Detection of estrogen DNA-adducts in human breast tumor tissue and healthy tissue by combined nano LC-nano ES tandem mass spectrometry
- 1 May 2003
- journal article
- Published by American Chemical Society (ACS) in Journal of the American Society for Mass Spectrometry
- Vol. 14 (5) , 482-491
- https://doi.org/10.1016/s1044-0305(03)00130-2
Abstract
For the first time estrogen DNA-adducts were identified in DNA human breast tumor tissue using nano-LC coupled to nano-Electrospray Tandem Mass Spectrometry. Normal breast tissue was analyzed analogously. The data obtained in the five breast tumor and five adjacent normal tissue samples were compared qualitatively, but no straightforward difference was observed. Prior to LC-MS analysis the DNA was enzymatically hydrolyzed to a nucleoside pool. The DNA-hydrolysates were directly injected onto a column switching system developed for on-line sample clean-up and subsequent analysis of the DNA-adducts. In four patients using Premarin, DNA-adducts of 4-hydroxy-equilenin (4OHEN) were detected. All except three samples contained DNA-adducts from 4-hydroxy-estradiol or 4-hydroxy-estrone. Also DNA isolated from eight alcohol fixed and paraffin embedded breast tumor tissue showed the presence of different estrogen DNA-adducts. Worthwhile mentioning is the presence of adducts responding to m/z 570 > m/z 454 transition. This is a well-known SRM-transition indicative for the presence of the 2′-deoxyguanosine (dGuo) adduct of Benzo[a]pyrene.Keywords
This publication has 49 references indexed in Scilit:
- Quantification of 2‘-Fluoro-2‘-deoxyuridine and 2‘-Fluoro-2‘-deoxycytidine in DNA and RNA Isolated from Rats and Woodchucks Using LC/MS/MSChemical Research in Toxicology, 2002
- Characterization of a major aromatic DNA adduct detected in human breast tissuesEnvironmental and Molecular Mutagenesis, 2002
- Measurement of Oxidative DNA Damage by Catechol Estrogens and Analogues in VitroChemical Research in Toxicology, 1999
- The Major Metabolite of Equilin, 4-Hydroxyequilin, Autoxidizes to an o-Quinone Which Isomerizes to the Potent Cytotoxin 4-Hydroxyequilenin-o-quinoneChemical Research in Toxicology, 1999
- Alkylation of 2‘-Deoxynucleosides and DNA by the Premarin Metabolite 4-Hydroxyequilenin Semiquinone RadicalChemical Research in Toxicology, 1998
- Functional role of estrogen metabolism in target cells: review and perspectivesCarcinogenesis: Integrative Cancer Research, 1998
- Reaction of the Premarin Metabolite 4-Hydroxyequilenin Semiquinone Radical with 2‘-Deoxyguanosine: Formation of Unusual Cyclic AdductsJournal of the American Chemical Society, 1997
- Estrogen−Nucleic Acid Adducts: Reaction of 3,4-Estrone o-Quinone with Nucleic Acid BasesChemical Research in Toxicology, 1997
- Characterization of an N6-oxopropenyl-′-deoxyadenosine adduct in malondialdehyde-modified DNA using liquid chromatography/electrospry ionization tandem mass spectrometryCarcinogenesis: Integrative Cancer Research, 1996
- Hormonal carcinogenesis: Separation of estrogenicity from carcinogenicityChemico-Biological Interactions, 1986