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

Citation
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
Citations number
26
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
CARCINOGENESIS
ISSN journal
01433334 → ACNP
Volume
20
Issue
6
Year of publication
1999
Pages
1103 - 1106
Database
ISI
SICI code
0143-3334(199906)20:6<1103:MIBBIL>2.0.ZU;2-Y
Abstract
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.