A. Kokkola et al., 17Q12-21 AMPLICON, A NOVEL RECURRENT GENETIC CHANGE IN INTESTINAL-TYPE OF GASTRIC-CARCINOMA - A COMPARATIVE GENOMIC HYBRIDIZATION STUDY, Genes, chromosomes & cancer, 20(1), 1997, pp. 38-43
We studied DNA copy number changes in gastric cancer (GC) using compar
ative genomic hybridization (CGH) analysis on 35 resected gastric carc
inomas (22 of the intestinal type and 13 of the diffuse type). Eighty-
three percent of the cases showed DNA copy number changes. Gains were
more common than losses (median of 3 and I in primary tumors of the in
testinal and diffuse type, respectively). The most common gains were d
etected on 20q [46%; 12 intestinal type (55%) and four diffuse type (3
1%)], 8q [37%; 10 intestinal type (45%) and three diffuse type (23%)],
and 17q12-21 [29%; all but one intestinal type (41%)]. The most frequ
ent losses were detected on 18q [26%; all intestinal type (41%)] and o
n 4q [23%; all intestinal type (32%)]. High-level amplifications were
observed in the intestinal type of tumors at 17q12-21 (three tumors),
20q (three tumors), 2p (one tumor), and 18q (one tumor). In the diffus
e type, high-level amplification was detected once at 13q. (C) 1997 Wi
ley-Liss, Inc.