Urinary 8-hydroxydeoxyguano sine and its analogs as DNA marker of oxidative stress: development of an ELISA and measurement in both bladder and prostate cancers

被引:219
作者
Chiou, CC
Chang, PY
Chan, EC
Wu, TL
Tsao, KC
Wu, JT [1 ]
机构
[1] Univ Utah, Hlth Sci Ctr, Dept Pathol, Salt Lake City, UT 84132 USA
[2] Univ Utah, Hlth Sci Ctr, ARUP, Salt Lake City, UT 84132 USA
[3] Chang Gung Univ, Sch Med Technol, Tao Yuan 333, Taiwan
[4] Chang Gung Mem Hosp, Dept Pathol, Tao Yuan, Taiwan
关键词
8-hydroxyguanine; competitive ELISA; oxidative stress; bladder cancer; prostate cancer;
D O I
10.1016/S0009-8981(03)00191-8
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: 8-hydroxydeoxyguanosine (8-OHdG) is the most frequently detected and studied DNA lesion. Upon DNA repair. 8-OHdG is excreted in the urine. Urinary 8-OHdG is now considered as a biomarker of generalized, cellular oxidative stress and is linked to degenerative diseases including cancer. Methods: We developed a competitive enzyme-linked immunosorbent assay (ELISA) for urinary 8-OHdG by coating BSA conjugated 8-hydroxyguanine (8-OHG) on a microplate. Urine specimens containing 8-OHdG and monoclonal anti-8-OHdG antibody were incubated together in the microwell. Final quantification of bound anti-8-OHdG antibody was estimated by the addition of HRP-conjugated sheep-anti-mouse antibody. Results: The concentration range of the calibration curve was 0-60 ng/ml. The sensitivity of the assay was 0.5 ng/ml. The within-day precision and day-to-day precision were < 10%. The ELISA correlated well with a commercial kit (r=0.9). Our assay measured not only 8-OHdG but also 8-OHG and 8-hyroxyguanine in urine. Increased urinary concentration of 8-OHdG and its analogs were detected in both patients with bladder cancer (70.5 +/- 38.2 ng/mg creatinine) and prostate cancer (58.8 +/- 43.4 ng/mg creatinine) as compared to the healthy control (36.1 +/- 24.5 ng/mg creatinine). Conclusion: Our preliminary data suggest that the competitive ELISA for 8-OHdG and its analogs appears to be a simple method for quantifying the extent of oxidative stress and may have potential for identifying cancer risk. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:87 / 94
页数:8
相关论文
共 19 条
[1]   Urinary 8-oxo-2′-deoxyguanosine -: Source, significance and supplements [J].
Cooke, MS ;
Evans, MD ;
Herbert, KE ;
Lunec, J .
FREE RADICAL RESEARCH, 2000, 32 (05) :381-397
[2]  
Djuric Z, 1996, CANCER, V77, P691, DOI 10.1002/(SICI)1097-0142(19960215)77:4<691::AID-CNCR15>3.3.CO
[3]  
2-L
[4]   Biomarker evidence of DNA oxidation in lung cancer patients: Association of urinary 8-hydroxy-2'-deoxyguanosine excretion with radiotherapy, chemotherapy, and response to treatment [J].
Erhola, M ;
Toyokuni, S ;
Okada, K ;
Tanaka, T ;
Hiai, H ;
Ochi, H ;
Uchida, K ;
Osawa, T ;
Nieminen, MM ;
Alho, H ;
KellokumpuLehtinen, P .
FEBS LETTERS, 1997, 409 (02) :287-291
[5]   The level of typical biomarker of oxidative stress 8-hydroxy-2′-deoxyguanosine is higher in uterine myomas than in control tissues and correlates with the size of the tumor [J].
Foksinski, M ;
Kotzbach, R ;
Szymanski, W ;
Olinski, R .
FREE RADICAL BIOLOGY AND MEDICINE, 2000, 29 (07) :597-601
[6]   8-Oxo-7,8-dihydroguanine and 8-oxo-7,8-dihydro-2′-deoxyguanosine levels in human urine do not depend on diet [J].
Gackowski, D ;
Rozalski, R ;
Roszkowski, K ;
Jawien, A ;
Foksinski, M ;
Olinski, R .
FREE RADICAL RESEARCH, 2001, 35 (06) :825-832
[7]  
Helbock HJ, 1999, METHOD ENZYMOL, V300, P156
[8]   Accumulation of premutagenic DNA lesions in mice defective in removal of oxidative base damage [J].
Klungland, A ;
Rosewell, I ;
Hollenbach, S ;
Larsen, E ;
Daly, G ;
Epe, B ;
Seeberg, E ;
Lindahl, T ;
Barnes, DE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (23) :13300-13305
[9]   Interactions between NO and reactive oxygen species: pathophysiological importance in atherosclerosis, hypertension, diabetes and heart failure [J].
Kojda, G ;
Harrison, D .
CARDIOVASCULAR RESEARCH, 1999, 43 (03) :562-571
[10]   Increased formation of oxidative DNA damage, 8-hydroxy-2′-deoxyguanosine, in human breast cancer tissue and its relationship to GSTP1 and COMT genotypes [J].
Matsui, A ;
Ikeda, T ;
Enomoto, K ;
Hosoda, K ;
Nakashima, H ;
Omae, K ;
Watanabe, M ;
Hibi, T ;
Kitajima, M .
CANCER LETTERS, 2000, 151 (01) :87-95