Identification and Characterization of MYC Regulatory Elements: Links to Prostate Cancer

Abstract

Prostate cancer is the most common cancer diagnosed in males in the developed world. Genome-wide association studies (GWAS) have greatly helped in the identification of common risk variants associated with complex diseases such as cancer; routinely, these associated polymorphisms are located within gene deserts and other type of non-coding DNA. A striking example of GWAS implicating non-coding variants in the etiology of cancer can be seen on chromosome 8q24, where numerous studies have reported associations between prostate (and other) cancer and variants concentrated within a 1.2Mb gene desert. Although there are no genes within the interval, the proto-oncogene MYC lies just downstream of the gene desert, raising the possibility that the associated risk regions may harbor long-range cis-regulatory elements such as enhancers involved in the tissue-specific transcriptional regulation of MYC. To date, we have located and characterized an in vivo prostate enhancer encompassing the prostate cancer associated SNPrs6983267. Furthermore, we demonstrated that this enhancer exhibits allele-specific activity in developing and mature mouse prostates, mimicking MYC expression. Our findings help advance the field s understanding of the mechanistic reason for the overwhelming association seen between this 8q24 gene desert and prostate cancer.

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Document Details

Document Type
Technical Report
Publication Date
Sep 01, 2012
Accession Number
ADA574740

Entities

People

  • Marcelo Nobrega
  • Nora Wasserman

Organizations

  • University of Chicago

Tags

DTIC Thesaurus Topics

  • Breast Cancer
  • Cancer
  • Cell Physiological Processes
  • Cells
  • Chemistry
  • Chromosome Aberrations
  • Chromosomes
  • Colon Cancer
  • Culture Techniques
  • Diseases And Disorders
  • Epithelial Cells
  • Genetics
  • Junk Dna
  • Neoplasms
  • Peptide Growth Factors
  • Prostate Cancer
  • Urinary Tract

Fields of Study

  • Biology

Readers

  • Breast cancer cell signaling and growth regulation.
  • Molecular Genetics
  • Oncology and Biomarker-Based Cancer Detection.