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

J Steroid Biochem Mol Biol. 2014 May:141:160-70. doi: 10.1016/j.jsbmb.2014.02.002. Epub 2014 Feb 14.

Abstract

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.

Keywords: Bisphenol A; Diethylstilbestrol; Endocrine disruption; Epigenetics; HOTAIR; LncRNA; Transcriptional regulation.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylation
  • Animals
  • Base Sequence
  • Benzhydryl Compounds / toxicity*
  • Breast Neoplasms / genetics
  • Breast Neoplasms / metabolism*
  • Diethylstilbestrol / toxicity*
  • Endocrine Disruptors / toxicity*
  • Estradiol / pharmacology
  • Female
  • Gene Expression / drug effects
  • Gene Expression Regulation, Neoplastic / drug effects
  • Histone-Lysine N-Methyltransferase
  • Histones / metabolism
  • Humans
  • MCF-7 Cells
  • Mammary Glands, Animal / drug effects
  • Mammary Glands, Animal / metabolism
  • Myeloid-Lymphoid Leukemia Protein / metabolism
  • Phenols / toxicity*
  • Protein Binding
  • Protein Processing, Post-Translational
  • RNA, Long Noncoding / genetics*
  • RNA, Long Noncoding / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Estrogen / metabolism
  • Response Elements
  • Transcriptional Activation / drug effects*

Substances

  • Benzhydryl Compounds
  • Endocrine Disruptors
  • HOTAIR long untranslated RNA, human
  • Histones
  • KMT2A protein, human
  • Phenols
  • RNA, Long Noncoding
  • Receptors, Estrogen
  • Myeloid-Lymphoid Leukemia Protein
  • Estradiol
  • Diethylstilbestrol
  • Histone-Lysine N-Methyltransferase
  • bisphenol A