Prevalence of Barrett's esophagus and expression of mucin antigens detected by a panel of monoclonal antibodies in Barrett's esophagus and esophagealadenocarcinoma in Japan
N. Azuma et al., Prevalence of Barrett's esophagus and expression of mucin antigens detected by a panel of monoclonal antibodies in Barrett's esophagus and esophagealadenocarcinoma in Japan, J GASTRO, 35(8), 2000, pp. 583-592
Barrett's esophagus (BE) is an acquired disorder associated with a high inc
idence of adenocarcinoma of the lower esophagus. Moreover, it has been repo
rted that short-segment BE may be associated with adenocarcinoma of the eso
phagogastric junction. The objective of this study was to define the preval
ence of BE and the mucin profile in BE, including the short-segment type, a
nd to compare the mucin profile in BE with the profiles of Barrett's adenoc
arcinoma and distal esophageal adenocarcinoma among Japanese. In total, 650
adult subjects underwent endoscopic examination for evaluation of BE. Alth
ough the prevalence of traditional (long segment) BE was 0.62%, the overall
prevalence of BE including short-segment type was 15.7%. In Barrett's epit
helium, the short-segment type predominantly had gastric type mucin, while
the middle- and long-segment types possessed intestinal mucin, especially c
olonic type mucin (sulfo-Lewis(a)), with high frequency. In Barrett's epith
elium with adenocarcinoma, all Barrett's epithelium adjacent to carcinomas
showed a predominance of immunoreactivity to sulfo-Lewis(a). In Barrett's a
denocarcinomas, colonic type mucin was detected in 100% by monoclonal antib
ody (MoAb) 91.9H. Small-intestinal mucin and gastric mucin were stained in
50% and 12.5% of the subjects, respectively. Colonic type mucin was also de
tected with high frequency (80%) in distal esophageal adenocarcinomas witho
ut Barrett's epithelium. These data suggest that the epitope, not of small-
intestinal type or gastric type mucin, but of colonic type mucin (sulfo-Lew
is(a)), may be associated with, at least in part, the malignant phenotype o
f BE.