Molecular characteristics of catechol estrogen quinones in reactions with deoxyribonucleosides

Douglas E. Stack, Jaeman Byun, Michael L. Gross, Eleanor G. Rogan, Ercole L. Cavalieri

Research output: Contribution to journalArticle

206 Scopus citations

Abstract

Estrogens can have two roles in the induction of cancer: stimulating proliferation of cells by receptor-mediated processes, and generating electrophilic species that can covalently bind to DNA. The latter role is thought to proceed through catechol estrogen metabolites, which can be oxidized to o-quinones that bind to DNA. Four estrogen-deoxyribonucleoside adducts were synthesized by reaction of estrone 3,4-quinone (E1-3,4-Q), 17β-estradiol 3,4-quinone (E2-3,4-Q), or estrone 2,3-quinone (E1-2,3-Q) with deoxyguanosine (dG) or deoxyadenosine (dA) in CH3CO2H/H2O (1:1). Reaction of E1-3,4-Q or E2-3,4-Q with dG produced specifically 7-[4-hydroxyestron-1(α,β,)-yl]guanine (4-OHE1-1(α,β)-N7Gua) or 7-[4-hydroxyestradiol-1(α,β)-yl]guanine (4-OHE2-1(α,β)-N7Gua), respectively, in 40% yield, with loss of deoxyribose. These two quinones did not react with dA, deoxycytidine, or thymidine. When E1-2,3-Q was reacted with dG or dA, N2-(2-hydroxyestron-6-yl)deoxyguanosine (2-OHE1-6-N2dG, 10% yield) and N6-(2-hydroxyestron-6-yl)deoxyadenosine (2-OHE1-6-N6dA, 80% yield), respectively, were formed. These adducts provide insight into the type of DNA damage that can be caused by o-quinones of the catechol estrogens. The estrogen 3,4-quinones are expected to produce depurinating guanine adducts that are lost from DNA, generating apurinic sites, whereas the 2,3-quinones would form stable adducts that remain in DNA, unless repaired. The adducts reported here will be used as references in studies to elucidate the structure of estrogen adducts in biological systems.

Original languageEnglish (US)
Pages (from-to)851-859
Number of pages9
JournalChemical Research in Toxicology
Volume9
Issue number5
DOIs
StatePublished - 1996

ASJC Scopus subject areas

  • Toxicology

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