Nasopharyngeal carcinoma super-enhancer-driven ETV6 correlates with prognosis

Proc Natl Acad Sci U S A. 2017 Sep 5;114(36):9683-9688. doi: 10.1073/pnas.1705236114. Epub 2017 Aug 22.

Abstract

Nasopharyngeal carcinoma (NPC) most frequently occurs in southern China and southeast Asia. Epidemiology studies link NPC to genetic predisposition, Epstein-Barr virus (EBV) infection, and environmental factors. Genetic studies indicate that mutations in chromatin-modifying enzymes are the most frequent genetic alterations in NPC. Here, we used H3K27ac chromatin immune precipitation followed by deep sequencing (ChIP-seq) to define the NPC epigenome in primary NPC biopsies, NPC xenografts, and an NPC cell line, and compared them to immortalized normal nasopharyngeal or oral epithelial cells. We identified NPC-specific enhancers and found these enhancers were enriched with nuclear factor κB (NF-κB), IFN-responsive factor 1 (IRF1) and IRF2, and ETS family members ETS1 motifs. Normal cell-specific enhancers were enriched with basic leucine zipper family members and TP53 motifs. NPC super-enhancers with extraordinarily broad and high H3K27ac signals were also identified, and they were linked to genes important for oncogenesis including ETV6. ETV6 was also highly expressed in NPC biopsies by immunohistochemistry. High ETV6 expression correlated with a poor prognosis. Furthermore, we defined the EBV episome epigenetic landscapes in primary NPC tissue.

Keywords: ETV6; Epstein–Barr virus; H3K27ac; nasopharyngeal carcinoma; super-enhancer.

Publication types

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

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Animals
  • Azepines / pharmacology
  • Carcinoma / etiology
  • Carcinoma / genetics*
  • Carcinoma / metabolism
  • Cell Cycle Proteins
  • Cell Line, Tumor
  • ETS Translocation Variant 6 Protein
  • Enhancer Elements, Genetic* / drug effects
  • Epigenesis, Genetic
  • Epstein-Barr Virus Infections / complications
  • Female
  • Genome, Viral
  • Heterografts
  • High-Throughput Nucleotide Sequencing
  • Histone Code / genetics
  • Humans
  • Immunohistochemistry
  • Male
  • Mice
  • Mice, Nude
  • Middle Aged
  • Nasopharyngeal Carcinoma
  • Nasopharyngeal Neoplasms / etiology
  • Nasopharyngeal Neoplasms / genetics*
  • Nasopharyngeal Neoplasms / metabolism
  • Nuclear Proteins / antagonists & inhibitors
  • Prognosis
  • Proto-Oncogene Proteins c-ets / genetics*
  • Proto-Oncogene Proteins c-ets / metabolism
  • Repressor Proteins / genetics*
  • Repressor Proteins / metabolism
  • Transcription Factors / antagonists & inhibitors
  • Triazoles / pharmacology
  • Young Adult

Substances

  • (+)-JQ1 compound
  • Azepines
  • BRD4 protein, human
  • Cell Cycle Proteins
  • Nuclear Proteins
  • Proto-Oncogene Proteins c-ets
  • Repressor Proteins
  • Transcription Factors
  • Triazoles