Tumor-initiating activity of the dihydrodiols of 8-methylbenz-[a]anthracene and 8-hydroxymethylbenz[a]anthracene

The tumor-initiating activity of the 3, 4-dihydrodiols (diols) as well as other metabolites of 8-methylbenz[a]-anthracene (8-MBA) and 8-hydroxymethylbenz[a)-anthracene (8-OHMBA) were examined in the classical 2-stage initiation-promotion model on mouse skin. The 3,4-diol of 8-MBA caused 2.2 times as...

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Veröffentlicht in:Carcinogenesis (New York) 1981, Vol.2 (6), p.507-509
Hauptverfasser: Wislocki, Peter G., Fiorentini, Karen M., Fu, Peter P., Chou, Ming W., Yang, Shen K., Lu, Anthony Y. H.
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Sprache:eng
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Zusammenfassung:The tumor-initiating activity of the 3, 4-dihydrodiols (diols) as well as other metabolites of 8-methylbenz[a]-anthracene (8-MBA) and 8-hydroxymethylbenz[a)-anthracene (8-OHMBA) were examined in the classical 2-stage initiation-promotion model on mouse skin. The 3,4-diol of 8-MBA caused 2.2 times as many papillomas/mouse as did 8-MBA. The 3,4-diol of 8-OHMBA was not more tumorigenic than either 8-MBA or 8-OHMBA. None of the other diols tested, including the 5,6- and 8,9-diol of 8-MBA and the 5,6 and 10,11-diol of 8-OHMBA were remarkably tumor-igenic. These data indicate that the 3,4-diol of 8-MBA is a good candidate as a proximate carcinogen of 8-MBA and further suggest that the bay region 3,4-diol-1,2-epoxide is a likely ultimate carcinogen of this compound on mouse skin.
ISSN:0143-3334
1460-2180
DOI:10.1093/carcin/2.6.507