Sullivan Shannon M, Murphy Sharon E, Stram Daniel O, Wilkens Lynne R, Haiman Christopher A, Le Marchand Loïc, Stepanov Irina, Park S Lani
Department of Laboratory Medicine and Pathology, University of Minnesota, 1200 Washington Ave S Suite 175, Minneapolis, MN 55415, United States.
Division of Environmental Health Sciences, School of Public Health, University of Minnesota, 1260 Mayo Building, MMC 807420 Delaware St. SE Minneapolis, MN 55455, United States.
Hum Mol Genet. 2025 Mar 20;34(7):611-616. doi: 10.1093/hmg/ddae202.
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.
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.
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).
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.
镉(Cd)被国际癌症研究机构(IARC)列为1类人类致癌物,存在于香烟烟雾中。最近的研究表明基因在影响镉生物标志物水平方面具有潜在作用。
我们对多民族队列研究中的1977名当前吸烟者的尿镉水平进行了全基因组关联研究(GWAS),该队列包括来自五个不同种族和民族的参与者。线性回归模型针对尿液采集时的年龄、性别、自我报告的种族/民族以及前十大主要成分进行了调整。
在分析的11710497个单核苷酸多态性(SNP)中,没有与尿镉的关联达到全基因组显著性(P < 5.0×10⁻⁸)。值得注意的是,有五个变异体显示出与尿镉水平有提示性关联(P < 1.0×10⁻⁶)。主要变异体包括:8q13.2处SCARA基因中的rs10097646(P = 2.62×10⁻⁷);5p13.2处NIPBL基因中的rs7444817(P = 3.10×10⁻⁷),9q13.2处SPINK4基因中的rs830422(P = 4.89×10⁻⁷);Xq121.1处SLC9A7基因中的chrX:145489901(P = 5.38×10⁻⁷);以及5p13.3处的rs73074456(P = 5.86×10⁻⁷)。
我们对不同吸烟人群尿镉水平的GWAS研究揭示了与SCARA5、NIPBL、SPINK4、SLC9A7和5p13.3变异体的提示性关联。这些发现强调了遗传因素在理解和减轻与致癌物内部剂量相关的健康风险方面的潜在作用,特别是在烟草相关致癌物的背景下。