具有对雌激素受体α和β的强效和亚型选择性作用的黄类药物的表征
Michael J Bolt1,2, Jessica Oceguera1,2, Pankaj K Singh1,2
1Center for Advanced Microscopy and Image Informatics, Institute of Biosciences & Technology, Texas A&M University, and Baylor College of Medicine, Houston, TX 77030, USA.
iScience
|March 12, 2024
概括
这项研究选了224种对雌激素受体 (ERα和ERβ) 的活性,确定了激活这些受体的众多化合物. 这些发现突出了饮食中的黄类药物中潜在的内分泌干扰剂.
科学领域:
- 内分泌学 在内分泌学.
- 分子生物学分子生物学
- 毒理学 毒理学 毒理学
背景情况:
- 雌激素受体 (ERα和ERβ) 通过结合来调节基因转录.
- 饮食和环境中的植物化学物质可以与激素通路相互作用,可能破坏生理功能.
- 了解黄类药物与雌激素信号的相互作用,对于评估它们对人类健康的影响至关重要.
研究的目的:
- 选大量的黄类药物库,以检测它们对雌激素受体 (ERα和ERβ) 的活性.
- 为了描述黄类-ER相互作用的亚型选择性和强度.
- 使用体内模型验证已识别的黄类的雌激素潜力.
主要方法:
- 使用工程ERα和ERβPRL阵列细胞系对224种黄类的选.
- 在雌激素信号通路的多个步骤中对黄类活性的表征.
- 使用转基因斑马鱼体内活体模型验证雌激素活性.
主要成果:
- 确定了83种激活ERα和96种激活ERβ的黄类.
- 观察到双重作用和亚型选择性黄类,其中一些具有强烈的亚微分子活性.
- 在斑马鱼模型中验证了选定的化合物的雌激素潜力.
结论:
- 这项研究代表了迄今为止在ER途径上对黄素的最大查.
- 确定了大量具有ERα和/或ERβ激活特性的黄类药物.
- 这些发现有助于识别影响雌激素信号传递的新型潜在内分泌干扰物.
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