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针对FTO基因rs1477196和rs9939609单核苷酸多态性的特异性TaqMan等位基因鉴别分析表明,在伊朗女性中,这些单核苷酸多态性与乳腺癌风险之间不存在关联。

Specific TaqMan allelic discrimination assay for rs1477196 and rs9939609 single nucleotide polymorphisms of FTO gene demonstrated that there is no association between these SNPs and risk of breast cancer in Iranian women.

作者信息

Mojaver Mahboobeh, Mokarian Fariborz, Kazemi Mohammad, Salehi Mansoor

机构信息

Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, and Medical Genetics Center of Genome, Shariati St., Isfahan, Iran.

Department of Clinical Oncology, Medical School, Isfahan University of Medical Sciences, Isfahan, and Medical Genetics Center of Genome, Shariati St., Isfahan, Iran.

出版信息

Adv Biomed Res. 2015 Jul 27;4:136. doi: 10.4103/2277-9175.161532. eCollection 2015.

Abstract

BACKGROUND

Breast cancer (BC), is the most common cancer in women, that is the major cause of cancer-related morbidity and mortality in women. Obesity is considered as a major risk factor for BC that increases both the rate and intensity of the disease. Polymorphisms in FTO gene, a known obesity related gene, is shown to be associated with obesity-related traits as well. The aim of this study was to evaluate the association between previously reported single nucleotide polymorphisms (SNPs) of intron 1of FTO gene, rs1477196 and rs9939609 and risk of BC in a subset of Iranian BC patients.

MATERIALS AND METHODS

We genotyped 99 cases and 100 controls for the two SNPs of rs9939609 and rs1477196 by TaqMan allelic discrimination assay. For each sample in an allelic discrimination assay, a unique pair of fluorescent dye probe is used. One fluorescent dye probe has a perfect match with the wild type allele and the other fluorescent dye probe is perfectly matched to the mutated allele.

RESULTS

Our research has shown that the observed differences between case and control groups in the studied SNPs of FTO gene are not statistically significant (P > 0.05).

CONCLUSIONS

Our findings suggest that there is no association between rs9939609 and rs1477196 polymorphisms in FTO gene and increase in risk of BC in the studied Iranian population. These results were inconsistent with that of previously reported case-control studies with BC that means presence of these polymorphisms depends on ethnic group.

摘要

背景

乳腺癌(BC)是女性中最常见的癌症,是女性癌症相关发病和死亡的主要原因。肥胖被认为是BC的主要危险因素,它会增加该疾病的发病率和严重程度。FTO基因是一种已知的与肥胖相关的基因,其多态性也被证明与肥胖相关特征有关。本研究的目的是评估先前报道的FTO基因内含子1的单核苷酸多态性(SNP)rs1477196和rs9939609与一部分伊朗BC患者患BC风险之间的关联。

材料与方法

我们通过TaqMan等位基因鉴别分析法对99例病例和100例对照进行了rs9939609和rs1477196这两个SNP的基因分型。在等位基因鉴别分析中,对于每个样本,使用一对独特的荧光染料探针。一个荧光染料探针与野生型等位基因完全匹配,另一个荧光染料探针与突变型等位基因完全匹配。

结果

我们的研究表明,在FTO基因研究的SNP中,病例组和对照组之间观察到的差异无统计学意义(P>0.05)。

结论

我们的研究结果表明,在研究的伊朗人群中,FTO基因的rs9939609和rs1477196多态性与BC风险增加之间没有关联。这些结果与先前报道的BC病例对照研究结果不一致,这意味着这些多态性的存在取决于种族群体。

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