Back to Search Start Over

Human AKR1C Isoforms Oxidize the Potent Proximate Carcinogen 7,12-DMBA-3,4-diol in the Human Lung A549 Carcinoma Cell Line

Authors :
Seon Hwa Lee
Ronald G. Harvey
Ian A. Blair
Nisha T. Palackal
Trevor M. Penning
Source :
Polycyclic Aromatic Compounds. 22:801-810
Publication Year :
2002
Publisher :
Informa UK Limited, 2002.

Abstract

Aldo-keto reductases (AKRs) oxidize structurally diverse PAH trans -dihydrodiols to yield reactive and redox active o -quinones. This study examined the ability of AKR1C2 and AKR1C4 to oxidize PAH trans -dihydrodiols of the benz[ a ]anthracene series. The enzymes oxidized 100% of the racemic trans -dihydrodiols and the highest utilization ratios were observed for the more potent proximate carcinogens 7,12-dimethylbenz[ a ]anthracene-3,4-diol (DMBA-3,4-diol) and 7-methylbenz[ a ]anthracene-3,4-diol (7-MBA-3,4-diol). Human multiple tissue expression array analysis revealed high expression of AKR1C isoforms in the human lung carcinoma cell line A549. Both Western blot analysis using AKR1C9 antisera and enzymatic assays using 1-acenapthanol as substrate confirmed the presence of active AKR1C enzymes in A549 cells. To determine the importance of AKR1C-mediated trans -dihydrodiol oxidation in A549 cells, DMBA-3,4-diol was incubated with cell lysates in the presence of 2-mercaptoethanol. Liquid chromatography/ma...

Details

ISSN :
15635333 and 10406638
Volume :
22
Database :
OpenAIRE
Journal :
Polycyclic Aromatic Compounds
Accession number :
edsair.doi...........f9f4ec061b179be847585c37e62e6cac
Full Text :
https://doi.org/10.1080/10406630290103951