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Carcinogenesis Advance Access published online on May 25, 2005

Carcinogenesis, doi:10.1093/carcin/bgi141
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© The Author 2005. Published by Oxford University Press. All rights reserved. For permissions, please email: journals.permissions@oupjournals.org
Received March 21, 2005
Revised May 20, 2005
Accepted May 22, 2005

CARCINOGENESIS

DNA-adduct and tumor formations in rats after intratracheal administration of the urban air pollutant 3-nitrobenzanthrone

Eszter Nagy 1, Magnus Zeisig 1, Ken Kawamura 2, Yoshiharu Hisamatsu 3, Akiko Sugeta 4, Shuichi Adachi 4, and Lennart Möller 1*

1 Karolinska Institutet, Department for Biosciences at Novum, SE-141 57 Huddinge, Stockholm, Sweden
2 Department of Pathology, Kagawa Nutrition University, Sakado, Saitama 350-0288, Japan
3 Department of Community Environmental Science, National Institute of Public Health, Shirokanedai, Tokyo 108-8638, Japan
4 Department of Public Health, Sagami Women's University, Sagamihara, Kanagawa 228-8533, Japan

* To whom correspondence should be addressed.
Lennart Möller, E-mail: lennart.moller{at}biosci.ki.se


   Abstract

3-nitrobenzanthrone (3-NBA) has been isolated from diesel exhaust and airborne particles, and identified as a potent direct-acting mutagen in vitro and genotoxic agent in vivo. In order to evaluate the in vivo toxicity and carcinogenicity of 3-NBA in a situation corresponding to inhalation, a combined short-term and lifetime study with intratracheal instillation in female F344 rats was performed. DNA-adduct formation, as a marker for the primary effect and analyzed by 32P-HPLC after single instillation, showed a few major DNA-adducts and a rapid increase with a peak after 2 days, followed by a decline. No DNA-adducts above background level were observed after 16 days. The highest DNA-adduct formation was observed in lung (~250 DNA-adducts/108 normal nucleotides (NN)) closely followed by kidney (~200 DNA-adducts/108 NN), whereas liver contained only 12% (~30 DNA-adducts/108 NN) of the levels of DNA-adducts found in lung.

In the tumor study, squamous cell carcinomas were found after 7-9 months in the high dose group (total dose of 2.5 mg 3-NBA) and after 10-12 months in the low dose group (total dose of 1.5 mg 3-NBA). The fraction of squamous cell carcinoma out of the total amount of tumors observed at the end of experiment at 18 months, corresponded to 3/16 and 11/16 in the low and high dose group, respectively. A single case of adenocarcinoma was also observed in each group. In the control group, no tumors were observed during the entire study of 18 months. In addition, a few cases of squamous metaplasia were also observed in the lung in both dose groups, but not in the controls.

In conclusion, 3-NBA forms DNA-adducts in the lung immediately after intratracheal administration but almost all DNA-adducts were eliminated after 16 days. Tumor formation in two dose groups was observed in a dose-dependent manner with squamous cell carcinomas as the predominant tumor type at high exposure.

Keywords: 3-nitrobenzanthrone; diesel exhaust; intratracheal administration; F344 rat; DNA-adduct; tumor; carcinogenicity; liver; lung; kidney; adenocarcinoma; squamous cell carcinoma.
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