Abstract |
The purpose of this study was to examine whether intracellular metallothionein (MT) protects against benzo[a]pyrene (B[a]P)-induced forestomach and lung carcinogenesis. Ten-week-old male MT-I/II null mice and wild-type mice were orally administered B[a]P at a dose of 100 or 250 mg/kg twice a week for 4 weeks. B[a]P-induced mortality was higher in the MT-I/II null mice than in the wild-type mice. The incidence of tumors in the forestomach and lung was 78.6% and 7.1% in the wild-type mice treated with 100 mg/kg B[a]P, respectively. In the MT-I/II null mice treated with B[a]P, tumor incidence in the forestomach and lung was 100% and 33.3%, respectively. The tumor area in the forestomach and lung in the MT-I/II null mice treated with B[a]P was greater than that of wild-type mice. These results suggest that MT acts as a biological protective factor against carcinogenesis induced by B[a]P.
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Authors | Masaki Takaishi, Akinori Shimada, Junko S Suzuki, Masahiko Satoh, Hisamitsu Nagase |
Journal | The Journal of toxicological sciences
(J Toxicol Sci)
Vol. 35
Issue 2
Pg. 225-30
(Apr 2010)
ISSN: 1880-3989 [Electronic] Japan |
PMID | 20371973
(Publication Type: Journal Article)
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Chemical References |
- Benzo(a)pyrene
- Metallothionein
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Topics |
- Animals
- Benzo(a)pyrene
(toxicity)
- Female
- Male
- Metallothionein
(physiology)
- Mice
- Mice, Inbred C57BL
- Neoplasms, Experimental
(chemically induced, prevention & control)
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