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[Cancer Research 48, 5065-5070, September 15, 1988]
© 1988 American Association for Cancer Research

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Antibodies against 7-Methyldeoxyguanosine: Its Detection in Rat Peripheral Blood Lymphocyte DNA and Potential Applications to Molecular Epidemiology1

Paolo Degan2,3,, Ruggero Montesano and Christopher P. Wild3,4,

Unit of Mechanisms of Carcinogenesis, International Agency for Research on Cancer, 150 Cours Albert Thomas, 69372 Lyon Cedex, 08 France

Polyclonal antibodies have been raised against the imidazole ring-open form of 7-methyldeoxyguanosine (7-mdGua). A combined high performance liquid chromatography/immunoassay method has been developed using these antibodies which provides a specific and sensitive way to quantitate 7-mdGua in DNA. Following enzyme hydrolysis and chromatographic purification of 7-mdGua, the adduct is quantitatively converted to the ring-open form and can be measured at levels as low as 0.05 pmol by immunoassay. With 1 mg of DNA a level below 1 adduct per 107 normal deoxynucleosides can be measured. Using DNA modified by radiolabeled carcinogens, a good correlation between 7-mdGua levels, as measured by immunoassay or radioactivity, was obtained. In rats treated with dimethylnitrosamine (0.4 and 1.0 mg/kg), both 7-mdGua and O6-methyldeoxyguanosine were detected in peripheral blood lymphocyte DNA. In addition the levels of both adducts at time points up to 48 h posttreatment were very similar to those seen in liver DNA from the same animals. The measurement of 7-mdGua, quantitatively the major methylation adduct, in small cell samples such as lymphocytes has great potential in determining the exposure of humans to environmental methylating agents such as nitrosamines.

1 This investigation was supported by National Cancer Institute Grant IU01. ES04281-01.

2 Present address: Istituto per lo Studio e la Cura del Cancro, Viale Benedetto XV, 10, 16132 Genoa, Italy.

3 Work carried out during the tenure of an International Agency for Research on Cancer Training Fellowship.

4 To whom requests for reprints should be addressed.

Received 1/31/87. Accepted 6/14/88.




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HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
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Copyright © 1988 by the American Association for Cancer Research.