Urinary 8-isoprostane levels and occurrence of lung, colorectal, prostate, breast and overall cancer: Results from a large, population-based cohort study with 14 years of follow-up

被引:27
|
作者
Gao, Xin [1 ,2 ]
Brenner, Hermann [1 ,3 ,4 ,5 ]
Holleczek, Bernd [6 ]
Cuk, Katarina [1 ]
Zhang, Yan [1 ]
Anusruti, Ankita [1 ,2 ]
Xuan, Yang [1 ,2 ]
Xu, Yiwei [7 ]
Schottker, Ben [1 ,2 ,8 ]
机构
[1] German Canc Res Ctr, Div Clin Epidemiol & Ageing Res, Neuenheimer Feld 581, D-69120 Heidelberg, Germany
[2] Heidelberg Univ, Network Aging Res, Heidelberg, Germany
[3] German Canc Res Ctr, Div Prevent Oncol, Heidelberg, Germany
[4] Natl Ctr Tumor Dis NCT, Heidelberg, Germany
[5] German Canc Res Ctr, German Canc Consortium DKTK, Heidelberg, Germany
[6] Saarland Canc Registry, Saarland, Germany
[7] Univ Wisconsin, Dept Surg, Sch Med & Publ Hlth, Madison, WI USA
[8] FOM Univ, Inst Hlth Care & Social Sci, Essen, Germany
关键词
Neoplasms; Oxidative stress; Cohort study; 8-Isoprostane; Lung cancer; Breast cancer; Colorectal cancer; Prostate cancer; OXIDATIVE STRESS; 8-OXO-7,8-DIHYDRO-2'-DEOXYGUANOSINE EXCRETION; RESPIRATORY-DISEASE; RISK; ASSOCIATION; BIOMARKERS; ISOPROSTANES; INFLAMMATION; SMOKING; SERUM;
D O I
10.1016/j.freeradbiomed.2018.05.065
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Urinary 8 isoprostane is an established biomarker for lipid peroxidation. However, the association between its pre-diagnostic levels and cancer incidence has rarely been evaluated. Methods: 8793 older adults from the German ESTHER cohort were followed up for cancer incidence by cancer registry data. A directed acyclic graph was utilized to identify potential confounders. Multivariate Cox regression models were applied to estimate hazard ratios (HRs) and 95% confidence intervals (95% CI). Results: During 14-year follow-up, 1540 incident cancer cases, including 207 lung, 196 colorectal, 218 breast and 245 prostate cancer cases were detected. 8-isoprostane concentrations were positively associated with lung cancer, but not with cancer at the other sites. The HR (95% CI) for the association with lung cancer was 1.61 (1.10, 2.34) for comparison of the top with bottom tertile in total population. The association of 8-isoprostane levels with lung cancer persisted after the adjustment for smoking and other potential confounders and was multiplicative to the effect of smoking. However, 8-isoprostane levels did not improve lung cancer prediction when added to a model containing age, sex and smoking. A protective association of increasing 8-isoprostane levels was observed for prostate cancer incidence but this association was only statistically significant among current smokers. Discussion: Our findings suggest that lipid peroxidation is involved in the development of lung cancer. However, high oxidative stress may be a protective factor for prostate cancer, especially among current smokers.
引用
收藏
页码:20 / 26
页数:7
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