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硒蛋白15千道尔顿(Sep15)基因3'非翻译区的811 C/T多态性与白种女性乳腺癌的关系

The 811 C/T polymorphism in the 3' untranslated region of the selenoprotein 15-kDa (Sep15) gene and breast cancer in Caucasian women.

作者信息

Watrowski Rafał, Castillo-Tong Dan Cacsire, Fabjani Gerhild, Schuster Eva, Fischer Michael, Zeillinger Robert

机构信息

Department of Gynecology and Obstetrics, St. Josefskrankenhaus, Teaching Hospital of the University of Freiburg, Sautierstr. 1, 79104, Freiburg, Germany.

Department of Obstetrics and Gynecology, Molecular Oncology Group, Medical University of Vienna, Ebene 5Q, Währinger Gürtel 18-20, 5Q, 1090, Vienna, Austria.

出版信息

Tumour Biol. 2016 Jan;37(1):1009-15. doi: 10.1007/s13277-015-3847-7. Epub 2015 Aug 12.

Abstract

The 15-kDa selenoprotein (Sep15) is a selenocysteine-containing oxidoreductase in the endoplasmic reticulum that participates in disulfide-bond formation and protein folding control. The 3'-untranslated region (3'-UTR) contains two exclusively linked, polymorphic sites at positions 811 (C/T) and 1125 (G/A), which result in two functional haplotypes: 811C/1125G or 811T/1125A. The 811T/1125A variant occurs significantly more often in African-Americans as compared to Caucasians and has been linked to increased breast cancer risk in black women. We studied the 811C/T (rs5845) Sep15 gene polymorphism in 182 Caucasian women-83 breast cancer cases and 99 healthy controls-by pyrosequencing and polymerase chain reaction. Associations between allelic variants and clinico-pathological variables (e.g., age, stage of disease, tumor type, grading, and receptor status) were investigated. The genotype distribution in breast cancer patients (CC 63.9 %, CT 33.7 %, TT 2.4 %) and controls (69.7 %, CT 28.3 %, TT 2 %) showed no significant difference (OR 0.77, 95 % CI 0.41-1.42, p = 0.4). The overall low prevalence of the T allele was in accordance with that reported for Caucasians in previous studies. There was no significant association between 811C/T Sep15 polymorphism and any of clinico-pathological parameters. In conclusion, we are the first to report on 811C/T SEP 15 polymorphism in white breast cancer patients. Genotype variation within the 3'-UTR of the SEP 15 gene showed no association with breast cancer risk or clinico-pathological parameters in Caucasian women.

摘要

15千道尔顿硒蛋白(Sep15)是一种在内质网中含硒代半胱氨酸的氧化还原酶,参与二硫键形成和蛋白质折叠调控。3'-非翻译区(3'-UTR)在811位(C/T)和1125位(G/A)含有两个紧密连锁的多态性位点,产生两种功能性单倍型:811C/1125G或811T/1125A。与白种人相比,811T/1125A变异在非裔美国人中出现的频率显著更高,并且与黑人女性患乳腺癌风险增加有关。我们通过焦磷酸测序和聚合酶链反应研究了182名白种女性(83例乳腺癌患者和99名健康对照)中811C/T(rs5845)Sep15基因多态性。研究了等位基因变异与临床病理变量(如年龄、疾病分期、肿瘤类型、分级和受体状态)之间的关联。乳腺癌患者(CC 63.9%,CT 33.7%,TT 2.4%)和对照(CC 69.7%,CT 28.3%,TT 2%)的基因型分布无显著差异(比值比0.77,95%置信区间0.41 - 1.42,p = 0.4)。T等位基因总体低频率与先前研究报道的白种人情况一致。811C/T Sep15多态性与任何临床病理参数之间均无显著关联。总之,我们首次报道了白种乳腺癌患者中SEP 15基因811C/T多态性。SEP 15基因3'-UTR内的基因型变异与白种女性患乳腺癌风险或临床病理参数无关。

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