Masonic Cancer Center, University of Minnesota, Minneapolis, MN 55455, USA.
Carcinogenesis. 2011 Sep;32(9):1366-71. doi: 10.1093/carcin/bgr125. Epub 2011 Jul 6.
N'-Nitrosonornicotine (NNN) and 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) are tobacco-specific nitrosamines. NNN and NNK can induce cancers of the esophagus and lung, respectively, in laboratory animals, but data on human esophageal cancer are lacking. The association between levels of NNN and 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL), an NNK metabolite, in urine samples collected before diagnosis and risk of esophageal cancer was examined in 77 patients with esophageal cancer and 223 individually matched controls, all current smokers, from a cohort of 18244 Chinese men in Shanghai, China, followed from 1986 to 2008. Urinary total NNN (free NNN plus NNN-N-glucuronide) was significantly higher, whereas the percentage of its detoxification product NNN-N-glucuronide was significantly lower in cases than controls. Odds ratios (95% confidence intervals) of esophageal cancer for the second and third tertiles of total NNN were 3.99 (1.25-12.7) and 17.0 (3.99-72.8), respectively, compared with the first tertile after adjustment for urinary total NNAL and total cotinine and smoking intensity and duration (P(trend) < 0.001). The corresponding figures for the percentage of NNN-N-glucuronides were 0.37 (0.17-0.80) and 0.27 (0.11-0.62) (P(trend) = 0.001). Urinary total NNN and the percentage of NNN-N-glucuronides almost completely accounted for the observed association for urinary total NNAL (free NNAL plus its glucuronides), urinary total cotinine and smoking intensity with esophageal cancer risk. These findings along with results of previous studies in laboratory animals support a significant and unique role of NNN in esophageal carcinogenesis in humans.
N'-亚硝基降烟碱(NNN)和 4-(甲基亚硝氨基)-1-(3-吡啶基)-1-丁酮(NNK)是烟草特异性亚硝胺。NNN 和 NNK 分别可诱发动物实验中的食管和肺部肿瘤,但有关人类食管癌的数据尚缺乏。本研究在中国上海的一个 18244 名男性队列中,随访自 1986 年至 2008 年,分析了 77 名食管癌患者和 223 名与之年龄、性别匹配的当前吸烟者在诊断前尿液样本中 NNN 和其代谢产物 4-(甲基亚硝氨基)-1-(3-吡啶基)-1-丁醇(NNAL)的浓度与食管癌风险的关系。病例组尿液中总 NNN(游离 NNN 加 NNN-N-葡萄糖醛酸苷)浓度明显升高,而 NNN-N-葡萄糖醛酸苷的解毒产物比例明显降低。在调整了尿 NNAL 总量、总可替宁和吸烟强度及持续时间后,与第一 tertile 相比,总 NNN 的第二 tertile 和第三 tertile 的食管癌比值比(95%置信区间)分别为 3.99(1.25-12.7)和 17.0(3.99-72.8)(Ptrend < 0.001)。NNN-N-葡萄糖醛酸苷比例的相应数值分别为 0.37(0.17-0.80)和 0.27(0.11-0.62)(Ptrend = 0.001)。尿液中总 NNN 和 NNN-N-葡萄糖醛酸苷的比例几乎完全解释了尿总 NNAL(游离 NNAL 加其葡萄糖醛酸苷)、尿总可替宁和吸烟强度与食管癌风险之间的关系。这些发现以及实验室动物的先前研究结果支持 NNN 在人类食管癌发生中的显著和独特作用。