Chromosome instability in human hepatocellular carcinoma depends on p53 status and aflatoxin exposure

Pascal Pineau, Agnès Marchio, Carlo Battiston, Emilie Cordina, Alessandro Russo, Benoît Terris, Lun Xiu Qin, Bruno Turlin, Zhao You Tang, Vincenzo Mazzaferro, Anne Dejean

Research output: Contribution to journalArticle

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Abstract

Hepatocellular carcinoma (HCC) is a heterogeneous disease triggered by various risk factors and frequently characterized by chromosome instability. This instability is considered to be caused primarily by Hepatitis B virus (HBV), although aflatoxin B1 (AFB1), a potent fungal mutagen is also suspected to influence chromosomal repair. We studied 90 HCCs from Italy, the country with the highest incidence of hepatocellular carcinoma in Europe, 81 samples from France and 52 specimens from Shanghai, in a region where intake of AFB1 via the diet is known to be high. All 223 tumours were characterized for 15 different genomic targets, including allelic loss at 13 chromosome arms and mutations of β-catenin and p53 genes. Despite disparity in risk-factor distribution, Italian and French cases did not significantly differ for 14 of the 15 targets tested. β-Catenin and p53 displayed moderate and similar mutation rates (18-29% of cases) in European series. By contrast, tumours from Shanghai were significantly different, with a lower mutation rate for β-catenin (4% vs. 26%, p <0.0003) and a higher mutation rate for p53 (48% vs. 22%, p <0.0001) when compared with tumours of European origin. The Arg249Ser mutation, hallmark of exposure to AFB1, represented half of the changes in p53 in Shanghai. Furthermore, when stratified for the presence of HBV or p53 mutations, chromosome instability was always higher in Chinese than in European patients. This difference was particularly strong in p53-wildtype tumours (fractional allelic loss, 29.4% vs. 16.7%, p <0.0001). We suggest that AFB1-associated mutagenesis represents a plausible cause for the higher chromosome instability observed in Chinese HCCs, when compared with European primary liver carcinomas.

Original languageEnglish
Pages (from-to)6-13
Number of pages8
JournalMutation Research - Genetic Toxicology and Environmental Mutagenesis
Volume653
Issue number1-2
DOIs
Publication statusPublished - May 31 2008

Fingerprint

Chromosomal Instability
Aflatoxin B1
Aflatoxins
Catenins
Hepatocellular Carcinoma
Mutation Rate
Loss of Heterozygosity
Hepatitis B virus
Mutation
Neoplasms
Chromosomes, Human, Pair 13
p53 Genes
Mutagens
Mutagenesis
Italy
France
Diet
Carcinoma
Liver
Incidence

Keywords

  • β-Catenin
  • Aflatoxin B1
  • Chromosome instability
  • Hepatitis viruses
  • Hepatocellular carcinoma
  • p53

ASJC Scopus subject areas

  • Health, Toxicology and Mutagenesis
  • Genetics
  • Molecular Biology

Cite this

Chromosome instability in human hepatocellular carcinoma depends on p53 status and aflatoxin exposure. / Pineau, Pascal; Marchio, Agnès; Battiston, Carlo; Cordina, Emilie; Russo, Alessandro; Terris, Benoît; Qin, Lun Xiu; Turlin, Bruno; Tang, Zhao You; Mazzaferro, Vincenzo; Dejean, Anne.

In: Mutation Research - Genetic Toxicology and Environmental Mutagenesis, Vol. 653, No. 1-2, 31.05.2008, p. 6-13.

Research output: Contribution to journalArticle

Pineau, Pascal ; Marchio, Agnès ; Battiston, Carlo ; Cordina, Emilie ; Russo, Alessandro ; Terris, Benoît ; Qin, Lun Xiu ; Turlin, Bruno ; Tang, Zhao You ; Mazzaferro, Vincenzo ; Dejean, Anne. / Chromosome instability in human hepatocellular carcinoma depends on p53 status and aflatoxin exposure. In: Mutation Research - Genetic Toxicology and Environmental Mutagenesis. 2008 ; Vol. 653, No. 1-2. pp. 6-13.
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AU - Terris, Benoît

AU - Qin, Lun Xiu

AU - Turlin, Bruno

AU - Tang, Zhao You

AU - Mazzaferro, Vincenzo

AU - Dejean, Anne

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