Disruption of BRD4 at H3K27Ac-enriched enhancer region correlates with decreased c-Myc expression in Merkel cell carcinoma

Epigenetics. 2015;10(6):460-6. doi: 10.1080/15592294.2015.1034416. Epub 2015 May 5.

Abstract

Pathologic c-Myc expression is frequently detected in human cancers, including Merkel cell carcinoma (MCC), an aggressive skin cancer with no cure for metastatic disease. Bromodomain protein 4 (BRD4) regulates gene transcription by binding to acetylated histone H3 lysine 27 (H3K27Ac) on the chromatin. Super-enhancers of transcription are identified by enrichment of H3K27Ac. BET inhibitor JQ1 disrupts BRD4 association with super-enhancers, downregulates proto-oncogenes, such as c-Myc, and displays antitumor activity in preclinical animal models of human cancers. Here we show that an enhancer proximal to the c-Myc promoter is enriched in H3K27Ac and associated with high occupancy of BRD4, and coincides with a putative c-Myc super-enhancer in MCC cells. This observation is mirrored in tumors from MCC patients. Importantly, depleted BRD4 occupancy at the putative c-Myc super-enhancer region by JQ1 correlates with decreased c-Myc expression. Thus, our study provides initial evidence that super-enhancers regulate c-Myc expression in MCC.

Keywords: BET inhibitor; BET, bromodomain and extra-terminal domain family; BRD, bromodomain; BRD4; ChIP, Chromatin immunoprecipitation; H3K27Ac; JQ1; MCC, Merkel cell carcinoma; Merkel cell carcinoma; qPCR, quantitative PCR; qRT-PCR, quantitative reverse transcription PCR; super-enhancer.

Publication types

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

MeSH terms

  • Acetylation / drug effects
  • Animals
  • Apoptosis / drug effects
  • Azepines / administration & dosage
  • Carcinoma, Merkel Cell / drug therapy
  • Carcinoma, Merkel Cell / genetics*
  • Carcinoma, Merkel Cell / metabolism
  • Cell Cycle Proteins
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Chromatin
  • Enhancer Elements, Genetic / genetics
  • Epigenesis, Genetic / genetics*
  • Gene Expression Regulation, Neoplastic / drug effects
  • Humans
  • Jumonji Domain-Containing Histone Demethylases / genetics
  • Mice
  • Neoplasm Metastasis
  • Nuclear Proteins / genetics*
  • Nuclear Proteins / metabolism
  • Promoter Regions, Genetic
  • Protein Binding
  • Proto-Oncogene Proteins c-myb / biosynthesis*
  • Proto-Oncogene Proteins c-myb / genetics
  • Skin Neoplasms / drug therapy
  • Skin Neoplasms / genetics*
  • Skin Neoplasms / metabolism
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism
  • Triazoles / administration & dosage
  • Xenograft Model Antitumor Assays

Substances

  • (+)-JQ1 compound
  • Azepines
  • BRD4 protein, human
  • Cell Cycle Proteins
  • Chromatin
  • Nuclear Proteins
  • Proto-Oncogene Proteins c-myb
  • Transcription Factors
  • Triazoles
  • Jumonji Domain-Containing Histone Demethylases
  • KDM6B protein, human