Factors that contribute to faecal cyclooxygenase-2 mRNA expression in subjects with colorectal cancer

Br J Cancer. 2010 Mar 2;102(5):916-21. doi: 10.1038/sj.bjc.6605564. Epub 2010 Feb 9.

Abstract

Background: We previously reported that a faecal cyclooxygenase-2 (COX-2) mRNA assay was useful for identifying colorectal cancer (CRC). This study sought to investigate the factors that contribute to faecal COX-2 mRNA expression in subjects with CRC.

Methods: The study cohort comprised 78 patients with CRC and 36 control subjects. The expressions of COX-2, beta-2-microglobulin (B2M), carcinoembryonic antigen (CEA), E-cadherin (E-cad), and CD45 mRNA in faeces and COX-2 mRNA expression in tissue were determined by quantitative real-time RT-PCR.

Results: The level of faecal expression of COX-2 mRNA in CRC was significantly higher than that in controls. A significant correlation was found between faecal COX-2 mRNA expression and faecal B2M, CEA, E-cad, or CD45 mRNAs, markers of exfoliated total cells, colonocytes, and leukocytes, respectively. A significant correlation was found between the expression of COX-2 mRNA in faeces and tumour surface area, COX-2 mRNA expression in primary tumour. There was no difference in faecal COX-2 mRNA expression between proximal CRC and distal CRC.

Conclusion: COX-2 mRNA expression in faeces seems to originate from tumour lesion and to be affected by factors such as the number of exfoliated cells, exfoliation of inflammatory cells, COX-2 mRNA expression in tumour, and tumour size.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Biomarkers, Tumor / metabolism
  • Cadherins / genetics
  • Cadherins / metabolism
  • Carcinoembryonic Antigen / genetics
  • Carcinoembryonic Antigen / metabolism
  • Case-Control Studies
  • Cohort Studies
  • Colon / metabolism
  • Colon / pathology
  • Colorectal Neoplasms / genetics*
  • Colorectal Neoplasms / metabolism
  • Colorectal Neoplasms / pathology*
  • Cyclooxygenase 2 / genetics*
  • Cyclooxygenase 2 / metabolism
  • Feces / chemistry*
  • Female
  • Humans
  • Male
  • Middle Aged
  • Prognosis
  • RNA, Messenger / genetics*
  • RNA, Messenger / metabolism
  • Rectum / metabolism
  • Rectum / pathology
  • Reverse Transcriptase Polymerase Chain Reaction
  • Survival Rate
  • Young Adult
  • beta 2-Microglobulin / genetics
  • beta 2-Microglobulin / metabolism

Substances

  • Biomarkers, Tumor
  • Cadherins
  • Carcinoembryonic Antigen
  • RNA, Messenger
  • beta 2-Microglobulin
  • Cyclooxygenase 2
  • PTGS2 protein, human