| Literature DB >> 6288281 |
Abstract
Cells from 50-55 day old virgin Sprague-Dawley female rat mammary gland were divided into parenchymal (epithelial) and stromal enriched populations. The ability of these cells to activate carcinogens was quantitated employing a mediated mutagenesis assay. In addition, the populations' ability to produce water soluble metabolites from these carcinogens was estimated. We report that the potent mammary carcinogen 7,12-dimethylbenz[a]anthracene was activated by both mammary parenchymal and stromal cells, while the non-mammary carcinogen aflatoxin B1 was not activated by either cell type. However, the weak mammary carcinogen benzo[a]pyrene was activated by the stromal cells and not by the parenchymal cells from which mammary carcinomas arise. The data suggest that the intra-organ relationship between cell types that activate a carcinogen, and cell types that undergo neoplastic transformation, may in part help explain the organ specific potency of a carcinogen.Entities:
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Year: 1982 PMID: 6288281 DOI: 10.1093/carcin/3.6.667
Source DB: PubMed Journal: Carcinogenesis ISSN: 0143-3334 Impact factor: 4.944