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鸟氨酸脱羧酶基因多态性与乳腺癌风险。

Genetic polymorphism in ornithine decarboxylase and risk of breast cancer.

机构信息

School of Medicine & Dentistry, College of Life Sciences and Medicine, University of Aberdeen, Medical School, Foresterhill, Aberdeen AB25 2ZD, UK.

出版信息

Fam Cancer. 2009;8(4):307-11. doi: 10.1007/s10689-009-9237-9. Epub 2009 Feb 19.

Abstract

Ornithine decarboxylase (ODC), the first enzyme in the biosynthesis of polyamines, has increased activity in breast cancer tissue compared with benign and normal tissues. The ODC gene contains a single nucleotide polymorphism in which a guanine is substituted for an adenine. This study investigated whether the ODC +316 G > A polymorphism (rs2302615) was associated with the risk of developing breast cancer. A case-control study involving 121 controls, without breast cancer, 46 patients with breast cancer but without a family history, and 130 breast cancer cases with a family history of breast cancer was conducted. A nested PCR-restriction fragment length polymorphism procedure and the TaqMan 5' nuclease assay was used to genotype individuals. Risk was significantly lower for heterozygote (GA genotype) individuals [odds ratio (OR) = 0.39, 95% confidence interval (CI) 0.17-0.86, P = 0.018], or individuals with at least one A allele (OR = 0.44, 95% CI 0.21-0.92, P = 0.027), without family history. This protective effect of having at least one copy of the variant A allele was not as strong, however, in those with a family history of the disease. In sporadic breast cancer, the presence of at least one A allele is protective against the disease. The influence of this polymorphism may be less important in individuals with an inherited breast cancer predisposition.

摘要

鸟氨酸脱羧酶(ODC)是多胺生物合成中的第一个酶,在乳腺癌组织中的活性比良性和正常组织高。ODC 基因中有一个单核苷酸多态性,其中一个鸟嘌呤被腺嘌呤取代。本研究探讨了 ODC+316G>A 多态性(rs2302615)是否与乳腺癌的发病风险有关。进行了一项病例对照研究,共纳入 121 名对照(无乳腺癌)、46 名无家族史的乳腺癌患者和 130 名有乳腺癌家族史的乳腺癌患者。采用巢式 PCR-限制性片段长度多态性和 TaqMan5' 核酸酶检测法对个体进行基因分型。杂合子(GA 基因型)个体的风险显著降低[比值比(OR)=0.39,95%置信区间(CI)0.17-0.86,P=0.018],或至少携带一个 A 等位基因的个体(OR=0.44,95%CI0.21-0.92,P=0.027),无家族史。然而,在有家族史的患者中,至少携带一个变异 A 等位基因的个体的这种保护作用并不那么强烈。在散发性乳腺癌中,至少携带一个 A 等位基因可预防该疾病。该多态性的影响在具有遗传性乳腺癌易感性的个体中可能不太重要。

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