Mutagenesis, Vol. 16, No. 4, 333-337,
July 2001
© 2001 UK Environmental Mutagen Society/Oxford University Press
Studies of dose distribution, premutagenic events and mutation frequencies for benzo[a]pyrene aiming at low dose cancer risk estimation
1 Department of Genetic and Cellular Toxicology, 2 Department of Molecular Genome Research and 3 Department of Environmental Chemistry, Stockholm University, S-106 91 Stockholm and 4 Unit for Molecular Epidemiology, Novum, Karolinska Institute, S-141 57 Huddinge, Sweden
Cancer risk assessment of polycyclic aromatic hydrocarbons (PAH) is complicated by several of these compounds exerting a promoter action leading to high tumour incidences at high doses. Cancer risks at low doses corresponding to the uptake from air and food in the general environment would best be estimated on the basis of measurement of in vivo target doses of genotoxic (mutagenic) intermediates and a determination of mutation frequency per unit of dose. In experiments ultimately aiming at a risk assessment of environmental PAH from in vivo doses benzo[a]pyrene (BaP) was chosen as a model. 
-Radiation has earlier been used as a reference standard in cancer risk estimation of genotoxic chemicals where dose equivalents (rad-equivalents) have been shown to give reliable risk estimates for several alkylating agents. Variation in dose of BaP diolepoxide between organs was studied by measurement of deoxyguanosine-N2 adducts in DNA after administration of BaP by gavage to mice of a strain with reduced DNA repair (Xpa–/–). The adduct levels in spleen, forestomach, stomach and small intestine were approximately the same; with the adduct level in spleen as reference it was twice as high in liver and lung and about half as high in colon tissue. A chemical or radiation dose is proportional to the cumulative frequency of putatively premutagenic changes (premutagenic hits) in DNA. The mutation frequency per premutagenic hit (genotoxic chemicals) and per unit of dose (-radiation) were calculated from acutely exposed V79 cells in order to determine the mutagenic effectiveness of each agent. Based on the mutagenic effectiveness determined in this study 10–4 Gy can be regarded equally effective in causing phenotypically expressed HPRT mutations as the dose of BaP which causes the formation of one deoxyguanosine-N2 adduct per cell.
5 Present address: China Institute for Radiation Protection, Taiyuan, Shanxi 030006, China
6 To whom correspondence should be addressed. Email: margareta.tornqvist{at}mk.su.se
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