Mutagenesis induced by benzo[a]pyrene in lacZ mouse mammary and oral tissues: comparisons with mutagenesis in other organs and relationships to previous carcinogenicity assays
W. Kosinska et al., Mutagenesis induced by benzo[a]pyrene in lacZ mouse mammary and oral tissues: comparisons with mutagenesis in other organs and relationships to previous carcinogenicity assays, CARCINOGENE, 20(6), 1999, pp. 1103-1106
Thus far, in vivo mutagenic assays have detected organ-specific effects of
benzo[alpha]pyrene (B[alpha]P) in a number of organs, but not in oral tissu
es and breast. Previous studies have shown that the mouse tongue is a targe
t for tumorigenesis induced by B[alpha]P when incorporated into feed, and p
olycyclic aromatic hydrocarbons are carcinogens in mouse mammary tissue. In
order to evaluate the capacity of the lacZ mouse in vivo mutagenesis assay
to detect mutations in these target tissues, we have measured mutagenesis
induced by B[alpha]P in breast and oral tissues. The oral tissue consisted
of either tongue or a mixture of oral tissues from several sites in the ora
l cavity, B[alpha]P was more mutagenic in breast tissue than in most other
organs tested (liver, lung and kidney) when administered at relatively high
dose by gavage, and more mutagenic than in liver, but not lung, at low dos
e. when administered in an emulsion in drinking water, B[alpha]P was more m
utagenic in oral tissues than in liver, and somewhat less mutagenic than in
lung. Regardless of dose, the mutagenic activity was greatest in colon whe
re it was much higher than in other organs. A reasonable correlation was ob
served between mutagenesis observed here and carcinogenesis in previous stu
dies although some differences were noted. To our knowledge, this represent
s the first report of in vivo mutagenesis in non-tumor mammary and oral tis
sue, and the results indicate these organs can efficiently metabolize B[alp
ha]P to genotoxic products, although some transport of active metabolites f
rom the liver cannot be ruled out. The lacZ mouse mutagenesis assay may rep
resent a shorter term alternative to carcinogenesis assays for investigatio
ns of factors affecting initiation of carcinogenesis in mammary and oral ti
ssues. However, it is less predictive of actual tumor formation.