...
首页> 外文期刊>Human Genetics >Interactions between household air pollution and GWAS-identified lung cancer susceptibility markers in the Female Lung Cancer Consortium in Asia (FLCCA)
【24h】

Interactions between household air pollution and GWAS-identified lung cancer susceptibility markers in the Female Lung Cancer Consortium in Asia (FLCCA)

机译:亚洲女性肺癌协会(FLCCA)中的家庭空气污染与GWAS鉴定的肺癌易感性指标之间的相互作用

获取原文
获取原文并翻译 | 示例
           

摘要

We previously carried out a multi-stage genome-wide association study (GWAS) on lung cancer among never smokers in the Female Lung Cancer Consortium in Asia (FLCCA) (6,609 cases, 7,457 controls) that identified novel susceptibility loci at 10q25.2, 6q22.2, and 6p21.32, and confirmed two previously identified loci at 5p15.33 and 3q28. Household air pollution (HAP) attributed to solid fuel burning for heating and cooking, is the leading cause of the overall disease burden in Southeast Asia, and is known to contain lung carcinogens. To evaluate the gene-HAP interactions associated with lung cancer in loci independent of smoking, we analyzed data from studies participating in FLCCA with fuel use information available (n = 3; 1,731 cases; 1,349 controls). Coal use was associated with a 30 % increased risk of lung cancer (OR 1.3, 95 % CI 1.0-1.6). Among the five a priori SNPs identified by our GWAS, two showed a significant interaction with coal use (HLA Class II rs2395185, p = 0.02; TP63 rs4488809 (rs4600802), p = 0.04). The risk of lung cancer associated with coal exposure varied with the respective alleles for these two SNPs. Our observations provide evidence that genetic variation in HLA Class II and TP63 may modify the association between HAP and lung cancer risk. The roles played in the cell cycle and inflammation pathways by the proteins encoded by these two genes provide biological plausibility for these interactions; however, additional replication studies are needed in other non-smoking populations.
机译:我们之前对亚洲女性肺癌协会(FLCCA)从未吸烟者进行了肺癌的多阶段全基因组关联研究(GWAS)(6,609例病例,7,457例对照),该研究在10q25.2处确定了新的易感基因座, 6q22.2和6p21.32,并在5p15.33和3q28确认了两个先前确定的基因座。家庭空气污染(HAP)归因于加热和烹饪过程中燃烧固体燃料,是东南亚总体疾病负担的主要原因,并且已知含有肺致癌物。为了评估与吸烟独立的基因座中的肺癌相关的基因-HAP相互作用,我们分析了参与FLCCA研究的数据并提供了可用的燃料使用信息(n = 3; 1,731例; 1,349例对照)。煤炭使用会增加30%的肺癌风险(OR 1.3,95%CI 1.0-1.6)。在我们的GWAS确定的五个先验SNP中,两个显示出与煤炭使用之间的显着相互作用(HLA II类rs2395185,p = 0.02; TP63 rs4488809(rs4600802),p = 0.04)。这两个SNP的等位基因与煤暴露相关的肺癌风险有所不同。我们的观察提供了证据,表明HLA II类和TP63类的遗传变异可能会改变HAP与肺癌风险之间的关联。这两个基因编码的蛋白质在细胞周期和炎症途径中发挥的作用为这些相互作用提供了生物学上的可信度。但是,在其他非吸烟人群中还需要进行其他复制研究。

相似文献

  • 外文文献
  • 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