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Carcinogenesis Advance Access originally published online on February 1, 2007
Carcinogenesis 2007 28(7):1599-1605; doi:10.1093/carcin/bgm023
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© The Author 2007. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Clinico-pathological features and somatic gene alterations in refractory ceramic fibre-induced murine mesothelioma reveal mineral fibre-induced mesothelioma identities

Pascal Andujar1,2, Céline Lecomte3,9, Annie Renier3,4, Jocelyne Fleury-Feith3,5,6, Laurence Kheuang1,2, Julien Daubriac3,4, Anne Janin7,8 and Marie-Claude Jaurand3,4,*

1 INSERM, U841, IMRB, Créteil, F-94000, France
2 Université Paris 12, Faculté de Médecine, IFR10, Créteil, F-94000, France
3 INSERM, U674, Fondation Jean Dausset—CEPH, IFR105, Paris, F-75010, France
4 Université Paris 7, Paris, F-75005, France
5 AP-HP, GHU Est, Hôpital Tenon, Laboratoire d'Histologie et de Biologie Tumorale, Paris, F-75020, France
6 Université Paris 6, UFR Pierre et Marie Curie, Paris, F-75012, France
7 INSERM, U728, Paris, F-75010, France
8 AP-HP, GHU Nord, Hôpital Saint-Louis, Laboratoire de Pathologie, Paris, F-75010, France
9 Present address: Université du Havre, UFR de Sciences et Techniques, UPRES-EA3222, Laboratoire d'Ecotoxicologie, Le Havre, F-76000, France

* To whom correspondence should be addressed. Tel: +33 1 53 72 51 88; Fax: +33 1 53 72 51 92; Email: jaurand{at}cephb.fr

Although human malignant mesothelioma (HMM) is mainly caused by asbestos exposure, refractory ceramic fibres (RCFs) have been classified as possibly carcinogenic to humans on the basis of their biological effects in rodents’ lung and pleura and in cultured cells. Hence, further investigations are needed to clarify the mechanism of fibre-induced carcinogenicity and to prevent use of harmful particles. In a previous study, mesotheliomas were found in hemizygous Nf2 (Nf2+/–) mice exposed to asbestos fibres, and showed similar alterations in genes at the Ink4 locus and in Trp53 as described in HMM. Here we found that Nf2+/– mice developed mesotheliomas after intra-peritoneal inoculation of a RCF sample (RCF1). Clinical features in exposed mice were similar to those observed in HMM, showing association between ascite and mesothelioma. Early passages of 12 mesothelioma cell cultures from ascites developed in RCF1-exposed Nf2+/– mice demonstrated frequent inactivation by deletion of genes at the Ink4 locus, and low rate of Trp53 point and insertion mutations. Nf2 gene was inactivated in all cultures. In most cases, co-inactivation of genes at the Ink4 locus and Nf2 was found and, at a lower rate, of Trp53 and Nf2. These results are the first to identify mutations in RCF-induced mesothelioma. They suggest that nf2 mutation is complementary of p15Ink4b, p16Ink4a and p19Arf or p53 mutations and show similar profile of gene alterations resulting from exposure to ceramic or asbestos fibres in Nf2+/– mice, also consistent with the one found in HMM. These somatic genetic changes define different pathways of mesothelial cell transformation.

Abbreviations: gDNA, genomic DNA; HMM, human malignant mesothelioma; PCR, polymerase chain reaction; RCF, refractory ceramic fibre

Received October 10, 2006; revised December 20, 2006; accepted January 13, 2007.


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