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PDCD6基因的变异与中国人子宫肌瘤风险增加有关。

Variations in the PDCD6 gene are associated with increased uterine leiomyoma risk in the Chinese.

作者信息

Zhang Kui, Zhou Bin, Shi Shaoqing, Song Yaping, Zhang Lin

机构信息

Department of Forensic Biology, West China School of Preclinical and Forensic Medicine, Sichuan University, Chengdu, People's Republic of China.

出版信息

Genet Test Mol Biomarkers. 2013 Jul;17(7):524-8. doi: 10.1089/gtmb.2012.0461. Epub 2013 Apr 3.

Abstract

Programmed cell death 6 (PDCD6) participates in T cell receptor, Fas, and glucocorticoid-induced programmed cell death. To test the relationship between PDCD6 polymorphisms and uterine leiomyomas (UL) risk, we investigated the association of two SNPs (rs4957014 and rs3756712) in PDCD6 with UL risk in a case-control study of 295 unrelated premenopausal UL patients and 436 healthy postmenopausal control subjects in a population of China. Genotypes of the two SNPs were determined with the use of PCR-restriction fragment length polymorphism assay. Significantly increased UL risks were found to be associated with the T allele of rs4957014 and the T allele of rs3756712 (p=0.016, odds ratio [OR]=1.325, 95% confidence intervals [CI]=1.053-1.668 for rs4957014; p<0.0001, OR=1.898, 95% CI=1.457-2.474 for rs3756712, respectively). Increased UL risks were associated with them in different genetic models. The present study provided evidence that rs4957014 and rs3756712 are associated with UL risk, the results indicated that genetic polymorphisms in PDCD6 may contribute to the development of UL.

摘要

程序性细胞死亡6(PDCD6)参与T细胞受体、Fas和糖皮质激素诱导的程序性细胞死亡。为了测试PDCD6基因多态性与子宫肌瘤(UL)风险之间的关系,我们在中国人群中进行了一项病例对照研究,调查了295名无亲缘关系的绝经前UL患者和436名健康绝经后对照者中PDCD6基因的两个单核苷酸多态性(SNP,rs4957014和rs3756712)与UL风险的关联。使用聚合酶链反应-限制性片段长度多态性分析来确定这两个SNP的基因型。发现rs4957014的T等位基因和rs3756712的T等位基因与UL风险显著增加相关(rs4957014:p = 0.016,优势比[OR]=1.325,95%置信区间[CI]=1.053 - 1.668;rs3756712:p < 0.0001,OR = 1.898,95% CI = 1.457 - 2.474)。在不同的遗传模型中,UL风险增加均与它们相关。本研究提供了证据表明rs4957014和rs3756712与UL风险相关,结果表明PDCD6基因的多态性可能有助于UL的发生发展。

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