Abstract
Originalsprog | Engelsk |
---|---|
Tidsskrift | Cancer Epidemiology, Biomarkers & Prevention |
Vol/bind | 17 |
Udgave nummer | 1 |
Sider (fra-til) | 3-14 |
Antal sider | 11 |
ISSN | 1055-9965 |
DOI | |
Status | Udgivet - 2008 |
Bibliografisk note
Keywords: Cell Death; DNA Damage; DNA Repair; Deoxyguanosine; Diet; Enzyme-Linked Immunosorbent Assay; Humans; Oxidative StressAdgang til dokumentet
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Measurement and meaning of oxidatively modified DNA lesions in urine. / Cooke, Marcus S; Olinski, Ryszard; Loft, Steffen; European Standards Committee on Urinary (DNA) Lesion Analysis.
I: Cancer Epidemiology, Biomarkers & Prevention, Bind 17, Nr. 1, 2008, s. 3-14.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review
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TY - JOUR
T1 - Measurement and meaning of oxidatively modified DNA lesions in urine
AU - Cooke, Marcus S
AU - Olinski, Ryszard
AU - Loft, Steffen
AU - European Standards Committee on Urinary (DNA) Lesion Analysis
N1 - Keywords: Cell Death; DNA Damage; DNA Repair; Deoxyguanosine; Diet; Enzyme-Linked Immunosorbent Assay; Humans; Oxidative Stress
PY - 2008
Y1 - 2008
N2 - BACKGROUND: Oxidatively generated damage to DNA has been implicated in the pathogenesis of a wide variety of diseases. The noninvasive assessment of such damage, i.e., in urine, and application to large-scale human studies are vital to understanding this role and devising intervention strategies. METHODS: We have reviewed the literature to establish the status quo with regard to the methods and meaning of measuring DNA oxidation products in urine. RESULTS: Most of the literature focus upon 8-oxo-7,8-dihydro-2'-deoxyguanosine (8-oxodG), and whereas a large number of these reports concern clinical conditions, there remains (a) lack of consensus between methods, (b) possible contribution from diet and/or cell death, (c) no definitive DNA repair source of urinary 2'-deoxyribonucleoside lesions, and (d) no reference ranges for healthy or diseased individuals. CONCLUSIONS: The origin of 8-oxodG is not identified; however, recent cell culture studies suggest that the action of Nudix hydrolase(s) on oxidative modification of the nucleotide pool is a likely candidate for the 8-oxodG found in urine and, potentially, of other oxidized 2'-deoxyribonucleoside lesions. Literature reports suggest that diet and cell death have minimal, if any, influence upon urinary levels of 8-oxodG and 8-oxo-7,8-dihydroguanine, although this should be assessed on a lesion-by-lesion basis. Broadly speaking, there is consensus between chromatographic techniques; however, ELISA approaches continue to overestimate 8-oxodG levels and is not sufficiently specific for accurate quantification. With increasing numbers of lesions being studied, it is vital that these fundamental issues are addressed. We report the formation of the European Standards Committee on Urinary (DNA) Lesion Analysis whose primary goal is to achieve consensus between methods and establish reference ranges in health and disease.
AB - BACKGROUND: Oxidatively generated damage to DNA has been implicated in the pathogenesis of a wide variety of diseases. The noninvasive assessment of such damage, i.e., in urine, and application to large-scale human studies are vital to understanding this role and devising intervention strategies. METHODS: We have reviewed the literature to establish the status quo with regard to the methods and meaning of measuring DNA oxidation products in urine. RESULTS: Most of the literature focus upon 8-oxo-7,8-dihydro-2'-deoxyguanosine (8-oxodG), and whereas a large number of these reports concern clinical conditions, there remains (a) lack of consensus between methods, (b) possible contribution from diet and/or cell death, (c) no definitive DNA repair source of urinary 2'-deoxyribonucleoside lesions, and (d) no reference ranges for healthy or diseased individuals. CONCLUSIONS: The origin of 8-oxodG is not identified; however, recent cell culture studies suggest that the action of Nudix hydrolase(s) on oxidative modification of the nucleotide pool is a likely candidate for the 8-oxodG found in urine and, potentially, of other oxidized 2'-deoxyribonucleoside lesions. Literature reports suggest that diet and cell death have minimal, if any, influence upon urinary levels of 8-oxodG and 8-oxo-7,8-dihydroguanine, although this should be assessed on a lesion-by-lesion basis. Broadly speaking, there is consensus between chromatographic techniques; however, ELISA approaches continue to overestimate 8-oxodG levels and is not sufficiently specific for accurate quantification. With increasing numbers of lesions being studied, it is vital that these fundamental issues are addressed. We report the formation of the European Standards Committee on Urinary (DNA) Lesion Analysis whose primary goal is to achieve consensus between methods and establish reference ranges in health and disease.
U2 - 10.1158/1055-9965.EPI-07-0751
DO - 10.1158/1055-9965.EPI-07-0751
M3 - Journal article
C2 - 18199707
VL - 17
SP - 3
EP - 14
JO - Cancer Epidemiology, Biomarkers & Prevention
JF - Cancer Epidemiology, Biomarkers & Prevention
SN - 1055-9965
IS - 1
ER -