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

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.

主权项

1. A method of identifying a candidate compound which may inhibit overexpression of α9-nAChR in nicotine-derived-compound-induced breast cancer cells in an advanced stage, comprising contacting the compound with the AP1 polypeptide or VDR polypeptide and determining whether the compound binds to the polypeptide, wherein binding of the compound to the polypeptide indicates that the compound may inhibit overexpression of α9-nAChR in nicotine-derived-compound-induced breast cancer cells in an advanced stage; wherein the AP1 polypeptide is encoded by a polynucleotide comprising a sequence of nnTGAC(or G)nnnnn (SEQ ID NO:1 or SEQ ID NO:2), and wherein the VDR polypeptide is encoded by a polynucleotide comprising a sequence of nnnnnnnnGAGG(or T)nnn (SEQ ID NO:3 or SEQ ID NO:4).