Research and Development Division, Nihon Nohyaku Co. Ltd., 345 Oyamada-cho, Kawachi-nagano, Osaka, Japan.
Reprod Toxicol. 2013 Jan;35:1-6. doi: 10.1016/j.reprotox.2012.11.001. Epub 2012 Nov 10.
Androgen receptor (AR) is an essential component to activate AR dependent gene transcriptions. Despite wide acceptance of pharmacological controls on transcriptional pathway depending on competitive inhibitions of ligand binding, only a few examples, AR antagonism via ligand-independent mechanisms, have been recognized. Pyrifluquinazon(PFQ), a newly developed pesticide, induced representative AR antagonism against rats in in vivo and in vitro. Intriguingly, this AR antagonism was not based on inhibition of ligand binding. Instead, the evidence suggested that the AR antagonism was induced as a consequence of decline of cellular AR protein level. This study demonstrated that AR N-terminal region could be an essential element for a ligand-independent mechanism underling the AR antagonism by PFQ. Our findings should provide a novel insight into the regulation of AR-mediated transcription.
雄激素受体 (AR) 是激活 AR 依赖基因转录所必需的组成部分。尽管人们广泛接受通过竞争性抑制配体结合来控制转录途径的药理学方法,但仅识别出少数几种通过非配体依赖机制的 AR 拮抗作用的例子。吡氟氯禾灵 (PFQ) 是一种新开发的农药,在体内和体外均能诱导大鼠产生代表性的 AR 拮抗作用。有趣的是,这种 AR 拮抗作用不是基于配体结合的抑制。相反,有证据表明,AR 拮抗作用是由于细胞内 AR 蛋白水平下降而引起的。本研究表明,AR N 端区域可能是 PFQ 诱导的 AR 拮抗作用的非配体依赖机制的一个重要因素。我们的研究结果应该为 AR 介导的转录调控提供新的见解。