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[Cancer Research 60, 5913-5915, November 1, 2000]
© 2000 American Association for Cancer Research


Advances in Brief

NAD(P)H:Quinone Oxidoreductase 1 Deficiency Increases Susceptibility to Benzo(a)pyrene-induced Mouse Skin Carcinogenesis1

Delwin J. Long, II, Rebekah L. Waikel, Xiao-Jing Wang, Laszlo Perlaky, Dennis R. Roop and Anil K. Jaiswal2

Departments of Pharmacology [D. J. L., A. K. J.], Molecular and Cellular Biology [R. L. W., D. R. R.], Dermatology [X-J. W.], and Pediatrics [L. P.], Baylor College of Medicine, Houston, Texas 77030

NAD(P)H:quinone oxidoreductase 1 (NQO1) is a flavoprotein that catalyzes the metabolic detoxification of quinones and their derivatives. This protects cells against quinone-induced oxidative stress, cytotoxicity, and mutagenicity. C57BL6 NQO1-/- mice, deficient in NQO1 RNA and protein, were generated in our laboratory. To investigate the role of NQO1 in chemical carcinogenesis, the dorsal skin of NQO1-deficient (NQO1-/-) and wild-type (NQO1+/+) mice were treated with a single dose of benzo(a)pyrene, followed by twice weekly applications of phorbol-12-myristate-13-acetate. The NQO1-/- mice showed a much higher frequency of skin tumor development when compared with their wild-type littermates. Interestingly, the male NQO1-/- mice were slower to develop skin tumors than their NQO1-/- female littermates. Histological analysis of the NQO1-/- tumors showed proliferative activity. These results demonstrate that NQO1 acts as an endogenous factor in protection against benzo(a)pyrene carcinogenicity.




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