Nitrated polycyclic aromatic hydrocarbons (nitro-PAHs) are formed during incomplete combustion.Sources include emissions from vehicles (mainly diesel vehicles), heating, smoking, certain types of food processing, and incomplete combustion in general.Nitro-PAHs are direct-acting mutagens, and a number of them have been shown to be carcinogens. 2-Nitrofluorene (NF) represents a model substance for the nitro-PAHs.An attempt has been made to calculate the human cancer risk due to exposure to nitro-PAHs by two different models.In the first model, genotoxic lesions were transferred to units of Gray (y-irradiation), and in the second model a mega study (24,000 animals) on the carcinogenicity of one metabolite of NF was used to elucidate the risk.Gamma-irradiation of the rat liver gave rise to preneoplastic foci in a dose-dependent manner.which was statistically significant.The Gray-equivalents of chemically (NF) induced foci were calculated, and from the human nitro-PAH exposure, expressed in Sievert, a human risk estimate was calculated.In the second model, an extrapolation from laboratory animals to man was performed because tumor data on 2-acety- laminofluorene (AAF), a major metabolite of NF, were available in the literature.The tumor dose-response data on AAF was linear for tested lifetime doses.The results ofboth models agreed, with a risk range of 0.15-49x 10 -i on human cancer risk for an urban citizen.
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Möller et al. (1993) studied this question.
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