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常见的 TERT 基因变异与中国人群宫颈癌风险相关。

Common genetic variants in TERT contribute to risk of cervical cancer in a Chinese population.

机构信息

Nanjing Maternity and Child Health Hospital of Nanjing Medical University, Nanjing, China.

出版信息

Mol Carcinog. 2012 Oct;51 Suppl 1:E118-22. doi: 10.1002/mc.21872. Epub 2012 Jan 6.

DOI:10.1002/mc.21872
PMID:22228261
Abstract

UNLABELLED

Single-nucleotide polymorphisms (SNPs) of TERT rs2736098, rs2736100, and CLPTM1L rs402710 at 5p15.33 are significantly associated with risk of a spectrum of cancers. However, cervical cancer has been rarely evaluated. In this study, we genotyped the three SNPs in a case-control study with 1,033 cervical cancer cases and 1,053 cancer-free controls in a Chinese population. Logistic regression analyses showed that the two TERT SNPs both significantly associated with cervical cancer risk in the recessive model (rs2736098, AA vs.

AG/GG: adjusted OR = 1.35, 95% CI = 1.06-1.72; rs2736100, CC vs. AC/AA: adjusted OR = 1.38, 95% CI = 1.11-1.73). However, no association was found between CLPTM1L rs402710 and cervical cancer. These results suggest that genetic variants in 5p15.33, especially in TERT, may be markers for susceptibility to cervical cancer.

摘要

无标签

端粒酶逆转录酶(TERT)rs2736098、rs2736100 和 5p15.33 上的 CLPTM1L rs402710 单核苷酸多态性(SNPs)与多种癌症的风险显著相关。然而,宫颈癌很少被评估。在这项研究中,我们在中国人群中对 1033 例宫颈癌病例和 1053 例无癌症对照进行了病例对照研究,对这三个 SNPs 进行了基因分型。逻辑回归分析表明,两个 TERT SNPs 均在隐性模型中与宫颈癌风险显著相关(rs2736098,AA 与 AG/GG:调整后的 OR = 1.35,95%CI = 1.06-1.72;rs2736100,CC 与 AC/AA:调整后的 OR = 1.38,95%CI = 1.11-1.73)。然而,CLPTM1L rs402710 与宫颈癌之间没有关联。这些结果表明,5p15.33 中的遗传变异,特别是 TERT 中的遗传变异,可能是宫颈癌易感性的标志物。

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