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A single-nucleotide polymorphism of miR-196a-2 and vitiligo: An association study and functional analysis in a Han Chinese population

机译:miR-196a-2和白癜风的单核苷酸多态性:汉族人群的关联研究和功能分析

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Recent evidence indicates that oxidative stress and genetic factors play an important role in the pathogenesis of vitiligo. SNPs in miRNAs involved in oxidative stress could potentially influence the development of vitiligo. In this case-control study, we investigated the association of a functional SNP of rs11614913 in miR-196a-2 with risk of vitiligo. A significantly lower risk of vitiligo was associated with the rs11614913 miR-196a-2 CC genotype (adjusted OR, 0.77; CI, 0.60-0.98). In addition, TYRP1 gene expression was considerably down-regulated by the rs11614913 C allele in miR-196a-2, which lowered the levels of intracellular reactive oxygen species (ROS) and reduced the proportion of early apoptosis in human melanocytes in response to H_2O_2 treatment. Our data suggest that the rs11614913 C allele in miR-196a-2 confers potential protection against oxidative effects on human melanocytes through the modulation of the target gene, TYRP1, which may account for the decreased risk of vitiligo in this study population.
机译:最近的证据表明,氧化应激和遗传因素在白癜风的发病机理中起着重要作用。 miRNA中参与氧化应激的SNP可能会影响白癜风的发生。在这个案例对照研究中,我们调查了miR-196a-2中rs11614913的功能性SNP与白癜风的风险之间的关系。 rs11614913 miR-196a-2 CC基因型与白癜风风险显着降低(校正后OR为0.77; CI为0.60-0.98)。此外,miR-196a-2中的rs11614913 C等位基因显着下调了TYRP1基因的表达,从而降低了细胞内活性氧(ROS)的水平,并降低了人类黑素细胞响应H_2O_2处理后的早期凋亡比例。我们的数据表明,miR-196a-2中的rs11614913 C等位基因可通过调节靶基因TYRP1来赋予针对人类黑素细胞氧化作用的潜在保护作用,这可能是该研究人群中白癜风风险降低的原因。

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