Epigenetic modulation of BRCA1 and BRCA2 gene expression by equol in breast cancer cell lines

被引:37
作者
Bosviel, Remy [1 ,2 ]
Durif, Julie [1 ,2 ]
Dechelotte, Pierre [2 ,3 ]
Bignon, Yves-Jean [1 ,2 ]
Bernard-Gallon, Dominique [1 ,2 ]
机构
[1] Ctr Jean Perrin, Dept Oncogenet, CBRV, F-63001 Clermont Ferrand, France
[2] Univ Auvergne, EA 4233, F-63001 Clermont Ferrand, France
[3] CHU, Nouvel Hop Estaing, Serv Anat Pathol, F-63100 Clermont Ferrand, France
关键词
Equol; Breast cancer susceptibility genes 1 and 2; Breast cancer; TUMOR-SUPPRESSOR GENES; PROMOTER HYPERMETHYLATION; DNA METHYLATION; SOY PHYTOESTROGENS; CYCLE ARREST; GENISTEIN; ISOFLAVONES; BINDING; DEMETHYLATION; DAIDZEIN;
D O I
10.1017/S000711451100657X
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
S-Equol is a metabolite resulting from the conversion of daidzein, a soya phyto-oestrogen, by the gut microflora. The potential protective effects of equol in breast cancer are still under debate. Consequently, we investigated the effects of equol on DNA methylation of breast cancer susceptibility genes (BRCA1 and BRCA2) and oncosuppressors in breast cancer cell lines (MDA-MB-231 and MCF-7) and in a dystrophic breast cell line (MCF-10a) following exposure to S-equol (2 mu M) for 3 weeks. We demonstrated by quantitative analysis of methylated alleles a significant decrease in the methylation of the cytosine phosphate guanine (CpG) islands in the promoters of BRCA1 and BRCA2 after the S-equol treatment in MCF-7 and MDA-MB-231 cells and a trend in MCF-10a cells. We also showed that S-equol increases BRCA1 and BRCA2 protein expression in the nuclei and the cytoplasm in MCF-7, MDA-MB-231 and MCF-10a cell lines by immunohistochemistry. The increase in BRCA1 and BRCA2 proteins was also found after Western blotting in the studied cell lines. In summary, we demonstrated the demethylating effect of S-equol on the CpG islands inside the promoters of BRCA1 and BRCA2 genes, resulting in an increase in the level of expressed oncosuppressors in breast cancer cell lines.
引用
收藏
页码:1187 / 1193
页数:7
相关论文
共 59 条
[1]   THE IDENTIFICATION OF THE WEAK ESTROGEN EQUOL [7-HYDROXY-3-(4'-HYDROXYPHENYL)CHROMAN] IN HUMAN-URINE [J].
AXELSON, M ;
KIRK, DN ;
FARRANT, RD ;
COOLEY, G ;
LAWSON, AM ;
SETCHELL, KDR .
BIOCHEMICAL JOURNAL, 1982, 201 (02) :353-357
[2]   ELISA as a new method to measure genistein and daidzein in food and human fluids [J].
Bennetau-Pelissero, C ;
Arnal-Schnebelen, B ;
Lamothe, V ;
Sauvant, P ;
Sagne, JL ;
Verbruggen, MA ;
Mathey, J ;
Lavialle, O .
FOOD CHEMISTRY, 2003, 82 (04) :645-658
[3]   Epigenetic Control of Estrogen Receptor Expression and Tumor Suppressor Genes Is Modulated by Bioactive Food Compounds [J].
Berner, Carolin ;
Aumueller, Eva ;
Gnauck, Anne ;
Nestelberger, Manuela ;
Just, A. ;
Haslberger, Alexander G. .
ANNALS OF NUTRITION AND METABOLISM, 2011, 57 (3-4) :183-189
[4]   Functions of the BRGA1 and BRCA2 genes [J].
Bertwistle, D ;
Ashworth, A .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1998, 8 (01) :14-20
[5]   Peripheral blood DNA methylation detected in the BRCA1 or BRCA2 promoter for sporadic ovarian cancer patients and controls [J].
Bosviel, Remy ;
Michard, Emilie ;
Lavediaux, Guillaume ;
Kwiatkowski, Fabrice ;
Bignon, Yves-Jean ;
Bernard-Gallon, Dominique J. .
CLINICA CHIMICA ACTA, 2011, 412 (15-16) :1472-1475
[6]   Novel consensus DNA-binding sequence for BRCA1 protein complexes [J].
Cable, PL ;
Wilson, CA ;
Calzone, FJ ;
Rauscher, FJ ;
Scully, R ;
Livingston, DM ;
Li, LP ;
Blackwell, CB ;
Futreal, PA ;
Afshari, CA .
MOLECULAR CARCINOGENESIS, 2003, 38 (02) :85-96
[7]   BREAST TUMOR-CELL LINES FROM PLEURAL EFFUSIONS [J].
CAILLEAU, R ;
YOUNG, R ;
OLIVE, M ;
REEVES, WJ .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1974, 53 (03) :661-674
[8]  
Choi EJ, 2008, MOL MED REP, V1, P239
[9]   Methylation status of CpG islands at sites-59 to+96 in exon 1 of the BRCA2 gene varies in mammary tissue among women with sporadic breast cancer [J].
Cucer, Nurhan ;
Taheri, Serpil ;
Ok, Engin ;
Ozkul, Yusuf .
JOURNAL OF GENETICS, 2008, 87 (02) :155-158
[10]   DNA methylation and cancer [J].
Das, PM ;
Singal, R .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (22) :4632-4642