Identification and Quantification of the Depurinating DNA Adducts Formed in Mouse Skin Treated with Dibenzo[a,l]pyrene (DB[a,l]P) or Its Metabolites and in Rat Mammary Gland Treated with DB[a,l]P-Reference-Cited by-同舟云学术

Identification and Quantification of the Depurinating DNA Adducts Formed in Mouse Skin Treated with Dibenzo[a,l]pyrene (DB[a,l]P) or Its Metabolites and in Rat Mammary Gland Treated with DB[a,l]P

Published:2005-04-30 Issue:6 Volume:18 Page:976-983
ISSN:0893-228X
Container-title:Chemical Research in Toxicology
language:en
Short-container-title:Chem. Res. Toxicol.

Author:

Cavalieri Ercole L.¹,Rogan Eleanor G.¹,Li Kai-Ming¹,Todorovic Rosa¹,Ariese Freek¹,Jankowiak Ryszard¹,Grubor Nenad¹,Small Gerald J.¹

Affiliation:

1. Eppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, 986805 Nebraska Medical Center, Omaha, Nebraska 68198-6805, Ash Stevens, Inc., 5861 John C. Lodge Freeway, Detroit, Michigan 48202-3398, Department of Analytical Chemistry and Applied Spectroscopy, Laser Centre, Vrije Universiteit, De Boelelaan 1083, 1081 HV Amsterdam, The Netherlands, and Department of Chemistry, Iowa State University, Ames, Iowa 50011-3111

Publisher

American Chemical Society (ACS)

Subject

Toxicology,General Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/tx049682k

Reference46 articles.

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3. Tumor-initiating activity and carcinogenicity of dibenzo[a,l]pyrene versus 7, 12-dimethylbenz[a]anthracene and benzo[a]pyrene at low doses in mouse skin

4. Exceptional tumor-initiating activity of 4-fluorobenzo[j]-fluoranthene on mouse skin: comparison with benzo[j]-fluoranthene, 10-fluoro-benzo[j]fluoranthene, benzo[a]pyrene, dibenzo[a,l]pyrene and 7,12-dimethylbenz[a]anthracene

5. Gill, H. S., Kole, P. L., Wiley, J. C., Li, K.M., Higginbotham, S., Rogan, E. G., and Cavalieri, E. L (1994) Synthesis and tumor-initiating activity in mourse skin of dibenzo[a,l]pyrenesyn- andanti-fjord-region diolepoxides.Carcinogenesis 15, 2455−2460.

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