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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1997-8-28
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pubmed:abstractText |
Photobiological activities of the benzo-spaced psoralen analog furonaphthopyranone 3 have been investigated in cell-free and cellular DNA. The molecular geometry parameters of 3 suggest that it should not form interstrand crosslinks with DNA. With cell-free DNA no evidence for crosslinking but also not for monoadduct formation was obtained; rather, the unnatural furocoumarin 3 induces oxidative DNA modifications under near-UVA irradiation. The enzymatic assay of the photosensitized damage in cell-free PM2 DNA revealed the significant formation of lesions sensitive to formamidopyrimidine DNA glycosylase (Fpg protein). In the photooxidation of calf thymus DNA by the furonaphthopyranone 3, 0.29 +/- 0.02% 8-oxo-7,8-dihydroguanine (8-oxoGua) was observed. With 2'-deoxyguanosine (dGuo), the guanidine-releasing photooxidation products oxazolone and oxoimidazolidine were formed predominately, while 8-oxodGuo and 4-HO-8-oxodGuo were obtained in minor amounts. The lack of a significant D2O effect in the photooxidation of DNA and dGuo reveals that singlet oxygen (type II process) plays a minor role; control experiments with tert-butanol and mannitol confirm the absence of hydroxyl radicals as oxidizing species. The furonaphthopyranone 3 (Ered = -1.93 +/- 0.03V) should act in its singlet-excited state as electron acceptor for the photooxidation of dGuo (delta GET ca -6 kcal/mol), which corroborates photoinduced electron transfer (type I) as a major DNA-oxidizing mechanism. A comet assay in Chinese hamster ovary (CHO) AS52 cells demonstrated that the psoralen analog 3 damages cellular DNA upon near-UVA irradiation; however, no photosensitized mutagenicity was observed in CHO AS52 cell cultures.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/DNA,
http://linkedlifedata.com/resource/pubmed/chemical/DNA, Viral,
http://linkedlifedata.com/resource/pubmed/chemical/Deoxyguanosine,
http://linkedlifedata.com/resource/pubmed/chemical/Ficusin,
http://linkedlifedata.com/resource/pubmed/chemical/Methoxsalen,
http://linkedlifedata.com/resource/pubmed/chemical/Photosensitizing Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Psoralens
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0031-8655
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pubmed:author |
pubmed-author:AdamWW,
pubmed-author:BallmaierDD,
pubmed-author:ChewAA,
pubmed-author:EpeBB,
pubmed-author:GasparroF FFF,
pubmed-author:HuttererRR,
pubmed-author:KaganJJ,
pubmed-author:MöllerMM,
pubmed-author:MielkeKK,
pubmed-author:Saha-MöllerC RCR,
pubmed-author:SchneiderF WFW,
pubmed-author:StopperHH
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pubmed:issnType |
Print
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pubmed:volume |
66
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
46-54
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:9230704-Animals,
pubmed-meshheading:9230704-CHO Cells,
pubmed-meshheading:9230704-Cattle,
pubmed-meshheading:9230704-Cell-Free System,
pubmed-meshheading:9230704-Cricetinae,
pubmed-meshheading:9230704-DNA,
pubmed-meshheading:9230704-DNA, Viral,
pubmed-meshheading:9230704-DNA Damage,
pubmed-meshheading:9230704-Deoxyguanosine,
pubmed-meshheading:9230704-Ficusin,
pubmed-meshheading:9230704-Methoxsalen,
pubmed-meshheading:9230704-Molecular Conformation,
pubmed-meshheading:9230704-Molecular Structure,
pubmed-meshheading:9230704-Mutagenicity Tests,
pubmed-meshheading:9230704-Photochemistry,
pubmed-meshheading:9230704-Photosensitizing Agents,
pubmed-meshheading:9230704-Psoralens,
pubmed-meshheading:9230704-Ultraviolet Rays
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pubmed:year |
1997
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pubmed:articleTitle |
Photochemical and photobiological studies of a furonaphthopyranone as a benzo-spaced psoralen analog in cell-free and cellular DNA.
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pubmed:affiliation |
Institute of Organic Chemistry, University of Würzburg, Germany. adam@chemie.uni-wuerzburg.de
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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