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Benzo[a]pyrene, Aflatoxine B(1) and Acetaldehyde Mutational Patterns in TP53 Gene Using a Functional Assay: Relevance to Human Cancer Aetiology

Mutations in the TP53 gene are the most common alterations in human tumours. TP53 mutational patterns have sometimes been linked to carcinogen exposure. In hepatocellular carcinoma, a specific G>T transversion on codon 249 is classically described as a fingerprint of aflatoxin B(1) exposure. Like...

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Autores principales: Paget, Vincent, Lechevrel, Mathilde, André, Véronique, Le Goff, Jérémie, Pottier, Didier, Billet, Sylvain, Garçon, Guillaume, Shirali, Pirouz, Sichel, François
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3272023/
https://www.ncbi.nlm.nih.gov/pubmed/22319594
http://dx.doi.org/10.1371/journal.pone.0030921
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author Paget, Vincent
Lechevrel, Mathilde
André, Véronique
Le Goff, Jérémie
Pottier, Didier
Billet, Sylvain
Garçon, Guillaume
Shirali, Pirouz
Sichel, François
author_facet Paget, Vincent
Lechevrel, Mathilde
André, Véronique
Le Goff, Jérémie
Pottier, Didier
Billet, Sylvain
Garçon, Guillaume
Shirali, Pirouz
Sichel, François
author_sort Paget, Vincent
collection PubMed
description Mutations in the TP53 gene are the most common alterations in human tumours. TP53 mutational patterns have sometimes been linked to carcinogen exposure. In hepatocellular carcinoma, a specific G>T transversion on codon 249 is classically described as a fingerprint of aflatoxin B(1) exposure. Likewise G>T transversions in codons 157 and 158 have been related to tobacco exposure in human lung cancers. However, controversies remain about the interpretation of TP53 mutational pattern in tumours as the fingerprint of genotoxin exposure. By using a functional assay, the Functional Analysis of Separated Alleles in Yeast (FASAY), the present study depicts the mutational pattern of TP53 in normal human fibroblasts after in vitro exposure to well-known carcinogens: benzo[a]pyrene, aflatoxin B(1) and acetaldehyde. These in vitro patterns of mutations were then compared to those found in human tumours by using the IARC database of TP53 mutations. The results show that the TP53 mutational patterns found in human tumours can be only partly ascribed to genotoxin exposure. A complex interplay between the functional impact of the mutations on p53 phenotype and the cancer natural history may affect these patterns. However, our results strongly support that genotoxins exposure plays a major role in the aetiology of the considered cancers.
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spelling pubmed-32720232012-02-08 Benzo[a]pyrene, Aflatoxine B(1) and Acetaldehyde Mutational Patterns in TP53 Gene Using a Functional Assay: Relevance to Human Cancer Aetiology Paget, Vincent Lechevrel, Mathilde André, Véronique Le Goff, Jérémie Pottier, Didier Billet, Sylvain Garçon, Guillaume Shirali, Pirouz Sichel, François PLoS One Research Article Mutations in the TP53 gene are the most common alterations in human tumours. TP53 mutational patterns have sometimes been linked to carcinogen exposure. In hepatocellular carcinoma, a specific G>T transversion on codon 249 is classically described as a fingerprint of aflatoxin B(1) exposure. Likewise G>T transversions in codons 157 and 158 have been related to tobacco exposure in human lung cancers. However, controversies remain about the interpretation of TP53 mutational pattern in tumours as the fingerprint of genotoxin exposure. By using a functional assay, the Functional Analysis of Separated Alleles in Yeast (FASAY), the present study depicts the mutational pattern of TP53 in normal human fibroblasts after in vitro exposure to well-known carcinogens: benzo[a]pyrene, aflatoxin B(1) and acetaldehyde. These in vitro patterns of mutations were then compared to those found in human tumours by using the IARC database of TP53 mutations. The results show that the TP53 mutational patterns found in human tumours can be only partly ascribed to genotoxin exposure. A complex interplay between the functional impact of the mutations on p53 phenotype and the cancer natural history may affect these patterns. However, our results strongly support that genotoxins exposure plays a major role in the aetiology of the considered cancers. Public Library of Science 2012-02-03 /pmc/articles/PMC3272023/ /pubmed/22319594 http://dx.doi.org/10.1371/journal.pone.0030921 Text en Paget et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Paget, Vincent
Lechevrel, Mathilde
André, Véronique
Le Goff, Jérémie
Pottier, Didier
Billet, Sylvain
Garçon, Guillaume
Shirali, Pirouz
Sichel, François
Benzo[a]pyrene, Aflatoxine B(1) and Acetaldehyde Mutational Patterns in TP53 Gene Using a Functional Assay: Relevance to Human Cancer Aetiology
title Benzo[a]pyrene, Aflatoxine B(1) and Acetaldehyde Mutational Patterns in TP53 Gene Using a Functional Assay: Relevance to Human Cancer Aetiology
title_full Benzo[a]pyrene, Aflatoxine B(1) and Acetaldehyde Mutational Patterns in TP53 Gene Using a Functional Assay: Relevance to Human Cancer Aetiology
title_fullStr Benzo[a]pyrene, Aflatoxine B(1) and Acetaldehyde Mutational Patterns in TP53 Gene Using a Functional Assay: Relevance to Human Cancer Aetiology
title_full_unstemmed Benzo[a]pyrene, Aflatoxine B(1) and Acetaldehyde Mutational Patterns in TP53 Gene Using a Functional Assay: Relevance to Human Cancer Aetiology
title_short Benzo[a]pyrene, Aflatoxine B(1) and Acetaldehyde Mutational Patterns in TP53 Gene Using a Functional Assay: Relevance to Human Cancer Aetiology
title_sort benzo[a]pyrene, aflatoxine b(1) and acetaldehyde mutational patterns in tp53 gene using a functional assay: relevance to human cancer aetiology
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3272023/
https://www.ncbi.nlm.nih.gov/pubmed/22319594
http://dx.doi.org/10.1371/journal.pone.0030921
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