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Environmental Health Perspectives (EHP) is a monthly journal of peer-reviewed research and news on the impact of the environment on human health. EHP is published by the National Institute of Environmental Health Sciences and its content is free online. Print issues are available by paid subscription.DISCLAIMER
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Environmental Health Perspectives Volume 112, Number 5, April 2004 Open Access
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Arsenic-Induced Enhancement of Ultraviolet Radiation Carcinogenesis in Mouse Skin: A Dose-Response Study

Fredric J. Burns, Ahmed N. Uddin, Feng Wu, Arthur Nádas, and Toby G. Rossman

Department of Environmental Medicine, School of Medicine, New York University, Tuxedo, New York, USA

Abstract
The present study was designed to establish the form of the dose-response relationship for dietary sodium arsenite as a co-carcinogen with ultraviolet radiation (UVR) in a mouse skin model. Hairless mice (strain Skh1) were fed sodium arsenite continuously in drinking water starting at 21 days of age at concentrations of 0.0, 1.25, 2.5, 5.0, and 10 mg/L. At 42 days of age, solar spectrum UVR exposures were applied three times weekly to the dorsal skin at 1.0 kJ/m2 per exposure until the experiment ended at 182 days. Untreated mice and mice fed only arsenite developed no tumors. In the remaining groups a total of 322 locally invasive squamous carcinomas occurred. The carcinoma yield in mice exposed only to UVR was 2.4 ± 0.5 cancers/mouse at 182 days. Dietary arsenite markedly enhanced the UVR-induced cancer yield in a pattern consistent with linearity up to a peak of 11.1 ± 1.0 cancers/mouse at 5.0 mg/L arsenite, representing a peak enhancement ratio of 4.63 ± 1.05. A decline occurred to 6.8 ± 0.8 cancers/mouse at 10.0 mg/L arsenite. New cancer rates exhibited a consistent-with-linear dependence on time beginning after initial cancer-free intervals ranging between 88 and 95 days. Epidermal hyperplasia was elevated by arsenite alone and UVR alone and was greater than additive for the combined exposures as were growth rates of the cancers. These results demonstrate the usefulness of a new animal model for studying the carcinogenic action of dietary arsenite on skin exposed to UVR and should contribute to understanding how to make use of animal data for assessment of human cancer risks in tissues exposed to mixtures of carcinogens and cancer-enhancing agents. Key words: , , , , , , , , . Environ Health Perspect 112:599-603 (2004) . doi:10.1289/ehp.6655 available via http://dx.doi.org/ [Online 6 January 2004]


Address correspondence to F.J. Burns, New York University, School of Medicine, Department of Environmental Medicine, 57 Old Forge Rd., Tuxedo, NY 10987 USA. Telephone: (845) 731-3551. Fax: (845) 351-5476. E-mail: burns@env.med.nyu.edu

We thank M. Bosland for histologic diagnoses of the tumors and D. Gray and E. Cordisco for help with manuscript preparation.

This work was supported by National Institute of Environmental Health Sciences (NIEHS) grants ES09252 and ES10344 and is part of the Nelson Institute of Environmental Medicine and the Kaplan Cancer Center programs supported by grant CA16087 from the National Cancer Institute and center grant ES00260 from the NIEHS. A.N.U. was supported by a postdoctoral fellowship from the Cancer Research and Prevention Foundation, formerly known as the Cancer Research Foundation of America.

The authors declare they have no competing financial interests.

Received 12 August 2003 ; accepted 6 January 2004.


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