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N-乙酰转移酶2的基因多态性与结直肠癌风险

Genetic polymorphisms of N-acetyltransferase 2 and colorectal cancer risk.

作者信息

He Lu-Jun, Yu Yue-Ming, Qiao Fang, Liu Jing-Shan, Sun Xiao-Feng, Jiang Ling-Ling

机构信息

Department of Biochemistry, Hebei Medical University, Shijiazhuang 050017, Hebei Province, China.

出版信息

World J Gastroenterol. 2005 Jul 21;11(27):4268-71. doi: 10.3748/wjg.v11.i27.4268.

Abstract

AIM

To identify the distribution of N-acetyltrasferase 2(NAT2) polymorphism in Hebei Han Chinese and the effects of the polymorphism on the development of colorectal cancer.

METHODS

We performed a hospital-based case-control study of 237 healthy individuals and 83 colorectal cancer patients of Hebei Han Chinese. DNA was extracted from peripheral blood and cancer tissues. The genotypes of the polymorphisms were assessed by PCR-restriction fragment length polymorphism (RFLP).

RESULTS

There were four NAT2 alleles of WT, M1, M2, and M3 both in the healthy subjects and in the patients, and 10 genotypes of WT/WT, WT/M1, WT/M2, WT/M3, M1/M1, M1/M2, M1/M3, M2/M2, M2/M3, M3/M3. M2 allele was present in 15.61% of healthy subjects and 29.52% of patients (chi(2) = 15.31, P<0.0001), and M3 allele was present in 30.59% of healthy subjects and 16.87% of patients (chi(2) = 25.33, P<0.0001). There were more WT/M2 (chi(2) = 34.42, P<0.0001, odd ratio = 4.99, 95%CI = 2.27-9.38) and less WT/M3 (chi(2) = 3.80, P = 0.03) in the patients than in the healthy subjects. In 70.3% of the patients, there was a difference in NAT2 genotype between their tumors and blood cells. Patients had more WT/M2 (chi(2) = 5.11, P = 0.02) and less M2/M3 (chi(2) = 4.27, P = 0.039) in their blood cells than in the tumors. Furthermore, 53.8% (7/13) of M2/M3 in tumors were from WT/M2 of blood cells.

CONCLUSION

There is a possible relationship between the NAT2 polymorphisms and colorectal cancer in Hebei Han Chinese. The genotype WT/M2 may be a risk factor for colorectal cancer.

摘要

目的

确定河北汉族人群中N - 乙酰转移酶2(NAT2)基因多态性的分布及其对结直肠癌发生发展的影响。

方法

我们对237名河北汉族健康个体和83名结直肠癌患者进行了一项基于医院的病例对照研究。从外周血和癌组织中提取DNA。通过聚合酶链反应 - 限制性片段长度多态性(PCR - RFLP)评估多态性的基因型。

结果

健康受试者和患者中均存在WT、M1、M2和M3这四种NAT2等位基因,以及WT/WT、WT/M1、WT/M2、WT/M3、M1/M1、M1/M2、M1/M3、M2/M2、M2/M3、M3/M3这10种基因型。M2等位基因在15.61%的健康受试者和29.52%的患者中存在(χ² = 15.31,P < 0.0001),M3等位基因在30.59%的健康受试者和16.87%的患者中存在(χ² = 25.33,P < 0.0001)。患者中WT/M2基因型比健康受试者更多(χ² = 34.42,P < 0.0001,比值比 = 4.99,95%可信区间 = 2.27 - 9.38),而WT/M3基因型比健康受试者更少(χ² = 3.80,P = 0.03)。在70.3%的患者中,肿瘤组织和血细胞之间的NAT2基因型存在差异。患者血细胞中的WT/M2基因型比肿瘤组织更多(χ² = 5.11,P = 0.02),而M2/M3基因型比肿瘤组织更少(χ² = 4.27,P = 0.039)。此外,肿瘤组织中53.8%(7/13)的M2/M3基因型来自血细胞中的WT/M2基因型。

结论

河北汉族人群中NAT2基因多态性与结直肠癌之间可能存在关联。WT/M2基因型可能是结直肠癌的一个危险因素。

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