Tartrazine and sunset yellow are xenoestrogens in a new screening assay to identify modulators of human oestrogen receptor transcriptional activity

被引:68
作者
Axon, Andrew [1 ,3 ]
May, Felicity E. B. [2 ]
Gaughan, Luke E. [2 ]
Williams, Faith M. [3 ]
Blain, Peter G. [3 ]
Wright, Matthew C. [1 ,3 ]
机构
[1] Newcastle Univ, Sch Med, Inst Cellular Med, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
[2] Newcastle Univ, No Canc Res Inst, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
[3] Newcastle Univ, Med Toxicol Ctr, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
关键词
Food additive; Cosmetic additive; Oestrogen receptors; Primary biliary cirrhosis; Cholestasis; MCF-7; cells; PRIMARY BILIARY-CIRRHOSIS; GENE-EXPRESSION; RISK-FACTORS; IN-VITRO; CELLS; PHYTOESTROGENS; INHIBITION; ESTRADIOL; INSIGHTS; TIP60;
D O I
10.1016/j.tox.2012.04.014
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Primary biliary cirrhosis (PBC) is a cholestatic liver disease of unknown cause that occurs most frequently in post-menopausal women. Since the female sex hormone oestrogen can be cholestatic, we hypothesised that PBC may be triggered in part by chronic exposure to xenoestrogens (which may be more active on a background of low endogenous oestrogen levels seen in post-menopausal women). A reporter gene construct employing a synthetic oestrogen response element predicted to specifically interact with oestrogen receptors (ER) was constructed. Co-transfection of this reporter into an ER null cell line with a variety of nuclear receptor expression constructs indicated that the reporter gene was trans-activated by ER alpha and ER beta, but not by the androgen, thyroid, progesterone, glucocorticoid or vitamin D receptors. Chemicals linked to PBC were then screened for xenoestrogen activity in the human ER alpha-positive MCF-7 breast cancer cell line. Using this assay, the coal-derived food and cosmetic colourings - sunset yellow and tartrazine - were identified as novel human ERa activators, activating the human ER with an EC50% concentration of 220 and 160 nM, respectively. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:40 / 51
页数:12
相关论文
共 44 条
[31]
Are Transient Environmental Agents Involved in the Cause of Primary Biliary Cirrhosis? Evidence from Space-Time Clustering Analysis [J].
McNally, Richard J. Q. ;
Ducker, Samantha ;
James, Oliver F. W. .
HEPATOLOGY, 2009, 50 (04) :1169-1174
[32]
Regulation of postnatal lung development and homeostasis by estrogen receptor β [J].
Patrone, C ;
Cassel, TN ;
Pettersson, K ;
Piao, YS ;
Cheng, GJ ;
Ciana, P ;
Maggi, A ;
Warner, M ;
Gustafsson, JÅ ;
Nord, M .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (23) :8542-8552
[33]
Case-control studies of risk factors for primary biliary cirrhosis in two United Kingdom populations [J].
Prince, M. I. ;
Ducker, S. J. ;
James, O. F. W. .
GUT, 2010, 59 (04) :508-512
[34]
Endotoxemia and Gut Barrier Dysfunction in Alcoholic Liver Disease [J].
Rao, Radhakrishna .
HEPATOLOGY, 2009, 50 (02) :638-644
[35]
Some alkyl hydroxy benzoate preservatives (parabens) are estrogenic [J].
Routledge, EJ ;
Parker, J ;
Odum, J ;
Ashby, J ;
Sumpter, JP .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1998, 153 (01) :12-19
[36]
Drug- and estrogen-induced cholestasis through inhibition of the hepatocellular bile salt export pump (Bsep) of rat liver [J].
Stieger, B ;
Fattinger, K ;
Madon, J ;
Kullak-Ublick, GA ;
Meier, PJ .
GASTROENTEROLOGY, 2000, 118 (02) :422-430
[37]
Gut-Liver Axis and Sensing Microbes [J].
Szabo, Gyongyi ;
Bala, Shashi ;
Petrasek, Jan ;
Gattu, Arijeet .
DIGESTIVE DISEASES, 2010, 28 (06) :737-744
[38]
MOLECULAR MECHANISMS OF ACTION OF STEROID/THYROID RECEPTOR SUPERFAMILY MEMBERS [J].
TSAI, MJ ;
OMALLEY, BW .
ANNUAL REVIEW OF BIOCHEMISTRY, 1994, 63 :451-486
[39]
WAKELING AE, 1991, CANCER RES, V51, P3867
[40]
Xenobiotic Incorporation into Pyruvate Dehydrogenase Complex Can Occur Via the Exogenous Lipoylation Pathway [J].
Walden, Hannah R. ;
Kirby, John A. ;
Yeaman, Stephen J. ;
Gray, Joe ;
Jones, David E. ;
Palmer, Jeremy M. .
HEPATOLOGY, 2008, 48 (06) :1874-1884