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    Bracken (Pteridium aquilinum)-induced DNA adducts in mouse tissues are different from the adduct induced by the activated form of the Bracken carcinogen ptaquiloside.

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    Authors
    Freitas, R N
    O'Connor, Peter J
    Prakash, A S
    Shahin, M
    Povey, Andrew C
    Affiliation
    Cancer Research Campaign Carcinogenesis Group, Paterson Institute for Cancer Research, Manchester M20 9BX, United Kingdom.
    Issue Date
    2001-02-23
    
    Metadata
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    Abstract
    Following treatment with bracken fern (Pteridium aquilinum) extract and bracken spores a number of DNA adducts were detected by (32)P-postlabeling. Three of these adducts have been described previously (Povey et al., Br. J. Cancer (1996) 74, 1342-1348) and in this study, using a slightly different protocol, four new adducts, with higher chromatographic mobility, were detected at levels ranging from 50 to 230% of those previously described. When DNA was treated in vitro with activated ptaquiloside (APT) and analysed by butanol extraction or nuclease P1 treatment, only one adduct was detected by (32)P-postlabeling. This adduct was not present in the DNA from mice treated with bracken fern or spores, suggesting either that bracken contains genotoxins other than ptaquiloside or that the metabolism of ptaquiloside produces genotoxins not reflected by activated ptaquiloside. However, as the ATP-derived adduct has been detected previously in ileal DNA of bracken-fed calves, species-specific differences in the metabolism of bracken genotoxins may exist, thereby leading to differences in their biological outcomes.
    Citation
    Bracken (Pteridium aquilinum)-induced DNA adducts in mouse tissues are different from the adduct induced by the activated form of the Bracken carcinogen ptaquiloside. 2001, 281 (2):589-94 Biochem. Biophys. Res. Commun.
    Journal
    Biochemical and Biophysical Research Communications
    URI
    http://hdl.handle.net/10541/85602
    DOI
    10.1006/bbrc.2001.4388
    PubMed ID
    11181088
    Type
    Article
    Language
    en
    ISSN
    0006-291X
    ae974a485f413a2113503eed53cd6c53
    10.1006/bbrc.2001.4388
    Scopus Count
    Collections
    All Paterson Institute for Cancer Research

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