induced mammary tumorigenesis [J].
Su, Ying ;
Eason, Renea R. ;
Geng, Yan ;
Till, S. R. ;
Badger, Thomas M. ;
Simmen, Rosalia C. M. .
CARCINOGENESIS, 2007, 28 (05) :1046-1051
[45]  
TANY WY, 2007, REV ENDOCR METAB DIS, V8, P173
[46]   Estrogenic effect of soy isoflavones on mammary gland morphogenesis and gene expression profile [J].
Thomsen, Anni R. ;
Almstrup, Kristian ;
Nielsen, John E. ;
Sorensen, Ilona K. ;
Petersen, Ole William ;
Leffers, Henrik ;
Breinholt, Vibeke M. .
TOXICOLOGICAL SCIENCES, 2006, 93 (02) :357-368
[47]  
Thomsen AR, 2005, NUTR CANCER, V52, P176, DOI 10.1207/s15327914nc5202_8
[48]   Genistein inhibits Brca1 mutant tumor growth through activation of DNA damage checkpoints, cell cycle arrest, and mitotic catastrophe [J].
Tominaga, Y. ;
Wang, A. ;
Wang, R-H ;
Wang, X. ;
Cao, L. ;
Deng, C-X .
CELL DEATH AND DIFFERENTIATION, 2007, 14 (03) :472-479
[49]   Towards an integrated model for breast cancer etiology - The crucial role of the number of mammary tissue-specific stem cells [J].
Trichopoulos, D ;
Lagiou, P ;
Adami, HO .
BREAST CANCER RESEARCH, 2005, 7 (01) :13-17
[50]   Meta-analysis of soy intake and breast cancer risk [J].
Trock, BJ ;
Hilakivi-Clarke, L ;
Clarke, R .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2006, 98 (07) :459-471