Epigenetic reactivation of p21CIP1/WAF1 and KLOTHO by a combination of bioactive dietary supplements is partially ERα-dependent in ERα-negative human breast cancer cells

Mol Cell Endocrinol. 2015 May 5:406:102-14. doi: 10.1016/j.mce.2015.02.020. Epub 2015 Feb 25.

Abstract

Available treatment strategies against estrogen receptor (ER)-negative breast cancer patients are limited due to their poor response to hormonal therapy. We have shown previously that the combinations of green tea polyphenols (GTPs), a dietary DNA methyltransferase inhibitor, and sulforaphane (SFN), a dietary histone deacetylase inhibitor, reactivate ERα expression in ERα-negative MDA-MB-231 cells. Here, we investigated the functional significance of ERα reactivation in the reactivation of silenced tumor suppressor genes (TSGs) in ERα-negative human breast cancer cells. We found that the treatment of MDA-MB-231 cells with the combinations of GTPs and SFN leads to the reactivation of silenced TSGs such as p21(CIP1/WAF1) and KLOTHO through active chromatin modifications. Further, GTPs- and SFN-mediated reactivation of TSGs was, at least in part, dependent on ERα reactivation in ERα-negative MDA-MB-231 cells. Collectively, our findings suggest that a novel combination of bioactive dietary supplements could further be explored as an effective therapeutic option against hormonal refractory breast cancer.

Keywords: Breast cancer; Epigenetics; Estrogen receptor; Green tea; Sulforaphane; Tumor suppressor genes.

Publication types

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

MeSH terms

  • Breast Neoplasms / genetics*
  • Cell Cycle Checkpoints / drug effects
  • Cell Line, Tumor
  • Chromatin / metabolism
  • Cyclin-Dependent Kinase Inhibitor p21 / genetics*
  • DNA Methylation / drug effects
  • DNA Methylation / genetics
  • Dietary Supplements*
  • Epigenesis, Genetic* / drug effects
  • Estrogen Receptor alpha / genetics*
  • Estrogen Receptor alpha / metabolism*
  • Female
  • Glucuronidase / genetics*
  • Histones / metabolism
  • Humans
  • Insulin-Like Growth Factor I / metabolism
  • Isothiocyanates / pharmacology
  • Klotho Proteins
  • Polyphenols / pharmacology
  • Promoter Regions, Genetic / genetics
  • Protein Processing, Post-Translational / drug effects
  • Signal Transduction / drug effects
  • Sulfoxides
  • Tea / chemistry

Substances

  • Chromatin
  • Cyclin-Dependent Kinase Inhibitor p21
  • ESR1 protein, human
  • Estrogen Receptor alpha
  • Histones
  • Isothiocyanates
  • Polyphenols
  • Sulfoxides
  • Tea
  • Insulin-Like Growth Factor I
  • Glucuronidase
  • Klotho Proteins
  • sulforaphane