Dietary polyphenols as topoisomerase II poisons: B ring and C ring substituents determine the mechanism of enzyme-mediated DNA cleavage enhancement

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Dietary polyphenols as topoisomerase II poisons: B ring and C ring substituents determine the mechanism of enzyme-mediated DNA cleavage enhancement is …
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scholarly articleQ13442814

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P356DOI10.1021/TX8000785
P3181OpenCitations bibliographic resource ID987963
P932PMC publication ID2737509
P698PubMed publication ID18461976
P5875ResearchGate publication ID5389639

P50authorNeil OsheroffQ88626020
Omari J. BandeleQ106980819
P2093author name stringSara J Clawson
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Exocyclic DNA lesions stimulate DNA cleavage mediated by human topoisomerase II alpha in vitro and in cultured cells.Q40449702
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Type II DNA topoisomerasesQ41728284
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Biochemical and pharmacological properties of p170 and p180 forms of topoisomerase II.Q42189133
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Benzene metabolites antagonize etoposide-stabilized cleavable complexes of DNA topoisomerase IIalphaQ43684726
Stability, cellular uptake, biotransformation, and efflux of tea polyphenol (-)-epigallocatechin-3-gallate in HT-29 human colon adenocarcinoma cellsQ44260419
1,4-Benzoquinone is a topoisomerase II poisonQ44925131
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Double-stranded DNA cleavage/religation reaction of eukaryotic topoisomerase II: evidence for a nicked DNA intermediateQ45387279
P433issue6
P407language of work or nameEnglishQ1860
P921main subjectpoisoningQ114953
polyphenolQ290439
P304page(s)1253-60
P577publication date2008-06-01
P1433published inChemical Research in ToxicologyQ473530
P1476titleDietary polyphenols as topoisomerase II poisons: B ring and C ring substituents determine the mechanism of enzyme-mediated DNA cleavage enhancement
P478volume21

Reverse relations

cites work (P2860)
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