首页> 外文期刊>Toxicology: An International Journal Concerned with the Effects of Chemicals on Living Systems >Tartrazine and sunset yellow are xenoestrogens in a new screening assay to identify modulators of human oestrogen receptor transcriptional activity
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Tartrazine and sunset yellow are xenoestrogens in a new screening assay to identify modulators of human oestrogen receptor transcriptional activity

机译:tartrazine和日落黄是一种新的筛选测定法中的异雌激素,用于鉴定人类雌激素受体转录活性的调节剂

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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 ERα and ERβ, 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 ERα-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 ERα activators, activating the human ER with an EC 50% concentration of 220 and 160nM, respectively.
机译:原发性胆汁性肝硬化(PBC)是一种原因不明的胆汁淤积性肝病,在绝经后妇女中最常见。由于女性性激素的雌激素可能是胆汁淤积的,因此我们假设PBC可能部分由长期暴露于异雌激素(在绝经后妇女体内内源性雌激素水平较低的背景下更为活跃)触发。构建了报道基因基因构建体,该报告体基因构建体采用了预期与雌激素受体(ER)特异性相互作用的合成雌激素反应元件。将该报告基因与多种核受体表达构建体共转染到ER空细胞系中,表明该报告基因被ERα和ERβ反式激活,但未被雄激素,甲状腺,孕酮,糖皮质激素或维生素D受体反式激活。然后针对人ERα阳性MCF-7乳腺癌细胞系筛选与PBC相关的化学物质的异雌激素活性。使用该测定法,将煤衍生的食品和化妆品着色剂(日落黄和酒石黄)鉴定为新型人ERα激活剂,分别以50%EC浓度220和160nM激活人ER。

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