Quantitative estimation of the extent of alkylation of DNA following treatment of mammalian cells with non-radioactive alkylating agents
- PMID: 7266573
- DOI: 10.1016/0165-7992(81)90006-3
Quantitative estimation of the extent of alkylation of DNA following treatment of mammalian cells with non-radioactive alkylating agents
Abstract
Alkaline sucrose sedimentation has been used to quantitate phosphotriester formation following treatment of human cells with the monofunctional alkylating agents methyl and ethyl methanesulfonate. These persistent alkaline-labile lesions are not repaired during short-term culture conditions and thus serve as a useful and precise index of the total alkylation of the DNA. Estimates of alkylation by this procedure compare favorably with direct estimates by use of labeled alkylating agents.
Similar articles
-
Commentary. Monofunctional alkylating agents and apurinic sites in DNA.Biochem Pharmacol. 1974 Jan 1;23(1):3-8. doi: 10.1016/0006-2952(74)90307-4. Biochem Pharmacol. 1974. PMID: 4590108 No abstract available.
-
Molecular dosimetry of DNA damage caused by alkylation. I. Single-strand breaks induced by ethylating agents in cultured mammalian cells in relation to survival.Mutat Res. 1982 Feb 22;92(1-2):361-77. doi: 10.1016/0027-5107(82)90236-6. Mutat Res. 1982. PMID: 7201070
-
Fluoride ion catalyzed alkylation of nucleic acid derivatives using trialkyl phosphates, dialkyl sulfates and alkyl methanesulfonates.Nucleic Acids Res. 1979;6(6):2261-73. doi: 10.1093/nar/6.6.2261. Nucleic Acids Res. 1979. PMID: 223127 Free PMC article.
-
International Commission for Protection Against Environmental Mutagens and Carcinogens. The subtlety of alkylating agents in reactions with biological macromolecules.Mutat Res. 1994 Feb 1;305(1):13-32. doi: 10.1016/0027-5107(94)90123-6. Mutat Res. 1994. PMID: 7508544 Review.
-
Distribution of methyl and ethyl adducts following alkylation with monofunctional alkylating agents.Mutat Res. 1990 Jul;231(1):11-30. doi: 10.1016/0027-5107(90)90173-2. Mutat Res. 1990. PMID: 2195323 Review.
Cited by
-
Comprehensive High-Resolution Mass Spectrometric Analysis of DNA Phosphate Adducts Formed by the Tobacco-Specific Lung Carcinogen 4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanone.Chem Res Toxicol. 2015 Nov 16;28(11):2151-9. doi: 10.1021/acs.chemrestox.5b00318. Epub 2015 Oct 12. Chem Res Toxicol. 2015. PMID: 26398225 Free PMC article.
-
Methyl DNA Phosphate Adduct Formation in Rats Treated Chronically with 4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanone and Enantiomers of Its Metabolite 4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanol.Chem Res Toxicol. 2018 Jan 16;31(1):48-57. doi: 10.1021/acs.chemrestox.7b00281. Epub 2017 Nov 30. Chem Res Toxicol. 2018. PMID: 29131934 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources