Ma. Collonge-rame et al., Pattern of chromosomal imbalances in non-B virus related hepatocellular carcinoma detected by comparative genomic hybridization, CANC GENET, 127(1), 2001, pp. 49-52
Only limited data are available on comparative genomic hybridization (CGH)
in hepatocellular carcinoma (HCC). They concern mainly B virus related HCC.
Therefore, we used CGH to detect chromosomal imbalances in 16 non-B virus
related HCC in alcoholic cirrhosis in 7 cases (HA1 to HA7), in C virus cirr
hosis in 7 cases (HC1 to HC7), in non-cirrhotic liver in 2 cases (NC1, NC2)
; and in 9 non-malignant cirrhotic tissues. The most frequent imbalances in
HCC were gains of whole chromosomes or chromosomal regions 7 or 7q (10/16,
62%), 1q (9/16; 56%), 5 or 5q (9/16, 56%), 8q (8/16, 50%), 6p (6/16, 37%),
15q (5/16, 31%), 20 or 20q (5/16: 31%), and losses of 17p (6/ 16, 37%), an
d Sp (5/16, 31%). High-level gains were identified in HCC on 1q (2/16), 3q
(1/16), 7q (1/16), and 8q (3/16). No chromosomal imbalances were detected i
n any of the cirrhotic tissues. Most of the gains, losses, and amplificatio
ns detected in this CGH study corresponded well to those identified in prev
ious studies, except for gains of whole chromosome 5 or 7 and/or of chromos
ome arms 5q or 7q and losses on 4q. Our results suggest that other chromoso
mal regions are involved in hepatocarcinogenesis. (C) 2001 Elsevier Science
Inc. All rights reserved.