Bisphenol-A and diethylstilbestrol exposure induces the expression of breast cancer associated long noncoding RNA HOTAIR in vitro and in vivo

被引:128
作者
Bhan, Arunoday [1 ]
Hussain, Imran [1 ]
Ansari, Khairul I. [1 ]
Bobzean, Samara A. M. [2 ]
Perrotti, Linda I. [2 ]
Mandal, Subhrangsu S. [1 ]
机构
[1] Univ Texas Arlington, Dept Chem & Biochem, Arlington, TX 76019 USA
[2] Univ Texas Arlington, Dept Psychol, Arlington, TX 76019 USA
基金
美国国家卫生研究院;
关键词
Endocrine disruption; HOTAIR; LncRNA; Bisphenol A; Diethylstilbestrol; Transcriptional regulation; Epigenetics; NUCLEAR RECEPTOR SUPERFAMILY; MAMMARY-GLAND DEVELOPMENT; MLL HISTONE METHYLASES; ESTROGEN-RECEPTOR; ENDOCRINE DISRUPTORS; GENE-EXPRESSION; UTERO EXPOSURE; CRITICAL ROLES; TUMOR-GROWTH; CHROMATIN;
D O I
10.1016/j.jsbmb.2014.02.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Antisense transcript, long non-coding RNA HOTAIR is a key player in gene silencing and breast cancer and is transcriptionally regulated by estradiol. Here, we have investigated if HOTAIR expression is misregulated by bisphenol-A (BPA) and diethylstilbestrol (DES). Our findings demonstrate BPA and DES induce HOTAIR expression in cultured human breast cancer cells (MCF7) as well as in vivo in the mammary glands of rat. Luciferase assay showed that HOTAIR promoter estrogen-response-elements (EREs) are induced by BPA and DES. Estrogen-receptors (ERs) and ER-coregulators such as MLL-histone methylases (MLL1 and MLL3) bind to the HOTAIR promoter EREs in the presence of BPA and DES, modify chromatin (histone methylation and acetylation) and lead to gene activation. Knockdown of ERs down-regulated the BPA and DES-induced expression of HOTAIR. In summary, our results demonstrate that BPA and DES exposure alters the epigenetic programming of the HOTAIR promoters leading to its endocrine disruption in vitro and in vivo. Published by Elsevier Ltd.
引用
收藏
页码:160 / 170
页数:11
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