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Genetic inactivation of the APC gene contributes to the malignant progression of sporadic hepatocellular carcinoma: A case report
Author(s) -
Katoh Hiroto,
Shibata Tatsuhiro,
Kokubu Akiko,
Ojima Hidenori,
Kosuge Tomoo,
Kanai Yae,
Hirohashi Setsuo
Publication year - 2006
Publication title -
genes, chromosomes and cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.754
H-Index - 119
eISSN - 1098-2264
pISSN - 1045-2257
DOI - 10.1002/gcc.20362
Subject(s) - biology , adenomatous polyposis coli , cancer research , wnt signaling pathway , gene , comparative genomic hybridization , locus (genetics) , hepatocellular carcinoma , nonsense mutation , genetics , tumor progression , familial adenomatous polyposis , mutation , microbiology and biotechnology , cancer , genome , colorectal cancer , missense mutation
Although activated Wnt/β‐catenin pathway is considered to be one of the main driving forces of hepatocarcinogenesis, no somatic mutations of the adenomatous polyposis coli ( APC ) gene have been found in sporadic hepatocellular carcinoma (HCC) to date. Here we present a case of a sporadic nodule‐in‐nodule‐type HCC that provides the first evidence that biallelic genetic inactivation of the APC gene contributed to the development of the tumor. High‐density array‐based comparative genomic hybridization (aCGH) was performed to clarify genome‐wide chromosomal structural alteration profiles of both early and advanced components of this nodule‐in‐nodule HCC. aCGH analysis revealed a chromosomal loss of the APC gene locus only in the inner advanced component of this tumor. Direct sequencing of the remaining allele revealed a nonsense mutation at codon 682 in the Armadillo repeats, resulting in a truncated protein that lacked all of the β‐catenin‐binding motifs. Nonsense mutations at this location are rare among other types of cancer. In conclusion, combined with an immunohistochemical analysis of the β‐catenin protein, this case provides the first evidence that genetic inactivation of the APC gene can play a significant role in the progression of sporadic HCC, probably by activating the Wnt/β‐catenin pathway. © 2006 Wiley‐Liss, Inc.