Prolonged re-expression of the hypermethylated gene EPB41L3 using artificial transcription factors and epigenetic drugs

Epigenetics. 2015;10(5):384-96. doi: 10.1080/15592294.2015.1034415. Epub 2015 Apr 1.

Abstract

Epigenetic silencing of tumor suppressor genes (TSGs) is considered a significant event in the progression of cancer. For example, EPB41L3, a potential biomarker in cervical cancer, is often silenced by cancer-specific promoter methylation. Artificial transcription factors (ATFs) are unique tools to re-express such silenced TSGs to functional levels; however, the induced effects are considered transient. Here, we aimed to improve the efficiency and sustainability of gene re-expression using engineered zinc fingers fused to VP64 (ZF-ATFs) or DNA methylation modifiers (ZF-Tet2 or ZF-TDG) and/or by co-treatment with epigenetic drugs [5-aza-2'-deoxycytidine or Trichostatin A (TSA)]. The EPB41L3-ZF effectively bound its methylated endogenous locus, as also confirmed by ChIP-seq. ZF-ATFs reactivated the epigenetically silenced target gene EPB41L3 (∼ 10-fold) in breast, ovarian, and cervical cancer cell lines. Prolonged high levels of EPB41L3 (∼ 150-fold) induction could be achieved by short-term co-treatment with epigenetic drugs. Interestingly, for otherwise ineffective ZF-Tet2 or ZF-TDG treatments, TSA facilitated re-expression of EPB41L3 up to twofold. ATF-mediated re-expression demonstrated a tumor suppressive role for EPB41L3 in cervical cancer cell lines. In conclusion, epigenetic reprogramming provides a novel way to improve sustainability of re-expression of epigenetically silenced promoters.

Keywords: DNA demethylases; anti-cancer drug response; artificial transcription factors; epigenome editing; methylation biomarkers; novel antitumor agents.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / pharmacology*
  • Azacitidine / analogs & derivatives
  • Azacitidine / pharmacology
  • Cell Line, Tumor
  • DNA Methylation / drug effects*
  • Decitabine
  • Epigenesis, Genetic*
  • Gene Expression Regulation, Neoplastic / drug effects*
  • Histone Code / drug effects
  • Histone Deacetylases / metabolism
  • Humans
  • Hydroxamic Acids / pharmacology
  • Microfilament Proteins / metabolism*
  • RNA, Messenger / metabolism
  • Transcription Factors / chemistry
  • Transcription Factors / metabolism*

Substances

  • Antineoplastic Agents
  • EPB41L3 protein, human
  • Hydroxamic Acids
  • Microfilament Proteins
  • RNA, Messenger
  • Transcription Factors
  • trichostatin A
  • Decitabine
  • Histone Deacetylases
  • Azacitidine