期刊
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION
卷 22, 期 10, 页码 1797-1804出版社
AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1055-9965.EPI-13-0485
关键词
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资金
- NIH [CA111922, CA138671]
- MD Anderson Cancer Center Research Trust
- University of Texas MD Anderson Cancer Center institutional support
Background: Mutagen-induced DNA damage as measured in peripheral blood lymphocytes (PBL) has been associated with increased risks of cancers. The formation of gamma-H2AX is an early cellular response to DNA double-strand breaks (DSB). We hypothesize that higher level of radiation-induced gamma-H2AX in PBLs may be associated with an increased risk of esophageal adenocarcinoma. Methods: Laser scanning cytometer-based immunocytochemical method was used to measure baseline and irradiation-induced gamma-H2AX levels in PBLs from 211 patients with esophageal adenocarcinoma and 211 healthy controls. The ratio of induced gamma-H2AX level to baseline level was used to evaluate individual susceptibility to DSBs. Relative risks for esophageal adenocarcinoma associated with gamma-H2AX were assessed by multivariable logistic regression analysis. Results: Radiation-induced gamma-H2AX level and the g-H2AX ratio were significantly higher in cases than in controls. Dichotomized at the median in controls, a significantly increased risk for esophageal adenocarcinoma was observed in association with high gamma-H2AX ratio [OR = 2.94; 95% confidence interval (CI), 1.83-4.72]. Quartile analyses showed significant dose-response associations between higher gamma-H2AX ratio and increased risk of esophageal adenocarcinoma (P-trend, 1.64E-06). In addition, joint effect between gamma-H2AX ratio and smoking was observed: smokers who had high gamma-H2AX ratio exhibited the highest risk of esophageal adenocarcinoma (OR = 5.53; 95% CI, 2.71-11.25) compared with never smokers with low gamma-H2AX ratio. Conclusion: Radiation-induced DNA damage assessed by gamma-H2AX ratio is associated with an increased risk of esophageal adenocarcinoma. Impact: gamma-H2AX assay is a new and robust method to measure DSB damage in PBLs, which can be used to assess mutagen sensitivity and esophageal adenocarcinoma risk. (C) 2013 AACR.
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