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    Comet assay studies on the activation of two diaziridinylbenzoquinones in K562 cells.

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    Authors
    Ward, Timothy H
    Butler, John
    Shahbakhti, H
    Richards, J T
    Affiliation
    CRC Department of Cell Culture, Paterson Institute for Cancer Research, Christie Hospital, Manchester, U.K.
    Issue Date
    1997-04-25
    
    Metadata
    Show full item record
    Abstract
    Two versions of the comet assay have been used to identify the difference in the modes of action of AZQ (2,5-diaziridinyl-3,6-bis(carboethoxyamino)-1,4-benzoquinone) and BZQ (2,5-diaziridinyl-3,6-bis(ethanolamino)-1,4-benzoquinone) in human leukaemia K562 cells and a K562-derived resistant cell line, BZQR. Using the standard alkaline assay, AZQ produced dose-dependent changes in the mean comet moments from K562 cells, consistent with the formation of strand breaks. This damage was repaired over a period of 6 hr after removal of the drug. The resistant cell line, BZQR, showed much smaller changes in comet moment under identical conditions. In contrast to AZQ, BZQ did not produce any measurable strand breaks in the K562 or BZQR cells. However, the comet radiation/crosslinking assay and a fluorescence-based assay revealed that BZQ extensively cross-links DNA in K562 cells. The extent of cross-linking is greatly reduced in the resistant cell line.
    Citation
    Comet assay studies on the activation of two diaziridinylbenzoquinones in K562 cells. 1997, 53 (8):1115-21 Biochem. Pharmacol.
    Journal
    Biochemical Pharmacology
    URI
    http://hdl.handle.net/10541/94925
    PubMed ID
    9175716
    Type
    Article
    Language
    en
    ISSN
    0006-2952
    Collections
    All Paterson Institute for Cancer Research

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