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胰岛素样生长因子结合蛋白3(IGFBP3)基因的遗传多态性:与中国女性乳腺癌风险及血液中IGFBP-3蛋白水平的关联

Genetic polymorphisms in the IGFBP3 gene: association with breast cancer risk and blood IGFBP-3 protein levels among Chinese women.

作者信息

Ren Zefang, Cai Qiuyin, Shu Xiao-Ou, Cai Hui, Li Chun, Yu Herbert, Gao Yu-Tang, Zheng Wei

机构信息

Department of Medicine, Vanderbilt University, Nashville, TN, USA.

出版信息

Cancer Epidemiol Biomarkers Prev. 2004 Aug;13(8):1290-5.

Abstract

Cumulative evidence suggests that insulin-like growth factors (IGF) play an important role in the etiology of breast cancer. The IGF binding proteins regulate the action of IGFs, and >90% of circulating IGFs are bound to IGFBP-3. We evaluated the associations of five (A-202C, G227C, C3804G, 5606InsA, and C5827T) genetic polymorphisms in the IGFBP3 gene with breast cancer risk and the blood IGFBP-3 protein level in a population-based, case-control study conducted among Chinese women in Shanghai. Genomic DNA samples from 1,193 incident breast cancer patients and 1,310 community controls were genotyped for IGFBP3 polymorphisms. Blood IGFBP-3 levels were determined for 390 controls. A 30% to 60% elevated risk of breast cancer was found to be associated with homozygosity for the variant allele in polymorphisms A-202C, G227C, 5606InsA, and C5827T. Carrying the variant allele in C3804G was also associated with an increased risk. About 13.5% of cases and 9.7% of controls had one or more of the above risk genotypes, resulting in odds ratio [OR; 95% confidence interval (95% CI)] of 1.4 (1.0-1.9). The ORs (95% CIs) were 1.3 (1.0-1.8) and 1.7 (1.1-2.5) for women with one to two and three to five risk genotypes, respectively (P for trend < 0.01). Four common haplotypes for the IGFBP3 gene were identified. Compared with the haplotype containing only the wild-type allele in the five loci, the haplotype with the variant allele in all sites was associated with an elevated risk of breast cancer (OR 1.4, 95% CI 1.0-1.9), particularly among younger women (OR 2.3, 95% CI 1.3-3.9). With the exception of C3804G, in which no homozygote was identified, the level of circulating IGFBP-3 was reduced in a dose-response manner with an increasing number of variant alleles in each of the other four polymorphic sites (P for trend < 0.05). These results indicated that IGFBP3 polymorphisms may be associated with the level of blood IGFBP-3 protein and an increased risk of breast cancer.

摘要

越来越多的证据表明,胰岛素样生长因子(IGF)在乳腺癌的病因学中起着重要作用。IGF结合蛋白调节IGF的作用,并且超过90%的循环IGF与IGFBP-3结合。在一项以上海中国女性为对象的基于人群的病例对照研究中,我们评估了IGFBP3基因中的五个(A-202C、G227C、C3804G、5606InsA和C5827T)基因多态性与乳腺癌风险以及血液IGFBP-3蛋白水平之间的关联。对1193例新发乳腺癌患者和1310例社区对照的基因组DNA样本进行IGFBP3多态性基因分型。测定了390例对照的血液IGFBP-3水平。发现A-202C、G227C、5606InsA和C5827T多态性中变异等位基因的纯合性与乳腺癌风险升高30%至60%相关。携带C3804G中的变异等位基因也与风险增加相关。约13.5%的病例和9.7%的对照具有一种或多种上述风险基因型,导致优势比[OR;95%置信区间(95%CI)]为1.4(1.0 - 1.9)。具有一至两个和三至五个风险基因型的女性的OR(95%CI)分别为1.3(1.0 - 1.8)和1.7(1.1 - 2.5)(趋势P<0.01)。鉴定出IGFBP3基因的四种常见单倍型。与在五个位点仅包含野生型等位基因的单倍型相比,在所有位点都具有变异等位基因的单倍型与乳腺癌风险升高相关(OR 1.4,95%CI 1.0 - 1.9),特别是在年轻女性中(OR 2.3,95%CI 1.3 - 3.9)。除了未鉴定出纯合子的C3804G外,在其他四个多态性位点中的每一个位点,循环IGFBP-3水平随着变异等位基因数量的增加呈剂量反应性降低(趋势P<0.05)。这些结果表明,IGFBP3多态性可能与血液IGFBP-3蛋白水平以及乳腺癌风险增加相关。

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