We examined the genomic status of the p16(INK4A) (inhibitor of cyclin-
dependent kinase 4 A) and cyclin dependent kinase 4 (CDK4) genes in 62
human hepatocellular carcinomas (HCCs), 5 cholangiocellular carcinoma
s and 6 cell lines derived from human liver cancers, Although no sampl
es showed the homozygous deletion of the p16(INK4A) gene, we detected
intragenic mutations of the p16(INK4A) gene in 3 HCCs and one HCC cell
line, which led to an amino-acid substitution or a frameshift. In 2 H
CC samples with mis-sense mutations of the p16(INK4A) gene, loss of he
terozygosity on 9p22 was also detected, suggesting that the loss of fu
nction of p16 was induced during hepatocarcinoegenesis. On the other h
and, amplification or rearrangement of the CDK4 gene was not detected
in any samples examined in this study. These results indicated that th
e mutations or deletions of the p16(INK4A) gene are not frequent, but
may play a role in a sob-set of human HCC. (C) 1996 Wiley-Liss, Inc.