An analysis of genetic factors related to risk of inflammatory bowel disease and colon cancer

Cancer Epidemiol. 2014 Oct;38(5):583-90. doi: 10.1016/j.canep.2014.07.003. Epub 2014 Aug 15.

Abstract

Background and aims: Patients with inflammatory bowel disease (IBD) have a higher risk of developing colorectal cancer than the general population. Genome-wide association studies have identified and replicated several loci associated with risk of IBD; however, it is currently unknown whether these loci are also associated with colon cancer risk.

Methods: We selected 15 validated SNPs associated with risk of either Crohn's disease, ulcerative colitis, or both in previous GWAS and tested whether these loci were also associated with colon cancer risk in a two-stage study design.

Results: We found that rs744166 in STAT3 was associated with colon cancer risk in two studies; however, the direction of the observation was reversed in TP53 mutant tumors possibly due to a nullification of the effect by mutant p53. The SNP, which lies within intron 1 of the STAT3 gene, was associated with lower expression of STAT3 mRNA in TP53 wild-type, but not mutant, tumors.

Conclusions: These data suggest that the STAT3 locus is associated with both IBD and cancer. Further understanding the function of this variant in relation to TP53 could possibly explain the role of this gene in autoimmunity and cancer. Furthermore, an analysis of this locus, specifically in a population with IBD, could help to resolve the relationship between this SNP and cancer.

Keywords: Colon cancer; Inflammatory bowel disease; STAT3.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Aged
  • Case-Control Studies
  • Colitis, Ulcerative / complications
  • Colitis, Ulcerative / genetics*
  • Colonic Neoplasms / etiology
  • Colonic Neoplasms / genetics*
  • Crohn Disease / complications
  • Crohn Disease / genetics*
  • Female
  • Genetic Predisposition to Disease
  • Genome-Wide Association Study
  • Humans
  • Male
  • Middle Aged
  • Polymorphism, Single Nucleotide
  • RNA, Messenger / metabolism
  • STAT3 Transcription Factor / genetics*

Substances

  • RNA, Messenger
  • STAT3 Transcription Factor