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结直肠癌中代谢酶与吸烟相互作用的病例对照研究。 (注:原文表述可能有误,推测正确表述应为case-control study,翻译为病例对照研究 ,而不是case-only study病例单一研究 )

Case-only study of interactions between metabolic enzymes and smoking in colorectal cancer.

作者信息

Fan Chunhong, Jin Mingjuan, Chen Kun, Zhang Yongjing, Zhang Shuangshuang, Liu Bing

机构信息

Department of Epidemiology & Health Statistics, School of Public Health, Zhejiang University, Hangzhou, Zhejiang, China.

出版信息

BMC Cancer. 2007 Jun 30;7:115. doi: 10.1186/1471-2407-7-115.

Abstract

BACKGROUND

Gene-gene and gene-environment interactions involved in the metabolism of carcinogens may increase the risk of cancer. Our objective was to measure the interactions between common polymorphisms of P450 (CYP1A2, CYP1B1, CYP2E1), GSTM1 and T1, SULT1A1 and cigarette smoking in colorectal cancer (CRC).

METHODS

A case-only design was conducted in a Chinese population including 207 patients with sporadic CRC. Unconditional logistic regression analysis was performed adjusting for age, gender, alcohol consumption, and cigarette smoking.

RESULTS

The interaction odds ratio (COR) for the gene-gene interaction between CYP1B1 1294G and SULT1A1 638A allele was 2.68 (95% CI: 1.16-6.26). The results of the gene-environment analyses revealed that an interaction existed between cigarette smoking and the CYP1B1 1294G allele for CRC (COR = 2.62, 95%CI: 1.01-6.72), the COR for the interaction of CYP1B1 1294G and smoking history > 35 pack-years was 3.47 (95%CI: 1.12-10.80). No other significant gene-gene and gene-environment interactions were observed.

CONCLUSION

Our results showed that the interaction between polymorphisms in CYP1B1 1294G and SULT1A1*2 may play a significant role on CRC in the Chinese population. Also, it is suggested that the association between cigarette smoking and CRC could be differentiated by the CYP1B1 1294G allele.

摘要

背景

致癌物代谢过程中涉及的基因-基因和基因-环境相互作用可能会增加患癌风险。我们的目标是测量细胞色素P450(CYP1A2、CYP1B1、CYP2E1)、谷胱甘肽S-转移酶M1和T1(GSTM1和T1)、磺基转移酶1A1(SULT1A1)的常见多态性与吸烟在结直肠癌(CRC)中的相互作用。

方法

在中国人群中进行了一项病例对照研究,纳入207例散发性结直肠癌患者。进行无条件逻辑回归分析,并对年龄、性别、饮酒和吸烟进行校正。

结果

CYP1B1 1294G和SULT1A1 638A等位基因之间的基因-基因相互作用的交互比数比(COR)为2.68(95%可信区间:1.16-6.26)。基因-环境分析结果显示,吸烟与CRC的CYP1B1 1294G等位基因之间存在相互作用(COR = 2.62,95%可信区间:1.01-6.72),CYP1B1 1294G与吸烟史>35包年之间的相互作用的COR为3.47(95%可信区间:1.12-10.80)。未观察到其他显著的基因-基因和基因-环境相互作用。

结论

我们的结果表明,CYP1B1 1294G和SULT1A1*2多态性之间的相互作用可能在中国人群的结直肠癌中起重要作用。此外,提示吸烟与结直肠癌之间的关联可通过CYP1B1 1294G等位基因来区分。

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