Increased expression of inducible nitric oxide synthase and cyclooxygenase-2 in Barrett's esophagus and associated adenocarcinomas

Cancer Res. 1998 Jul 15;58(14):2929-34.

Abstract

Barrett's esophagus is a premalignant condition arising in response to chronic reflux esophagitis. Inducible nitric oxide synthase (iNOS; NOS-2) and cyclooxygenase-2 (COX-2) are mediators of inflammation and regulators of epithelial cell growth. Expression levels of iNOS and COX-2 are high in colorectal adenomas and carcinomas, and COX-2 expression is elevated in gastric cancers. To determine the involvement of iNOS and COX-2 in Barrett's-associated neoplasia, we measured expression of these genes in metaplastic Barrett's and esophageal adenocarcinomas. We detected elevated iNOS and COX-2 mRNA levels in Barrett's mucosa compared with paired gastric control tissues in 16 of 21 (76%) and 17 of 21 (80%) patients, respectively (P < 0.001 for both genes). In esophageal adenocarcinomas, iNOS and COX-2 mRNA levels were increased in four of five and five of five cases, respectively. Furthermore, in 10 of 10 Barrett's patients, immunohistochemical staining for iNOS and COX-2 expression was strongly positive and higher than in matched gastric controls. Increased COX-2 expression was confirmed by Western blotting. These findings support the hypothesis that iNOS and COX-2 are involved early and often in Barrett's-associated neoplastic progression.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenocarcinoma / enzymology*
  • Adenocarcinoma / pathology
  • Barrett Esophagus / complications
  • Barrett Esophagus / enzymology*
  • Barrett Esophagus / pathology
  • Cyclooxygenase 2
  • Esophageal Neoplasms / enzymology*
  • Esophageal Neoplasms / pathology
  • Humans
  • Immunohistochemistry
  • Isoenzymes / analysis*
  • Isoenzymes / metabolism
  • Membrane Proteins
  • Neoplasm Proteins / analysis*
  • Neoplasm Proteins / metabolism
  • Nitric Oxide Synthase / analysis*
  • Nitric Oxide Synthase / metabolism
  • Prostaglandin-Endoperoxide Synthases / analysis*
  • Prostaglandin-Endoperoxide Synthases / metabolism
  • RNA, Messenger / metabolism*

Substances

  • Isoenzymes
  • Membrane Proteins
  • Neoplasm Proteins
  • RNA, Messenger
  • Nitric Oxide Synthase
  • Cyclooxygenase 2
  • PTGS2 protein, human
  • Prostaglandin-Endoperoxide Synthases