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Carcinogenicity of benzo(a)pyrene and thirteen of its derivatives in C3H/fCum mice

Journal Article · · J. Natl. Cancer Inst.; (United States)
OSTI ID:6925662
Benzo(a)pyrene (BP) and 13 of its derivatives were tested for their ability to induce fibrosarcomas in inbred male C3H/fCum mice after a single sc injection. A 0.9-..mu..mol dose of BP in 0.05 ml dimethyl sulfoxide or 0.1 ml trioctanoin produced a 63 or 83% tumor incidence, respectively. At the same dose, benzo(a)pyrene-7,8-oxide had very weak tumorigenic activity whereas the benzo(a)pyrene-4.5-, 9.10-,and 11.12-oxides had no tumorigenic activity. When administered in dimethyl sulfoxide, (+-0-trans-7,8-dihydroxy-7,8-dihydrobenzo(a)pyrene (BP-7,8-dihydrodiol) had tumorigenic activity comparable to BP. However, the tumorigenicity of this dihydrodiol was lost when it was injected in trioctanion. The potent tumorigenicity of 7,8-dihydrobenzo(a)pyrene, compared to that of 9,10-dihydrobenzo(a)pyrene, provided evidence for the importance of an intact 9,10-double bond for the metabolic activation of BP. 2-Hydroxybenzo(a)pyrene, a potent carcinogen on mouse skin and in the newborn mouse, was only 10% as active as BP after sc injection in the mouse.
OSTI ID:
6925662
Journal Information:
J. Natl. Cancer Inst.; (United States), Journal Name: J. Natl. Cancer Inst.; (United States) Vol. 64:3; ISSN JNCIA
Country of Publication:
United States
Language:
English