In order to identify the significant allelic loss involving the gastric ade
noma-carcinoma sequence, we used 49 genome-wide microsatellite markers in a
n allelotype study of 30 cases of stomach resections that harbored both ade
nomas and carcinomas. Frequent loss of heterozygosity was demonstrated on 1
2q (53.3%), 2p (50.0%), and 18p (50.0%) in adenomas and on 8q (80.0%), 2p (
70.0%), 18p (66.7%), and 17p (61.9%) in carcinomas. Significant difference
in the loss of heterozygosity rate between the adenoma and the carcinoma wa
s noted on 17p. Our results suggested that the critical target of loss of h
eterozygosity in gastric adenoma-carcinoma sequences may be the p53 gene on
17p.