Literature DB >> 11511174

Identification and quantification of tamoxifen-DNA adducts in the liver of rats and mice.

A Umemoto1, K Komaki, Y Monden, M Suwa, Y Kanno, M Kitagawa, M Suzuki, C X Lin, Y Ueyama, M A Momen, A Ravindernath, S Shibutani.   

Abstract

A new HPLC gradient system was developed for (32)P-postlabeling analysis to identify and quantify hepatic tamoxifen-DNA adducts of rats and mice treated with tamoxifen. Four stereoisomers of alpha-(N(2)-deoxyguanosinyl)tamoxifen (dG(3')(P)-N(2)-TAM), alpha-(N(2)-deoxyguanosinyl)-N-desmethyltamoxifen (dG(3')(P)-N(2)-N-desmethyl-TAM), and alpha-(N(2)-deoxyguanosinyl)tamoxifen N-oxide (dG(3')(P)-N(2)-TAM N-oxide) were prepared by reacting either alpha-acetoxytamoxifen, alpha-acetoxy-N-desmethyltamoxifen or alpha-acetoxytamoxifen N-oxide with 2'-deoxyguanosine 3'-monophosphate, and used as standard markers for (32)P-postlabeling/HPLC analysis. Our HPLC gradient system can separate the above 12 nucleotide isomers as nine peaks; six peaks representing two each trans epimers (fr-1 and fr-2) of dG(3')(P)-N(2)-TAM, dG(3')(P)-N(2)-N-desmethyl-TAM and dG(3')(P)-N(2)-TAM N-oxide, and three peaks representing a mixture of two cis epimers (fr-3 and fr-4) of nucleotides. Tamoxifen was given to female F344 rats and DBA/2 mice by gavage at doses of 45 mg/kg/day and 120 mg/kg/day, respectively, for 7 days. Totally 15 and 17 tamoxifen-DNA adducts were detected in rats and mice, respectively; among them 13 adducts were observed in both rats and mice. trans-dG-N(2)-TAM (fr-2) and trans-dG(3')(P)-N(2)-N-desmethyl-TAM (fr-2) were two major adducts in both animals. Except for these two adducts, trans-dG-N(2)-TAM N-oxide (fr-2) was the third abundant adduct that accounted for 6.4% of the total adducts in mice, while this accounted for only 0.3% in rats. A trans-isomer (fr-1) and cis-isomers (fr-3 and -4) of dG(3')(P)-N(2)-TAM, dG(3')(P)-N(2)-N-desmethyl-TAM and dG(3')(P)-N(2)-TAM N-oxide were also detected as minor adducts in both animals except for cis-form of dG-N(2)-TAM N-oxide in rats. Although the administered dose for rats was 2.7-fold less than that for mice, the total adduct level of rats (216 adducts/10(8) nucleotides) were 3.8-fold higher than mice (56.2 adducts/10(8) nucleotides). Thus, these three types of tamoxifen adducts accounted for 95.0 and 92.5% of the total DNA adducts of the rats and mice, respectively. The formation of tamoxifen adducts primarily resulted from alpha-hydroxylation of tamoxifen.

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Year:  2001        PMID: 11511174     DOI: 10.1021/tx010012d

Source DB:  PubMed          Journal:  Chem Res Toxicol        ISSN: 0893-228X            Impact factor:   3.739


  10 in total

1.  Peroxidase-mediated dealkylation of tamoxifen, detected by electrospray ionization-mass spectrometry, and activation to form DNA adducts.

Authors:  Nilesh W Gaikwad; William J Bodell
Journal:  Free Radic Biol Med       Date:  2011-10-18       Impact factor: 7.376

Review 2.  Biochemical applications of ultrathin films of enzymes, polyions and DNA.

Authors:  James F Rusling; Eli G Hvastkovs; Dominic O Hull; John B Schenkman
Journal:  Chem Commun (Camb)       Date:  2007-08-30       Impact factor: 6.222

3.  Electrochemiluminescent Arrays For Toxicity Screening.

Authors:  James F Rusling
Journal:  Electrochem Soc Interface       Date:  2009

4.  Antiestrogens and the formation of DNA damage in rats: a comparison.

Authors:  Sung Yeon Kim; Naomi Suzuki; Y R Santosh Laxmi; Atsushi Umemoto; Tomonari Matsuda; Shinya Shibutani
Journal:  Chem Res Toxicol       Date:  2006-06       Impact factor: 3.739

5.  Potential beneficial metabolic interactions between tamoxifen and isoflavones via cytochrome P450-mediated pathways in female rat liver microsomes.

Authors:  Jun Chen; Steven C Halls; Joshua F Alfaro; Zhaohui Zhou; Ming Hu
Journal:  Pharm Res       Date:  2004-11       Impact factor: 4.200

6.  Translesion synthesis past tamoxifen-derived DNA adducts by human DNA polymerases eta and kappa.

Authors:  Manabu Yasui; Naomi Suzuki; Y R Santosh Laxmi; Shinya Shibutani
Journal:  Biochemistry       Date:  2006-10-03       Impact factor: 3.162

Review 7.  Metabolic toxicity screening using electrochemiluminescence arrays coupled with enzyme-DNA biocolloid reactors and liquid chromatography-mass spectrometry.

Authors:  Eli G Hvastkovs; John B Schenkman; James F Rusling
Journal:  Annu Rev Anal Chem (Palo Alto Calif)       Date:  2012-04-05       Impact factor: 10.745

8.  State-of-the-Art Metabolic Toxicity Screening and Pathway Evaluation.

Authors:  Eli G Hvastkovs; James F Rusling
Journal:  Anal Chem       Date:  2016-04-14       Impact factor: 6.986

9.  Differences in metabolite-mediated toxicity of tamoxifen in rodents versus humans elucidated with DNA/microsome electro-optical arrays and nanoreactors.

Authors:  Linlin Zhao; Sadagopan Krishnan; Yun Zhang; John B Schenkman; James F Rusling
Journal:  Chem Res Toxicol       Date:  2009-02       Impact factor: 3.739

Review 10.  Screening Genotoxicity Chemistry with Microfluidic Electrochemiluminescent Arrays.

Authors:  Itti Bist; Kiran Bano; James F Rusling
Journal:  Sensors (Basel)       Date:  2017-05-03       Impact factor: 3.576

  10 in total

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