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PMID: 6275985 Published · ppublish English Comparative Study Journal Article Research Support, U.S. Gov't, P.H.S.

Metabolism and binding of benzo(a)pyrene and 2-acetylaminofluorene by short-term organ cultures of human and rat bladder.

Cancer research ·Vol. 42 ·No. 2 ·1982-02-00 ·Pages 642-8

Moore BP, Hicks RM, Knowles MA, Redgrave S

Abstract

The ability of organ cultures of normal human and rat bladder to metabolize the polycyclic hydrocarbon, benzo(a)pyrene (BP), and the arylamine, 2-acetylaminofluorene, has been studied. Cultures were maintained for 0 to 6 days in a chemically defined medium before incubation with [3H]BP (0.3 to 0.5 microM) or 2-[14C]acetylaminofluorene (18 to 25 microM) for 24 hr. Ethyl acetate-soluble and water-soluble metabolites were produced from both compounds by both species. The ethyl acetate extracts from [3H]BP-treated human cultures contained 9,10-dihydro-9,10-dihydroxybenzo(a)pyrene, 7,8-dihydro-7,8-dihydroxybenzo(a)pyrene, and 3-hydroxybenzo(a)pyrene. Rat bladder cultures produced similar metabolites but in slightly different proportions. Ethyl acetate-soluble products of 2-[14C]acetylaminofluorene from human cultures contained 7-hydroxy-2-acetylaminofluorene, 9-hydroxy-2-acetylaminofluorene, 2-aminofluorene, and N-hydroxy-2-aminofluorene. Rat bladder cultures produced similar metabolites, but 2-aminofluorene was found in relatively higher proportion. Hydrolysis by beta-glucuronidase of the water-soluble products produced from both carcinogens gave ethyl acetate-extractable derivatives. These hydrolyzable glucuronide conjugates were relatively more abundant following metabolism of the carcinogens by the rat than by the human cultures. Covalent binding to DNA occurred with [3H]BP in both human (19.7 +/- 13 pmol/mg DNA) and rat cultures (22.8 +/- 8.6 pmol/mg DNA). As with other human tissues, considerable variation (50-fold) was observed between individuals. The results demonstrate that both human and rat bladder epithelium can metabolize known potent carcinogens and, in the case of BP, can effect covalent binding between the products of metabolism and the urothelial cell DNA. In theory, carcinogenesis in the urinary bladder could thus be initiated by carcinogens produced or excreted in the urine without the necessity for their prior metabolism elsewhere in the body.

MeSH Terms
2-Acetylaminofluorene/metabolism Animals Benzo(a)pyrene Benzopyrenes/metabolism DNA/metabolism Dihydroxydihydrobenzopyrenes Epithelium/metabolism Female Glucuronidase Humans Hydroxyacetylaminofluorene/metabolism Male Organ Culture Techniques Rats Urinary Bladder/metabolism
Chemicals
Benzopyrenes Dihydroxydihydrobenzopyrenes 9,10-dihydro-9,10-dihydroxybenzo(a)pyrene Benzo(a)pyrene Hydroxyacetylaminofluorene 3-hydroxybenzo(a)pyrene DNA 2-Acetylaminofluorene Glucuronidase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Moore B P
Hicks R M
Knowles M A
Redgrave S
Article Info
Journal
Cancer research
Abbr.
Cancer Res
ISSN
0008-5472
Published
1982-02-00
Pages
642-8
Language
English
Region
United States
NLM ID
2984705R
Subset
IM
Grants
NCI NIH HHS · N01 CP 75955 · United States
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