首页> 外国专利> Method of identifying a candidate compound which may inhibit α9-nAchR overexpression or estrogen receptor-dependent transcription in nicotine-derived-compound-induced breast cancer cells

Method of identifying a candidate compound which may inhibit α9-nAchR overexpression or estrogen receptor-dependent transcription in nicotine-derived-compound-induced breast cancer cells

机译:鉴定可能抑制尼古丁衍生化合物诱导的乳腺癌细胞中α9-nAchR过表达或雌激素受体依赖性转录的候选化合物的方法

摘要

The invention relates to methods of identifying a candidate compound which may inhibit estrogen receptor-dependent transcription or α9-nAChR overexpression and proliferation of nicotine-derived-compound-induced breast cancer cells by using an activating protein 1 (AP1) polypeptide. The invention found that α9-nAChR has an activating protein 1 (AP1)-binding site, that the α9-nAChR promoter is located at the AP1-binding site, and that ERs specifically bind to the α9-nAChR promoter at the AP1-binding site, indicating that ER-induced α9-nAChR up-regulation plays a central role in the response to endogenous (E2) or exogenous (nicotine) stimulation.
机译:本发明涉及通过使用活化蛋白1(AP1)多肽来鉴定可抑制雌激素受体依赖性转录或α9-nAChR过表达和烟碱衍生化合物诱导的乳腺癌细胞增殖的候选化合物的方法。本发明发现α9-nAChR具有活化蛋白1(AP1)结合位点,α9-nAChR启动子位于AP1结合位点,并且ER在AP1结合处特异性地与α9-nAChR启动子结合。该位点表明,ER诱导的α9-nAChR上调在对内源性(E2)或外源性(尼古丁)刺激的反应中起关键作用。

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