Gastric cancer is one of the leading causes of death from cancer throughout
the world, and studies to elucidate the genetic defects found in this type
of cancer are growing in number. Increasingly sophisticated techniques and
the sequencing of the human genome have had an impact on the scope of such
studies. While the use of tumor specimens remains popular, more emphasis i
s being placed on cell lines as model systems where specific data can be di
rectly combined with results from other studies. This article describes a g
enetic survey of the most widely used gastric adenocarcinoma cell lines. Th
e allelotype at 351 polymorphic loci in 14 cell lines was obtained, and the
results from the 4,900 polymerase chain reactions are displayed. In additi
on to confirming loss of heterozygosity on chromosome arms 6p, 7q, 17p, and
18, additional deletions on arm Sp and the pericentromeric regions of chro
mosomes I and 10 were detected. Areas that might contain homozygous deletio
ns or amplifications also were mapped. The rate of microsatellite instabili
ty was quantified and shown to vary greatly among the different cell lines.
Most important, this study serves as a genetic scaffold for the integratio
n of past and future studies on the nature of the genetic defects in gastri
c cancer. (C) 2001 Wiley-Liss, Inc.