Am. Rijken et al., Genomic alterations in distal bile duet carcinoma by comparative genomic hybridization and karyotype analysis, GENE CHROM, 26(3), 1999, pp. 185-191
We report genomic abnormalities identified in 14 human primary common bile
duct carcinomas analyzed by cytogenetics or comparative genomic hybridizati
on, or both. Combining the results of the two methods of analysis, 11 chrom
osomal arms were observed to be gained in whole or in part, and 9 chromosom
al arms were lost in whole or in part in at least four tumors each. The mos
t frequently lost chromosomal regions were, in decreasing order: 18q (eight
tumors); 6q and 10p (seven tumors each); 8p, 12q, and 17p (six tumors each
); and 7q, 12p, and 22q (four tumors each). The most frequently gained regi
ons were 8q and 20q (six tumors each); 12p, 17q, and Xp (five tumors each);
and 2q, 6p, 7p, 11q, 13q, and 19q (four tumors each). These results are si
milar to those we have previously reported in pancreatic cancer and suggest
that carcinomas of the common bile duct and pancreas share a number of gen
etic changes. (C) 1999 Wiley-Liss, Inc.