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白细胞介素-1和白细胞介素-6基因多态性与白人女性患乳腺癌的风险

Interleukin-1 and interleukin-6 gene polymorphisms and the risk of breast cancer in caucasian women.

作者信息

Hefler Lukas A, Grimm Christoph, Lantzsch Tilmann, Lampe Dieter, Leodolter Sepp, Koelbl Heinz, Heinze Georg, Reinthaller Alexander, Tong-Cacsire Dan, Tempfer Clemens, Zeillinger Robert

机构信息

Department of Obstetrics and Gynecology, Medical University of Vienna, Austria.

出版信息

Clin Cancer Res. 2005 Aug 15;11(16):5718-21. doi: 10.1158/1078-0432.CCR-05-0001.

Abstract

PURPOSE

Genetic polymorphisms of cytokine-encoding genes are known to predispose to malignant disease. Interleukin (IL)-1 and IL-6 are crucially involved in breast carcinogenesis. Whether polymorphisms of the genes encoding IL-1 (IL1) and IL-6 (IL6) also influence breast cancer risk is unknown.

EXPERIMENTAL DESIGN

In the present case-control study, we ascertained three polymorphisms of the IL1 gene cluster [-889 C/T polymorphism of the IL1alpha gene (IL1A), -511 C/T polymorphism of the IL1beta promoter (IL1B promoter), a polymorphism of IL1beta exon 5 (IL1B exon 5)], an 86-bp repeat in intron 2 of the IL1 receptor antagonist gene (IL1RN), and the -174 G/C polymorphism of the IL6 gene (IL6) in 269 patients with breast cancer and 227 healthy controls using PCR and pyrosequencing.

RESULTS

Polymorphisms within the IL1 gene cluster and the respective haplotypes were not associated with the presence and the phenotype of breast cancer. The IL6 polymorphism was significantly associated with breast cancer. Odds ratios for women with one or two high-risk alleles versus women homozygous for the low-risk allele were 1.5 (95% confidence interval, 1.04-2.3; P = 0.04) and 2.0 (95% confidence interval, 1.1-3.6; P = 0.02), respectively. No association was ascertained between presence of the IL6 polymorphism and various clinicopathologic variables.

CONCLUSIONS

Although polymorphisms within the IL1 gene cluster do not seem to influence breast cancer risk or phenotype, presence of the -174C IL6 allele increases the risk of breast cancer in Caucasian women in a dose-dependent fashion.

摘要

目的

已知细胞因子编码基因的遗传多态性易导致恶性疾病。白细胞介素(IL)-1和IL-6在乳腺癌发生过程中起关键作用。编码IL-1(IL1)和IL-6(IL6)的基因多态性是否也会影响乳腺癌风险尚不清楚。

实验设计

在本病例对照研究中,我们采用聚合酶链反应(PCR)和焦磷酸测序法,在269例乳腺癌患者和227例健康对照中确定了IL1基因簇的三个多态性位点[IL1α基因(IL1A)的-889 C/T多态性、IL1β启动子(IL1B启动子)的-511 C/T多态性、IL1β外显子5(IL1B外显子5)的一个多态性位点]、IL1受体拮抗剂基因(IL1RN)内含子2中的一个86 bp重复序列以及IL6基因(IL6)的-174 G/C多态性。

结果

IL1基因簇内的多态性位点及相应单倍型与乳腺癌的发生及表型无关。IL6多态性与乳腺癌显著相关。携带一个或两个高危等位基因的女性与携带低危等位基因纯合子的女性相比,比值比分别为1.5(95%置信区间,1.04 - 2.3;P = 0.04)和2.0(95%置信区间,1.1 - 3.6;P = 0.02)。未确定IL6多态性位点的存在与各种临床病理变量之间存在关联。

结论

虽然IL1基因簇内的多态性似乎不影响乳腺癌风险或表型,但-174C IL6等位基因的存在以剂量依赖方式增加了白种女性患乳腺癌的风险。

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