PEpiD: a prostate epigenetic database in mammals

PLoS One. 2013 May 16;8(5):e64289. doi: 10.1371/journal.pone.0064289. Print 2013.

Abstract

Epigenetic mechanisms play key roles in initiation and progression of prostate cancer by changing gene expression. The Prostate Epigenetic Database (PEpiD: http://wukong.tongji.edu.cn/pepid) archives the three extensively characterized epigenetic mechanisms DNA methylation, histone modification, and microRNA implicated in prostate cancer of human, mouse, and rat. PEpiD uses a distinct color scheme to present the three types of epigenetic data and provides a user-friendly interface for flexible query. The retrieved information includes Refseq ID, gene symbol, gene alias, genomic loci of epigenetic changes, tissue source, experimental method, and supportive references. The change of histone modification (hyper or hypo) and the corresponding gene expression change (up or down) are also indicated. A graphic view of DNA methylation with exon-intron structure and predicted CpG islands is provided as well. Moreover, the prostate-related ENCODE tracks (DNA methylation, histone modifications, chromatin remodelers), and other key transcription factors with reported roles in prostate are displayed in the browser as well. The reversibility of epigenetic aberrations has made them potential markers for diagnosis and prognosis, and targets for treatment of cancers. This curated information will improve our understanding of epigenetic mechanisms of gene regulation in prostate cancer, and serve as an important resource for epigenetic research in prostate cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chromatin Assembly and Disassembly / genetics
  • Chromatin Assembly and Disassembly / physiology
  • DNA Methylation / genetics
  • Databases, Genetic*
  • Epigenesis, Genetic / genetics*
  • Histones / metabolism
  • Humans
  • Male
  • Mice
  • Prostate / metabolism*
  • Rats

Substances

  • Histones

Grants and funding

This work was supported by the Ministry of Science and Technology of China [2010CB944901, 2011CB965104, 2012AA020405 to CJ]; and the National Natural Science Foundation of China [91019017, 31271373 to CJ]. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.