Green tea polyphenols as potent enhancers of glucocorticoid-induced mouse mammary tumor virus gene expression

被引:15
作者
Abe, I [1 ]
Umehara, K [1 ]
Morita, R [1 ]
Nemoto, K [1 ]
Degawa, M [1 ]
Noguchi, H [1 ]
机构
[1] Univ Shizuoka, Sch Pharmaceut Sci, Shizuoka 4228526, Japan
关键词
glucocorticoid; reporter gene assay; mouse mammary tumor virus promoter; human immunodeficiency virus; green tea polyphenols; (-)-epigallocatechin-3-O-gallate; n-dodecyl gallate; gallic acid; galloylesters; regulation of gene expression;
D O I
10.1006/bbrc.2001.4325
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The effect of natural and synthetic galloyl esters on glucocorticoid-induced gene expression was evaluated by using rat fibroblast 3Y1 cells stably transfected with a luciferase reporter gene under the transcriptional regulation of the mouse mammary tumor virus promoter. The glucocorticoid-induced gene transcription was strongly suppressed by synthetic alkyl esters; n-dodecyl gallate showed the most potent inhibition (66% inhibition at 10 muM), which was far more potent than that of crude tannic acid, n-Octyl and n-cetyl gallate also showed good inhibition, while gallic acid itself was not so active, suggesting that the presence of hydrophobic side chain is important for the suppressive effect. On the other hand, surprisingly, green tea gallocatechins, (-)-epigallocatechin-3-O-gallate and theasinensin A, potently enhanced the promoter activity (182 and 247% activity at 1 muM, respectively). The regulation of the level of the glucocorticoid-induced gene expression by the antioxidative gallates is of great interest from a therapeutic point of view. (C) 2001 Academic Press.
引用
收藏
页码:122 / 125
页数:4
相关论文
共 17 条
[1]   Potent and selective inhibition of squalene epoxidase by synthetic galloyl esters [J].
Abe, I ;
Seki, T ;
Noguchi, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 270 (01) :137-140
[2]   Green tea polyphenols: Novel and potent inhibitors of squalene epoxidase [J].
Abe, I ;
Seki, T ;
Umehara, K ;
Miyase, T ;
Noguchi, H ;
Sakakibara, J ;
Ono, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 268 (03) :767-771
[3]   STEROID-HORMONE RECEPTOR STATUS DEFINES THE MMTV PROMOTER CHROMATIN STRUCTURE IN-VIVO [J].
ARCHER, TK ;
FRYER, CJ ;
LEE, HL ;
ZANIEWSKI, E ;
LIANG, T ;
MYMRYK, JS .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1995, 53 (1-6) :421-429
[4]   Angiogenesis inhibited by drinking tea [J].
Cao, YH ;
Cao, RH .
NATURE, 1999, 398 (6726) :381-381
[5]   Mechanisms of anti-inflammatory action and of immunosuppression by glucocorticoids: negative interference of activated glucocorticoid receptor with transcription factors [J].
De Bosscher, K ;
Vanden Berghe, W ;
Haegeman, G .
JOURNAL OF NEUROIMMUNOLOGY, 2000, 109 (01) :16-22
[6]   Why drinking green tea could prevent cancer [J].
Jankun, J ;
Selman, SH ;
Swiercz, R ;
SkrzypczakJankun, E .
NATURE, 1997, 387 (6633) :561-561
[7]   INHIBITION OF HUMAN SPLEEN PROTEIN-TYROSINE KINASES BY PHENOLIC-COMPOUNDS [J].
LAZARO, I ;
PALACIOS, C ;
GONZALES, M ;
GONZALEZPORQUE, P .
ANALYTICAL BIOCHEMISTRY, 1995, 225 (01) :180-183
[8]  
Nakagawa K, 1997, J NUTR SCI VITAMINOL, V43, P679, DOI 10.3177/jnsv.43.679
[9]  
Saeki K, 2000, BIOL PHARM BULL, V23, P1391, DOI 10.1248/bpb.23.1391
[10]   Derivatives of gallic acid induce apoptosis in tumoral cell lines and inhibit lymphocyte proliferation [J].
Serrano, A ;
Palacios, C ;
Roy, G ;
Cespón, C ;
Villar, ML ;
Nocito, M ;
González-Porqué, P .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1998, 350 (01) :49-54