Analysis of tamoxifen-DNA adducts in endometrial explants by MS and 32P-postlabeling |
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Authors: | Beland Frederick A Churchwell Mona I Hewer Alan Phillips David H da Costa Gonçalo Gamboa Marques M Matilde |
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Affiliation: | Division of Biochemical Toxicology, National Center for Toxicological Research, Jefferson, AR 72079, USA. fbeland@nctr.fda.gov |
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Abstract: | ![]() The nonsteroidal antiestrogen tamoxifen increases the risk of endometrial cancer; however, the mechanism for the induction of these tumors is not known. Recently, Sharma et al. [Biochem. Biophys. Res. Commun. 307 (2003) 157], using high performance liquid chromatography (HPLC) with online postcolumn photochemical activation and fluorescence detection, reported the presence of (E)-alpha-(deoxyguanosin- N2-yl)tamoxifen in DNA from human endometrial explants incubated with tamoxifen. Inasmuch as the methodology used by these investigators does not allow unambiguous characterization of tamoxifen-DNA adducts, we have used two additional techniques (HPLC coupled with electrospray ionization tandem mass spectrometry and 32P-postlabeling analyses) to assay for the presence of tamoxifen-DNA adducts in the human endometrial explant DNA. Tamoxifen-DNA adducts were not detected by either method. |
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Keywords: | Tamoxifen 32P-postlabeling HPLC Electrospray ionization tandem mass spectrometry DNA adducts Endometrial cancer |
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