Anti-estrogenic activity of tris(2,3-dibromopropyl) isocyanurate through disruption of co-activator recruitment: experimental and computational studies
文献类型：期刊论文
| 作者 | Cao, Huiming; Li, Xun; Zhang, Wenjuan; Wang, Ling; Pan, Yu; Zhou, Zhen; Chen, Minjie; Zhang, Aiqian; Liang, Yong; Song, Maoyong
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| 刊名 | ARCHIVES OF TOXICOLOGY
 |
| 出版日期 | 2018-04-01 |
| 卷号 | 92期号:4页码:1471-1482 |
| ISSN号 | 0340-5761 |
| 关键词 | Tris(2,3-dibromopropyl) isocyanurate MVLN assays AF-2 site Molecular dynamics simulations |
| 文献子类 | Article |
| 英文摘要 | As a potential endocrine disruptor, tris(2,3-dibromopropyl) isocyanurate (TBC) has previously been demonstrated to reduce expression of estrogen-dependent vitellogenin (vtg) mRNA in adult zebrafish. However, the underlying toxicity pathways and molecular mechanisms involved in TBC-induced endocrine disruption remain elusive. In the current study, E-Screen and MVLN assays were employed to explore the potential anti-estrogenic effects of TBC via the estrogen receptor alpha (ER alpha)-mediated signaling pathway. Within a dose range between 1 x 10(-9) and 1 x 10(-7) M, TBC significantly inhibited 17 beta-estradiol (E-2)-induced cell proliferation in a breast cancer cell line. The luciferase activity induced by E-2 was also significantly inhibited by TBC in a dose-dependent manner. Moreover, neither TBC nor E-2 affected proliferation of the ER alpha-negative breast cancer cell line MDA-MB-231. These experimental results confirmed that TBC has anti-estrogenic effects by affecting the ER alpha-mediated signaling pathway. By comparing TBC with known antagonists of ER alpha, we found that TBC has similar molecular structure as certain co-activator binding inhibitors. Therefore, using molecular docking and molecular dynamics simulations, TBC was further predicted to competitively occupy the surface site of ER alpha rather than the canonical E-2-binding pocket of ER alpha, thus disrupt subsequent co-activator recruitment and transcription activation. Our findings elucidate the anti-estrogenic mechanism of TBC at the atomic level and highlight the biological importance of surface sites of nuclear receptors for a risk assessment of potential environmental pollutants. |
| 源URL | [http://ir.rcees.ac.cn/handle/311016/40878]  |
| 专题 | 生态环境研究中心_环境化学与生态毒理学国家重点实验室 |
| 推荐引用方式 GB/T 7714 | Cao, Huiming,Li, Xun,Zhang, Wenjuan,et al. Anti-estrogenic activity of tris(2,3-dibromopropyl) isocyanurate through disruption of co-activator recruitment: experimental and computational studies[J]. ARCHIVES OF TOXICOLOGY,2018,92(4):1471-1482. |
| APA | Cao, Huiming.,Li, Xun.,Zhang, Wenjuan.,Wang, Ling.,Pan, Yu.,...&Song, Maoyong.(2018).Anti-estrogenic activity of tris(2,3-dibromopropyl) isocyanurate through disruption of co-activator recruitment: experimental and computational studies.ARCHIVES OF TOXICOLOGY,92(4),1471-1482. |
| MLA | Cao, Huiming,et al."Anti-estrogenic activity of tris(2,3-dibromopropyl) isocyanurate through disruption of co-activator recruitment: experimental and computational studies".ARCHIVES OF TOXICOLOGY 92.4(2018):1471-1482. |
入库方式： OAI收割
来源：生态环境研究中心
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