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

• Published in: The Journal of steroid biochemistry and molecular biology Vol. 141; pp. 160 - 170
• Main Authors: Bhan, Arunoday, Hussain, Imran, Ansari, Khairul I., Bobzean, Samara A.M., Perrotti, Linda I., Mandal, Subhrangsu S.
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01.05.2014
• Subjects: Acetylation; Animals; Base Sequence; Benzhydryl Compounds - toxicity; Bisphenol A; Breast Neoplasms - genetics; Breast Neoplasms - metabolism; Diethylstilbestrol; Diethylstilbestrol - toxicity; Endocrine disruption; Endocrine Disruptors - toxicity; Epigenetics; Estradiol - pharmacology; Female; Gene Expression - drug effects; Gene Expression Regulation, Neoplastic - drug effects; Histone-Lysine N-Methyltransferase; Histones - metabolism; HOTAIR; Humans; LncRNA; Mammary Glands, Animal - drug effects; Mammary Glands, Animal - metabolism; MCF-7 Cells; Myeloid-Lymphoid Leukemia Protein - metabolism; Phenols - toxicity; Protein Binding; Protein Processing, Post-Translational; Rats; Rats, Sprague-Dawley; Receptors, Estrogen - metabolism; Response Elements; RNA, Long Noncoding - genetics; RNA, Long Noncoding - metabolism; Transcriptional Activation - drug effects; Transcriptional regulation; HOTAIR; Bisphenol A; Endocrine disruption; LncRNA; Epigenetics; Diethylstilbestrol; Transcriptional regulation
• ISSN: 0960-0760; 1879-1220
• DOI: 10.1016/j.jsbmb.2014.02.002

•Long non-coding RNA HOTAIR is a key player in breast cancer.•HOTAIR is induced by endocrine disruptors BPA and DES in vitro and in vivo.•MLL-histone methylases and ERs coordinate the BPA/DES-induced HOTAIR expression.•BPA/DES alter the histone methylation/acetylation status at the HOTAIR promoter.•Revealed novel epigenetic mechanism of endocrine disruption of lncRNA HOTAIR. 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.