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Analysis of tamoxifen-DNA adducts in endometrial explants by MS and 32P-postlabeling
Authors:Beland Frederick A  Churchwell Mona I  Hewer Alan  Phillips David H  da Costa Gonçalo Gamboa  Marques M Matilde
Affiliation:Division of Biochemical Toxicology, National Center for Toxicological Research, Jefferson, AR 72079, USA. fbeland@nctr.fda.gov
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.
Keywords:Tamoxifen   32P-postlabeling   HPLC   Electrospray ionization tandem mass spectrometry   DNA adducts   Endometrial cancer
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