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In vitro evaluation of the carcinogenic potential of perfluorinated chemicals

致癌物 环境化学 体外 化学 环境科学 有机化学 生物化学
作者
Monica Vaccari,Stefania Serra,Andrea Ranzi,Federico Aldrovandi,Giangabriele Maffei,Maria Grazia Mascolo,Ada Mescoli,Elisa Montanari,Gelsomina Pillo,Francesca Rotondo,Ivan Scaroni,Lorenzo Vaccari,Cristina Zanzi,Tony Fletcher,Martin Paparella,Annamaria Colacci
出处
期刊:Alternatives to animal experimentation [Springer Nature]
被引量:2
标识
DOI:10.14573/altex.2310281
摘要

Perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA) are the major components of long-chain per- and polyfluorinated alkyl substances (PFAS), known for their chemical stability and environmental persistence. Even if PFOA and PFOS have been phased out or are limited in use, they still represent a concern for human and environmental health. Several studies have been per­formed to highlight the toxicological behavior of these chemicals and their mode of action (MoA). Data have suggested a causal association between PFOA or PFOS exposure and carcinogenicity in humans, but the outcomes of epidemiological studies showed some inconsistency. Moreover, the hypothesized MoA based on animal studies is considered not relevant for human cancer. To improve the knowledge on PFAS toxicology and contribute to the weight of evidence for the regu­latory classification of PFAS, we used the BALB/c 3T3 cell transformation assay (CTA), an in vitro model under consideration to be included in an integrated approach to testing and assessment for non-genotoxic carcinogens (NGTxCs). PFOS and PFOA were tested at several concentrations using a validated experimental protocol. Our results demonstrate that PFOA does not induce cell transformation, whereas PFOS exposure induced a concentration-related increase of type III foci. Malignant foci formation was triggered at PFOS concentrations equal to or higher than 50 ppm and was not directly associated with cytotoxicity or proliferation induction. The divergent CTA outcomes suggest that different molecular events could be responsible for the toxicological profiles of PFOS and PFOA, which were not fully captured in our study.
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