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[中国女性雌激素代谢基因COMT、CYP17单核苷酸多态性与乳腺癌风险的关系]

[Relation between single nucleotide polymorphism in estrogen-metabolizing genes COMT, CYP17 and breast cancer risk among Chinese women].

作者信息

Tan Wen, Qi Jun, Xing De-Yin, Miao Xiao-Ping, Pan Kai-Feng, Zhang Lian, Lin Dong-Xin

机构信息

Department of Etiology and Carcinogenesis, Cancer Institute (Hospital), Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing 100021, China.

出版信息

Zhonghua Zhong Liu Za Zhi. 2003 Sep;25(5):453-6.

Abstract

OBJECTIVE

To test the hypothesis whether polymorphism in estrogen-metabolizing genes, COMT and CYP17, impacts on the risk of breast cancer among Chinese women.

METHODS

COMT (Val158Met) and CYP17 (T1931C) polymorphisms were detected by PCR-based restriction fragment length polymorphism analysis in 250 breast cancer patients and 250 frequency-matched normal controls. Odds ratios (ORs) and 95% confidence intervals (CIs) were estimated by unconditional logistic regression.

RESULTS

COMT Met/Met genotype was found in 10.4% of breast cancer patients, which was significantly higher (P = 0.03) than that in controls (5.2%). Women with Met/Met genotype showed 2-fold increased risk for breast cancer (adjusted OR 2.1, 95% CI 1.1 - 4.5) compared with those with Val/Val or Val/Met genotypes. Stratified analysis showed that the elevated risk of breast cancer, associating with the COMT Met/Met genotype, was evident only among premenopausal women (adjusted OR 4.1, 95% CI 1.2 - 17.3) but not among postmenopausal women (adjusted OR 1.3, 95% CI 0.5 - 3.5). There was no significant difference in the distribution of CYP17 genotypes between breast cancer patients and the control subjects (P = 0.83).

CONCLUSION

The allele encoding for low activity COMT, but not CYP17, may be a genetic risk factor for breast cancer among Chinese women.

摘要

目的

检验雌激素代谢基因COMT和CYP17的多态性是否影响中国女性患乳腺癌的风险这一假设。

方法

采用基于聚合酶链反应的限制性片段长度多态性分析方法,检测250例乳腺癌患者和250例频率匹配的正常对照者的COMT(Val158Met)和CYP17(T1931C)多态性。通过非条件逻辑回归估计比值比(OR)和95%置信区间(CI)。

结果

在10.4%的乳腺癌患者中发现了COMT Met/Met基因型,显著高于对照组(5.2%)(P = 0.03)。与携带Val/Val或Val/Met基因型的女性相比,携带Met/Met基因型的女性患乳腺癌的风险增加了2倍(调整后的OR为2.1,95%CI为1.1 - 4.5)。分层分析显示,与COMT Met/Met基因型相关的乳腺癌风险升高仅在绝经前女性中明显(调整后的OR为4.1,95%CI为1.2 - 17.3),而在绝经后女性中不明显(调整后的OR为1.3,95%CI为0.5 - 3.5)。乳腺癌患者和对照者之间CYP17基因型的分布没有显著差异(P = 0.83)。

结论

编码低活性COMT的等位基因而非CYP17,可能是中国女性患乳腺癌的一个遗传风险因素。

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