Barrett esophagus (BE) is a condition in which the normal squamous epitheli
um of the esophagus is replaced by a metaplastic columnar epithelium. BE is
a premalignant lesion that represents the initial step in a metaplasia-dys
plasia-carcinoma sequence. In the present study, amplification of the proto
-oncogene c-myc was determined by means of differential polymerase chain re
action analysis of metaplastic specialized epithelium, low grade dysplasia,
high-grade dysplasia, and invasive adenocarcinoma obtained by microscopic
dissection of 43 esophagectomy specimens. Amplification of c-myc was found
in none of 29 specialized epithelial specimens, none of 23 low-grade dyspla
sia specimens, 6 of 24 high-grade dysplasia specimens, and 17 of 39 adenoca
rcinoma specimens. Our data indicate that amplification of c-myc is a late
event in the metaplasia-dysplasia-carcinoma sequence in BE. Furthermore, de
termination of c-myc amplification may help identify high-risk patients who
would benefit from intensified endoscopic surveillance or from immediate t
reatment.