Campylobacter Concisus and Its Effect on the Expression of CDX1 and COX2

Asian Pac J Cancer Prev. 2018 Nov 29;19(11):3211-3216. doi: 10.31557/APJCP.2018.19.11.3211.

Abstract

Background: Barrett’s oesophagus (BO) is a pre-malignant condition in which normal squamous epithelium of the lower oesophagus and gastresophageal junction is replaced by columnar cells and progress to oesophageal adenocarcinoma. The increase burden of oesophagus cancer morbidity and mortality worldwide make study of factors involved in the pathogenesis of BO essential. However, most of studies that examine the environmental risk factors associated with increased incidence and prevalence of BO have largely ignored the potential role of bacteria in disease aetiology. Aims: This study examined the role of Campylobacter concisus isolated from Barrett’s and adenocarcinoma patient samples as one of possible environmental factors in the progression of Barrett’s oesophagus to oesophagus adenocarcinoma. Methods: We focused on the effect of C. concisus on the expression caudal type homeobox 1 gene (CDX1) and cyclooxygenase-2 (COX-2) in three BO cell lines using quantitative real-time PCR. In addition, the attachment and invasion characteristics of C. concisus were also tested. Results: Results showed that C. concisus had a strong attachment to the cell lines and induce the expression of CDX1 in Barrett’s cell lines in a time-dependent manner. Conclusion: Findings indicate that C. concisus could be as a new challenge in the progression of BO to adenocarcinoma.

Keywords: Campylobacter concisus; Barrett’s oesophagus; COX2; CDX1.

MeSH terms

  • Adenocarcinoma / etiology
  • Adenocarcinoma / metabolism
  • Adenocarcinoma / pathology
  • Barrett Esophagus / etiology
  • Barrett Esophagus / metabolism*
  • Barrett Esophagus / pathology
  • Biomarkers, Tumor / metabolism
  • Campylobacter / pathogenicity*
  • Campylobacter Infections / complications*
  • Campylobacter Infections / microbiology
  • Cyclooxygenase 2 / metabolism*
  • Esophageal Neoplasms / etiology
  • Esophageal Neoplasms / metabolism*
  • Esophageal Neoplasms / pathology
  • Esophagus / metabolism
  • Esophagus / microbiology
  • Esophagus / pathology
  • Gene Expression Regulation, Neoplastic*
  • Homeodomain Proteins / metabolism*
  • Humans
  • Tumor Cells, Cultured

Substances

  • Biomarkers, Tumor
  • CDX1 protein, human
  • Homeodomain Proteins
  • Cyclooxygenase 2
  • PTGS2 protein, human