Reversal of hypermethylation and reactivation of p16INK4a RARβ, and MGMT genes by genistein and other isoflavones from soy

被引:296
作者
Fang, MZ
Chen, DP
Sun, Y
Jin, Z
Christman, JK
Yang, CS
机构
[1] Rutgers State Univ, Dept Biol Chem, Ernest Mario Sch Pharm, Susan Lehman Cullman Lab Canc Res, Piscataway, NJ 08854 USA
[2] Univ Nebraska Med Ctr, Dept Biochem & Mol Biol, Omaha, NE USA
[3] Univ Nebraska Med Ctr, UNMC Eppley Canc Ctr, Omaha, NE USA
关键词
D O I
10.1158/1078-0432.CCR-05-0406
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: We have previously shown the reactivation of some methylation-silenced genes in cancer cells by (-)-epigallocatechin-3-gallate, the major polyphenol from green tea. To determine whether other polyphenolic compounds have similar activities, we studied the effects of soy isoflavones on DNA methylation. Experimental Design: Enzyme assay was used to determine the inhibitory effect of genistein on DNA methyltransferase activity in nuclear extracts and purified recombinant enzyme. Methylation-specific PCR and quantitative real-time PCR were employed to examine the DNA methylation and gene expression status of retinoic acid receptor beta (RAR beta), p16(INK4a), and O-6-methylguanine,methyltransferase (MGMT) in KYSE 510 esophageal squamous cell carcinoma cells treated with genistein alone or in combination with trichostatin, sulforaphane, or 2'-deoxy-5- aza-cyticline (5-aza-dCyd). Results: Genistein (2-20 mu mol/L) reversed DNA hypermethylation and reactivated RAR beta, p16(INK4a), and MGMT in KYSE 510 cells. Genistein also inhibited cell growth at these concentrations. Reversal of DNA hypermethylation and reactivation of RAR beta by genistein were also observed in KYSE 150 cells and prostate cancer LNCaP and PC3 cells. Genistein (20-50 mu mol/L) dose-dependently inhibited DNA methyltransferase activity, showing substrate- and methyl donor-dependent inhibition. Biochanin A and daidzein Were less effective in inhibiting DNA methy transferase activity, in reactivating RAR beta, and in inhibiting cancer cell growth. In combination with trichostatin, sulforaphane, or 5-aza-dCyd, genistein enhanced reactivation of these genes and inhibition of cell growth. Conclusions:These results indicate that genistein and related soy isoflavones reactivate methylation-silenced genes, partially through a direct inhibition of DNA methyltransferase, which may contribute to the chemopreventive activity of dietary isoflavones.
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页码:7033 / 7041
页数:9
相关论文
共 55 条
[1]   MICROASSAY FOR DNA METHYLTRANSFERASE [J].
ADAMS, RLP ;
RINALDI, A ;
SEIVWRIGHT, C .
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS, 1991, 22 (01) :19-22
[2]  
ADLERCREUTZ CHT, 1995, J NUTR, V125, pS757, DOI 10.1093/jn/125.3_Suppl.757S
[3]  
AKIYAMA T, 1987, J BIOL CHEM, V262, P5592
[4]   Estrogen receptor β mRNA in colon cancer cells:: Growth effects of estrogen and genistein [J].
Arai, N ;
Ström, A ;
Rafter, JJ ;
Gustafsson, JÅ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 270 (02) :425-431
[5]   Real-time quantitative PCR as a routine method for screening large rearrangements in Rett syndrome: Report of one case of MECP2 deletion and one case of MECP2 duplication [J].
Ariani, F ;
Mari, F ;
Pescucci, C ;
Longo, I ;
Bruttini, M ;
Meloni, I ;
Hayek, G ;
Rocchi, R ;
Zappella, M ;
Renieri, A .
HUMAN MUTATION, 2004, 24 (02) :172-177
[6]  
Badia E, 2000, CANCER RES, V60, P4130
[7]   Increased cytosine DNA-methyltransferase activity is target-cell-specific and an early event in lung cancer [J].
Belinsky, SA ;
Nikula, KJ ;
Baylin, SB ;
Issa, JPJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (09) :4045-4050
[8]   Optimization of baculovirus-mediated expression and purification of hexahistidine-tagged murine DNA (cytosine-C5)-methyltransferase-1 in Spodoptera frugiperda 9 cells [J].
Brank, AS ;
Van Bemmel, DM ;
Christman, JK .
PROTEIN EXPRESSION AND PURIFICATION, 2002, 25 (01) :31-40
[9]   Prepubertal estradiol and genistein exposures up-regulate BRCA1 mRNA and reduce mammary tumorigenesis [J].
Cabanes, A ;
Wang, M ;
Olivo, S ;
DeAssis, S ;
Gustafsson, JÅ ;
Khan, G ;
Hilakivi-Clarke, L .
CARCINOGENESIS, 2004, 25 (05) :741-748
[10]   5-Azacytidine and 5-aza-2′-deoxycytidine as inhibitors of DNA methylation:: mechanistic studies and their implications for cancer therapy [J].
Christman, JK .
ONCOGENE, 2002, 21 (35) :5483-5495