Li YanLi, Sun Jianya, Shang Huizhen
The occupational health department of TISCO CDC, TaiYuan, 030003, China.
Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi. 2014 Aug;32(8):578-81.
To study the excision repair capacity of human 8-oxoguanine DNA N-glycosylase 1 (hOGG1) for 8-OH-dG and the oxidative DNA damage among workers exposed to nickel in stainless steel production environment.
A total of 231 workers exposed to nickel in a stainless steel production enterprise were recruited as nickel exposure group, and another 75 water pump workers in that enterprise were recruited as control group. The workplace occupational hazard factors were determined. Double-antigen sandwich ELISA was used to determine urinary 8-OH-dG level; RT-PCR was used to determine hOGG1 mRNA level. Pearson correlation was used to analyze the correlation between urinary 8-OH-dG level and hOGG1 mRNA level.
Level of 8-OH-dG was compared between different types of nickel-exposed workers and control workers; rolling mill workers showed no significant difference from the control group (P > 0.05), while steel making workers and steel slag disposing workers showed significant differences from the control group (P < 0.05). Level of 8-OH-dG was also compared between nickel-exposed workers with different working years and control workers; nickel-exposed workers with 0∼5 and 6∼10 working years showed no significant differences from the control group (P > 0.05), while other exposed workers showed significant differences from the control group (P < 0.05). Different types of nickel-exposed workers all showed significant differences from the control group in hOGG1 mRNA level (P < 0.05). Nickel-exposed workers with 0∼5 working years showed no significant difference from the control group in hOGG1 mRNA level (P > 0.05), while other exposed workers showed significant differences from the control group (P < 0.05). Pearson correlation analysis showed that urinary 8-OH-dG level was positively correlated with hOGG1 mRNA level (r = 0.993) in different types of nickel-exposed workers, and the correlation was significant at α = 0.01 (P < 0.05); urinary 8-OH-dG level also showed a positive correlation with hOGG1 mRNA level in nickel-exposed workers with different working years (r = 0.968), and the correlation was significant at α = 0.01 (P < 0.05).
Exposure to nickel increases oxidative DNA damage among steel workers, and hOGG1 shows active excision repair capacity for 8-OH-dG.
研究人8-氧代鸟嘌呤DNA糖基化酶1(hOGG1)对8-羟基脱氧鸟苷(8-OH-dG)的切除修复能力以及不锈钢生产环境中镍暴露工人的氧化性DNA损伤情况。
选取某不锈钢生产企业231名镍暴露工人作为镍暴露组,另选取该企业75名水泵工人作为对照组。测定工作场所职业危害因素。采用双抗原夹心ELISA法测定尿8-OH-dG水平;采用RT-PCR法测定hOGG1 mRNA水平。采用Pearson相关分析尿8-OH-dG水平与hOGG1 mRNA水平的相关性。
比较不同类型镍暴露工人与对照组工人的8-OH-dG水平;轧钢厂工人与对照组比较差异无统计学意义(P>0.05),而炼钢工人和钢渣处理工人与对照组比较差异有统计学意义(P<0.05)。比较不同工龄镍暴露工人与对照组工人的8-OH-dG水平;工龄0~5年和6~10年的镍暴露工人与对照组比较差异无统计学意义(P>0.05),而其他暴露工人与对照组比较差异有统计学意义(P<0.05)。不同类型镍暴露工人的hOGG1 mRNA水平与对照组比较差异均有统计学意义(P<0.05)。工龄0~5年的镍暴露工人hOGG1 mRNA水平与对照组比较差异无统计学意义(P>0.05),而其他暴露工人与对照组比较差异有统计学意义(P<0.05)。Pearson相关分析显示,不同类型镍暴露工人尿8-OH-dG水平与hOGG1 mRNA水平呈正相关(r=0.993),在α=0.01水平上相关性显著(P<0.05);不同工龄镍暴露工人尿8-OH-dG水平与hOGG1 mRNA水平也呈正相关(r=0.968),在α=0.01水平上相关性显著(P<0.05)。
镍暴露增加钢铁工人的氧化性DNA损伤,hOGG1对8-OH-dG具有活跃的切除修复能力。