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HERO ID
5153475
Reference Type
Journal Article
Title
UVA light-induced DNA single-strand cleavage by hydroxybenzo[a]pyrenes
Author(s)
Yu, HT; Dong, SM; Fu, PP; Hwang, HM
Year
2002
Is Peer Reviewed?
1
Journal
Polycyclic Aromatic Compounds
ISSN:
1040-6638
EISSN:
1563-5333
Publisher
Taylor and Francis Ltd.
Volume
22
Issue
3-4
Page Numbers
861-870
Language
English
DOI
10.1080/10406630213556
Web of Science Id
WOS:000177949300060
Abstract
UVA light-induced DNA single-strand cleavage by 1-hydroxy, 3-hydroxy, 7-hydroxy, and 9-hydroxybenzo[a]pyrenes (OH-BaPs) and 6-acetoxybenzo[a]pyrene (6-OAc-BaP) was studied. Under experimental conditions, the concentrations of 1-OH, 3-OH, 7-OH, and 9-OH-BaPs and 6-OAc-BaP needed to cause 25% of the supercoiled form I plasmid DNA to become relaxed form II DNA were found to be 0.6, 2.5, 1.0, 1.3, and 1.1 μM, respectively. These concentrations are all smaller than that of BaP, which was 6 μM. These results indicate that on photoirradiation, OH-BaPs are more cytotoxic and/or genotoxic than their parent compound, BaP. Mechanistic studies reveal that singlet oxygen and superoxide free radicals are involved in causing DNA cleavage.
Keywords
benzo[a]pyrene; DNA cleavage; hydroxybenzo[a]pyrenes; light; metabolites; PAH
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