报告基因
化学
邻苯二甲酸盐
雌激素受体
邻苯二甲酸二丁酯
兴奋剂
受体
内分泌干扰物
体外
雌激素受体α
生物
生物化学
基因表达
基因
内分泌系统
激素
遗传学
癌症
有机化学
乳腺癌
作者
Chengyu Lv,Zhengyi Wei,Benjie Yue,Ning Xia,Wei Huang,Yulan Yue,Zhuolin Li,Tiezhu Li,Xiuxia Zhang,Yongjun Wang
标识
DOI:10.1080/15376516.2021.1998276
摘要
Phthalate esters (PAEs) are important pollutants in the environment, which can interfere with the endocrine system by mimicking estrogen. However, limited information is available on modulating the estrogen receptor (ER) of five PAEs including di (2-ethylhexyl) phthalate (DEHP), diisononyl phthalate (DINP), benzyl butyl phthalate (BBP), diphenyl phthalate (DPhP) and dicyclohexyl phthalate (DCHP). This study evaluated the agonistic effects of PAEs on human ER. The cytotoxicity assay showed that there were a significant inhibition of the cell proliferation with treatment of five PAEs. Moreover, DPhP does-dependently enhanced ER-mediated transcriptional activity in the reporter gene assay. The increased expression of estrogen-responsive genes (TFF1, CTSD, and GREB1) was also observed in MCF-7 cells treated with DPhP. The result of molecular docking showed that DPhP tended to bind to the agonist conformation of ER compared with the antagonist conformation of ER, demonstrating its agonist characteristic that has been confirmed in the reporter gene assay. Thus, we found that DPhP may be evaluated as an ER agonist in vitro and it can interfere with the normal function of human ER.
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