Use of mesothelial cell cultures to assess the carcinogenic potency of mineral or man made fibers

• Published in: Cell biology and toxicology Vol. 8; no. 3; p. 133
• Main Authors: Renier, A, Yegles, M, Buard, A, Dong, H, Kheuang, L, Saint-Etienne, L, Laurent, P, Jaurand, M C
• Format: Journal Article
• Language: English
• Published: Netherlands 01.07.1992
• Subjects: Animals; Asbestos - toxicity; Carcinogenicity Tests; Carcinogens - toxicity; Cells, Cultured; Epithelium - drug effects; Minerals - toxicity; Models, Biological
• ISSN: 0742-2091
• DOI: 10.1007/BF00130520

Natural mineral fibers may produce pulmonary cancers and mesothelioma. In contrast with lung cancer, the incidence of fiber-induced mesothelioma is not enhanced in smokers compared to non smokers. It is therefore of special interest to use mesothelial cells to study the toxicity of natural or man made mineral fibers. Several years ago, we have developed a method to culture rat pleural mesothelial cells (RPMC). We have first studied the effects of asbestos fibers by the application of in vitro tests formerly developed to determine the genotoxicity and transforming potency of soluble xenobiotics. Moreover, we have determined whether RPMC expressed cytochromes P450 known to metabolize polycyclic aromatic hydrocarbons. This paper reviews the results obtained so far. It has been found that asbestos fibers produced a cell transformation and a genotoxicity characterized by the formation of aneuploid cells, abnormal anaphases, chromosomal aberrations and DNA repair (UDS). In addition, RPMC expressed different forms of cytochromes P450. It is nowadays suggested that the tumorigenic potency of asbestos fibers may be related to the fiber dimensions, to their surface properties and in vivo biopersistence; this term involves the fiber solubility in biological medium and the fiber epuration from the lung by clearance mechanisms. Experiments are now in progress to determine whether the in vitro effects are dependent on the fiber parameters suggested as playing a role in the carcinogenic potency.