首页> 外文期刊>Human Molecular Genetics >Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expression
【24h】

Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expression

机译:精细定位可在5p15处确定多个前列腺癌风险基因座,其中之一与TERT表达相关

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Associations between single nucleotide polymorphisms (SNPs) at 5p15 and multiple cancer types have been reported. We have previously shown evidence for a strong association between prostate cancer (PrCa) risk and rs2242652 at 5p15, intronic in the telomerase reverse transcriptase (TERT) gene that encodes TERT. To comprehensively evaluate the association between genetic variation across this region and PrCa, we performed a fine-mapping analysis by genotyping 134 SNPs using a custom Illumina iSelect array or Sequenom MassArray iPlex, followed by imputation of 1094 SNPs in 22 301 PrCa cases and 22 320 controls in The PRACTICAL consortium. Multiple stepwise logistic regression analysis identified four signals in the promoter or intronic regions of TERT that independently associated with PrCa risk. Gene expression analysis of normal prostate tissue showed evidence that SNPs within one of these regions also associated with TERT expression, providing a potential mechanism for predisposition to disease.
机译:已经报道了5p15处的单核苷酸多态性(SNP)与多种癌症类型之间的关联。我们以前已经显示出证据,证明前列腺癌(PrCa)风险与rs2242652在5p15时有很强的联系,这是编码TERT的端粒酶逆转录酶(TERT)基因中的内含子。为了全面评估该区域的遗传变异与PrCa之间的关联,我们通过使用定制的Illumina iSelect阵列或Sequenom MassArray iPlex对134个SNP进行基因分型,然后在22301例PrCa和22320个病例中估算1094个SNP进行了精细映射分析实用协会中的控件。多元逐步逻辑回归分析确定了TERT启动子或内含子区域中与PrCa风险独立相关的四个信号。正常前列腺组织的基因表达分析表明,有证据表明这些区域之一内的SNPs也与TERT表达相关,为疾病的易感性提供了潜在的机制。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号