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首页> 外文期刊>Molecular Biology Reports >Association between the c.*229C>T polymorphism of the topoisomerase IIβ binding protein 1 (TopBP1) gene and breast cancer
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Association between the c.*229C>T polymorphism of the topoisomerase IIβ binding protein 1 (TopBP1) gene and breast cancer

机译:拓扑异构酶IIβ结合蛋白1(TopBP1)基因c。* 229C> T多态性与乳腺癌的关系

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摘要

Topoisomerase IIβ binding protein 1 (TopBP1) is involved in cell survival, DNA replication, DNA damage repair and cell cycle checkpoint control. The biological function of TopBP1 and its close relation with BRCA1 prompted us to investigate whether alterations in the TopBP1 gene can influence the risk of breast cancer. The aim of this study was to examine the association between five polymorphisms (rs185903567, rs116645643, rs115160714, rs116195487, and rs112843513) located in the 3′UTR region of the TopBP1 gene and breast cancer risk as well as allele-specific gene expression. Five hundred thirty-four breast cancer patients and 556 population controls were genotyped for these SNPs. Allele-specific TopBP1 mRNA and protein expressions were determined by using real time PCR and western blotting methods, respectively. Only one SNP (rs115160714) showed an association with breast cancer. Compared to homozygous common allele carriers, heterozygous and homozygous for the T variant had significantly increased risk of breast cancer (adjusted odds ratio=3.81, 95% confidence interval: 1.63–8.34, p=0.001). Mean TopBP1 mRNA and protein expression were higher in the individuals with the CT or TT genotype. There was a significant association between the rs115160714 and tumor grade and stage. Most carriers of minor allele had a high grade (G3) tumors classified as T2-T4N1M0. Our study raises a possibility that a genetic variation of TopBP1 may be implicated in the etiology of breast cancer.
机译:拓扑异构酶IIβ结合蛋白1(TopBP1)参与细胞存活,DNA复制,DNA损伤修复和细胞周期检查点控制。 TopBP1的生物学功能及其与BRCA1的密切关系促使我们研究TopBP1基因的改变是否会影响患乳腺癌的风险。这项研究的目的是检查位于TopBP1基因3'UTR区的五个多态性(rs185903567,rs116645643,rs115160714,rs116195487和rs112843513)与乳腺癌风险以及等位基因特异性基因表达之间的关联。对543名乳腺癌患者和556名人群对照进行了这些SNP的基因分型。等位基因特异性TopBP1 mRNA和蛋白质表达分别通过实时PCR和蛋白质印迹法确定。仅一个SNP(rs115160714)显示与乳腺癌相关。与纯合的普通等位基因携带者相比,T变异的纯合子和纯合子显着增加了患乳腺癌的风险(调整后的优势比= 3.81,95%置信区间:1.63-8.34,p = 0.001)。 CT或TT基因型个体的平均TopBP1 mRNA和蛋白质表达较高。 rs115160714与肿瘤等级和分期之间存在显着关联。大多数次要等位基因携带者患有分类为T2-T4N1M0的高级别(G3)肿瘤。我们的研究提出了TopBP1的遗传变异可能与乳腺癌的病因有关的可能性。

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