多种族队列研究中当前吸烟者尿镉水平的全基因组关联研究。

IF 3.1 2区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Shannon M Sullivan, Sharon E Murphy, Daniel O Stram, Lynne R Wilkens, Christopher A Haiman, Loïc Le Marchand, Irina Stepanov, S Lani Park
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引用次数: 0

摘要

背景:镉(Cd)被列为国际癌症研究机构(IARC)第一类人类致癌物,存在于香烟烟雾中。最近的研究表明,遗传在影响Cd生物标志物水平方面的潜在作用。方法:我们对来自多种族队列研究的1977名当前吸烟者进行了尿Cd水平的全基因组关联研究(GWAS),该研究包括来自五个不同种族和民族的参与者。根据收集尿液的年龄、性别、自我报告的种族/民族和前十大主要成分调整线性回归模型。结果:在分析的11 710 497个单核苷酸多态性(SNP)中,没有与尿Cd的关联达到全基因组意义(P结论:我们对不同吸烟人群的尿Cd水平的GWAS显示与SCARA5、NIPBL、SPINK4、SLC9A7和5p13.3的变异有暗示的关联。这些发现强调了遗传因素在了解和减轻与致癌物内剂量有关的健康风险方面的潜在作用,特别是在与烟草有关的致癌物的情况下。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genome-wide association study of urinary cadmium levels in current smokers from the multiethnic cohort study.

Background: Cadmium (Cd), classified as an International Agency for Research on Cancer (IARC) Group 1 human carcinogen, is present in cigarette smoke. Recent studies have illustrated the potential role of genetics in influencing Cd biomarker levels.

Methods: We conducted a genome-wide association study (GWAS) of urinary Cd levels in 1977 current smokers from the Multiethnic Cohort Study, comprising participants from five different racial and ethnic groups. Linear regression models were adjusted for age at urine collection, sex, self-reported race/ethnicity, and the top ten leading principal components.

Results: Among the 11 710 497 single nucleotide polymorphisms (SNP) analyzed, no associations with urinary Cd reached genome-wide significance (P < 5.0 × 10-8). Notably, five variants demonstrated suggestive associations with urinary Cd levels (P < 1.0 × 10-6). Lead variants included: rs10097646 in the SCARA gene at 8q13.2 (P = 2.62 × 10-7); rs7444817 in the NIPBL gene at 5p13.2 (P = 3.10 × 10-7), rs830422 in the SPINK4 gene at 9q13.2 (P = 4.89 × 10-7); chrX:145489901 in the SLC9A7 gene at Xq121.1 (P = 5.38 × 10-7); and rs73074456 at 5p13.3 (P = 5.86 × 10-7).

Conclusions: Our GWAS of urinary Cd levels in a diverse population of people who smoke, revealed suggestive associations with variants in SCARA5, NIPBL, SPINK4, SLC9A7, and 5p13.3. These findings underscore the potential role of genetic factors in understanding and mitigating the health risks associated with internal dose of carcinogens, particularly in the context of tobacco-related carcinogens.

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来源期刊
Human molecular genetics
Human molecular genetics 生物-生化与分子生物学
CiteScore
6.90
自引率
2.90%
发文量
294
审稿时长
2-4 weeks
期刊介绍: Human Molecular Genetics concentrates on full-length research papers covering a wide range of topics in all aspects of human molecular genetics. These include: the molecular basis of human genetic disease developmental genetics cancer genetics neurogenetics chromosome and genome structure and function therapy of genetic disease stem cells in human genetic disease and therapy, including the application of iPS cells genome-wide association studies mouse and other models of human diseases functional genomics computational genomics In addition, the journal also publishes research on other model systems for the analysis of genes, especially when there is an obvious relevance to human genetics.
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