Please use this identifier to cite or link to this item:
Title: Loss of oxidized and chlorinated bases in DNA treated with reactive oxygen species: Implications for assessment of oxidative damage in vivo
Authors: Whiteman, M. 
Hong, H.S.
Jenner, A. 
Halliwell, B. 
Keywords: 5-Chlorocytosine
Hypochlorous acid
Oxidative DNA damage
Issue Date: 2002
Citation: Whiteman, M., Hong, H.S., Jenner, A., Halliwell, B. (2002). Loss of oxidized and chlorinated bases in DNA treated with reactive oxygen species: Implications for assessment of oxidative damage in vivo. Biochemical and Biophysical Research Communications 296 (4) : 883-889. ScholarBank@NUS Repository.
Abstract: Oxidative damage to DNA has been reported to occur in a wide variety of disease states. The most widely used "marker" for oxidative DNA damage is 8-hydroxyguanine. However, the use of only one marker has limitations. Exposure of calf thymus DNA to an ·OH-generating system (CuCl2, ascorbate, H2O2) or to hypochlorous acid (HOCl), led to the extensive production of multiple oxidized or chlorinated DNA base products, as measured by gas chromatography-mass spectrometry. The addition of peroxynitrite (ONOO-) (<200 μM) or SIN-1 (1 mM) to oxidized DNA led to the extensive loss of 8-hydroxyguanine, 5-hydroxycytosine, 2,6-diamino-4-hydroxy-5-formamidopyrimidine, 2-hydroxyadenine, 8-hydroxyadenine, and 4,6-diamino-5-formamidopyrimidine were lost at higher ONOO- concentrations (>200 μM). Exposure of DNA to HOCl led to the generation of 5-Cl uracil and 8-Cl adenine and addition of ONOO- (<200 μM) or SIN-1 (1 mM) led to an extensive loss of 8-Cl adenine and a small loss of 5-Cl uracil at higher concentrations (>500 μM). An ·OH-generating system (CuCl2/ascorbate/H2O2) could also destroy these chlorinated species. Treatment of oxidized or chlorinated DNA with acidified nitrite (NO2-, pH 3) led to substantial loss of various base lesions, in particular 8-OH guanine, 5-OH cytosine, thymine glycol, and 8-Cl adenine. Our data indicate the possibility that when ONOO-, nitrite in regions of low pH or ·OH are produced at sites of inflammation, levels of certain damaged DNA bases could represent an underestimate of ongoing DNA damage. This study emphasizes the need to examine more than one modified DNA base when assessing the role of reactive species in human disease. © 2002 Elsevier Science (USA). All rights reserved.
Source Title: Biochemical and Biophysical Research Communications
ISSN: 0006291X
DOI: 10.1016/S0006-291X(02)02018-1
Appears in Collections:Staff Publications

Show full item record
Files in This Item:
There are no files associated with this item.


checked on Jun 8, 2021


checked on Jun 8, 2021

Page view(s)

checked on Jun 12, 2021

Google ScholarTM



Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.