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诱导型一氧化氮合酶启动子多态性、吸烟与尿路上皮癌风险

Inducible nitric oxide synthase promoter polymorphism, cigarette smoking, and urothelial carcinoma risk.

作者信息

Shen Cheng-Huang, Wang Yuan-Hung, Wang Wen-Chuang, Jou Yeong-Chin, Hsu Hueih-Shing, Hsieh Hsiao-Yen, Chiou Hung-Yi

机构信息

Department of Urology, Chia Yi Christian Hospital, Chia Yi City, Taiwan.

出版信息

Urology. 2007 May;69(5):1001-6. doi: 10.1016/j.urology.2007.02.028.

DOI:10.1016/j.urology.2007.02.028
PMID:17482959
Abstract

OBJECTIVES

Bladder carcinoma has a high inducible nitric oxide synthase (iNOS) content, and a highly polymorphic (CCTTT)n repeat in the iNOS promoter region has been identified. We explored whether this iNOS promoter polymorphism and cigarette smoking are associated with urothelial carcinoma (UC) risk.

METHODS

A total of 250 patients with pathologically confirmed UC and 250 unrelated noncancer controls were serially recruited at the Chia Yi Christian Hospital from August 2002 to May 2005. Multivariate logistic regression analysis was used to calculate the odds ratio and 95% confidence interval (CI).

RESULTS

A significantly increased UC risk was found in those who had smoked more than 30 years (odds ratio 2.4, 95% CI 1.5 to 4.2). The study subjects carrying the 12-repeat allele had a significantly increased UC risk (odds ratio 1.7, 95% CI 1.1 to 2.5). We also found the investigated polymorphism was related to clinical stage (P = 0.043). Of those who had ever smoked, those with the short/long (S/L) and long/long (L/L) genotypes (S, 9 to 11 repeats; L, 12 to 18 repeats) and the 12-repeat allele had a significantly increased UC risk of 3.5 (95% CI 1.7 to 7.3) and 4.5 (95% CI 2.2 to 8.9), respectively. Of the study subjects who had smoked longer than 30 years, those with S/L and L/L genotypes and the 12-repeat allele had significantly increased UC risks of 2.4 (95% CI 1.3 to 4.7) and 3.8 (95% CI 1.8 to 8.0), respectively.

CONCLUSIONS

These findings suggest that the polymorphic (CCTTT)n repeat in the iNOS promoter region might be involved in the development of UC, especially in those who have ever smoked.

摘要

目的

膀胱癌中诱导型一氧化氮合酶(iNOS)含量较高,且已在iNOS启动子区域鉴定出高度多态性的(CCTTT)n重复序列。我们探讨了这种iNOS启动子多态性与吸烟是否与尿路上皮癌(UC)风险相关。

方法

2002年8月至2005年5月期间,在嘉义基督教医院连续招募了250例经病理证实的UC患者和250名无血缘关系的非癌症对照者。采用多因素logistic回归分析计算比值比和95%置信区间(CI)。

结果

发现吸烟超过30年的人群UC风险显著增加(比值比2.4,95%CI 1.5至4.2)。携带12次重复等位基因的研究对象UC风险显著增加(比值比1.7,95%CI 1.1至2.5)。我们还发现所研究的多态性与临床分期有关(P = 0.043)。在曾经吸烟的人群中,短/长(S/L)和长/长(L/L)基因型(S,9至11次重复;L,12至18次重复)以及12次重复等位基因的UC风险分别显著增加3.5倍(95%CI 1.7至7.3)和4.5倍(95%CI 2.2至8.9)。在吸烟超过30年的研究对象中,S/L和L/L基因型以及12次重复等位基因的UC风险分别显著增加2.4倍(95%CI 1.3至4.7)和3.8倍(95%CI 1.8至8.0)。

结论

这些发现表明,iNOS启动子区域的多态性(CCTTT)n重复序列可能参与UC的发生发展,尤其是在曾经吸烟的人群中。

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