Ornithine decarboxylase induction by chemically complex liquids from two solvent refined coal processes

Studies with a variety of chemically purified substances have suggested that induction of the enzyme ornithine decarboxylase (ODC) in mouse epiderinal cells may be a reliable indicator of neoplastic transformation. In an effort to extend these observations on ODC to chemically complex materials, we...

Full description

Saved in:
Bibliographic Details
Published in:Carcinogenesis (New York) 1983, Vol.4 (7), p.805-810
Main Authors: Swanger, Dennis, Mahlum, D.Dennis, Springer, David L.
Format: Article
Language:English
Subjects:
Animals
Carboxy-Lyases - genetics
Cell Transformation, Neoplastic
Coal - adverse effects
Enzyme Induction
Female
Kinetics
Mice
Ornithine Decarboxylase - genetics
Skin - drug effects
Skin - enzymology
Solvents
Tetradecanoylphorbol Acetate - toxicity
Citations: Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Studies with a variety of chemically purified substances have suggested that induction of the enzyme ornithine decarboxylase (ODC) in mouse epiderinal cells may be a reliable indicator of neoplastic transformation. In an effort to extend these observations on ODC to chemically complex materials, we examined ODC induction by carcinogenic and non-carcinogenic mixtures and compared these results with tumorigenicity data for these materials. For these studies several boiling range fractions and several solvent-derived subfractions from two solvent-refined coal processes (SRC-I and SRC-II) were evaluated for their ability to induce ODC. Single applications of heavy distillate (HD), the SRC-II high-boiling fraction and a potent mouse skin carcinogen, produced ODC induction kinetics which were similar to that for 12-O-tetradecanoylphorbol-13-acetate (TPA). Both HD and TPA stimulated maximal ODC activity 3–5 h after application, with epidermal ODC levels returning to basal levels within 12 h. The magnitude of ODC induction after multiple applications of HD was not as great as that observed for TPA. Single skin applications of TPA and HD also transiently elevated hepatic ODC levels 27- and 7-fold, respectively; however, liver ODC activity did not increase following multiple applications of either chemical. Further, ODC induction by HD was also dose-dependent. Relative to controls, single applications of HD and process solvent (boiling range >250°C) elevated ODC levels 145- to 205-fold, light distillate and light oil (boiling range
ISSN:0143-3334
1460-2180
DOI:10.1093/carcin/4.7.805