Dehghan Zahra, Sadeghi Samira, Tabatabaeian Hossein, Ghaedi Kamran, Azadeh Mansoureh, Fazilati Mohammad, Bagheri Fatemeh
Department of Biochemistry, Payame Noor University of Isfahan, Isfahan, Iran.
Division of Genetics, Department of Biology, Faculty of Sciences, University of Isfahan, Isfahan, Iran.
Gene. 2017 May 5;611:9-14. doi: 10.1016/j.gene.2017.02.016. Epub 2017 Feb 23.
Albeit single nucleotide polymorphisms related to ESR1 gene have been studied, only a number of them have been reported to be associated with breast cancer risk. rs1062577 is one of the most recent microRNA-related ESR1 SNPs; however, no study has been conducted to investigate the significance this polymorphism in Iranian population. In this study, we aimed to investigate the frequency and also the association between rs1062577 and breast cancer.
rs1062577 position was genotyped by Tetra-primer ARMS-PCR in totally 182 blood specimens obtained from breast cancer patients (n=86), and healthy blood donors (n=96). The distribution of different genotypes was statistically analyzed in terms of the potential association between rs1062577 different alleles, breast cancer risk and clinicopathological criteria of breast cancer patients.
The statistical analyses confidently indicated that rs1062577 A allele is associated with the increased breast cancer risk in both univariate and multivariate regression models (Odds Ratio=8.403 and 32.602 respectively). rs1062577 T allele was statistically associated with stage I of breast cancer patients (p-value=0.025). In silico studies implied that rs1062577 A allele can alter the binding capacity of ESR1 mRNA and miRNAs via either breakage or formation of hydrogen bonds.
rs1062577 A allele is significantly and dramatically associated with the elevated risk and greater stages of breast cancer.
尽管已经对与ESR1基因相关的单核苷酸多态性进行了研究,但据报道只有其中一些与乳腺癌风险相关。rs1062577是最近发现的与ESR1相关的微小RNA单核苷酸多态性之一;然而,尚未开展研究调查该多态性在伊朗人群中的意义。在本研究中,我们旨在调查rs1062577的频率以及它与乳腺癌之间的关联。
采用四引物扩增受阻突变系统聚合酶链反应(Tetra-primer ARMS-PCR)对从乳腺癌患者(n = 86)和健康献血者(n = 96)获得的总共182份血液样本进行rs1062577位点基因分型。根据rs1062577不同等位基因、乳腺癌风险和乳腺癌患者的临床病理标准之间的潜在关联,对不同基因型的分布进行统计学分析。
统计分析确切表明,在单变量和多变量回归模型中,rs1062577 A等位基因均与乳腺癌风险增加相关(优势比分别为8.403和32.602)。rs1062577 T等位基因与乳腺癌患者的I期在统计学上相关(p值 = 0.025)。电子计算机模拟研究表明,rs1062577 A等位基因可通过氢键的断裂或形成改变ESR1 mRNA与微小RNA的结合能力。
rs1062577 A等位基因与乳腺癌风险升高及更高分期显著且密切相关。