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

被引:20
|
作者
Huang, Ye [1 ,2 ,3 ]
Yi, Xiuli [1 ]
Jian, Zhe [1 ]
Wei, Chao [1 ]
Li, Shuli [1 ]
Cai, Chuan [1 ,2 ]
Zhang, Ping [2 ]
Li, Kai [1 ]
Guo, Sen [1 ]
Liu, Ling [1 ]
Shi, Qiong [1 ]
Gao, Tianwen [1 ]
Li, Chunying [1 ]
机构
[1] Fourth Mil Med Univ, Xijing Hosp, Dept Dermatol, Xian 710032, Peoples R China
[2] Gen Hosp AF, Dept Dermatol, Beijing, Peoples R China
[3] Inst Aviat Med, Affiliated Hosp, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
oxidative stress; miR-196a-2; SNP; vitiligo; TYRP1; TYROSINASE-RELATED PROTEIN-1; CELL LUNG-CANCER; OXIDATIVE STRESS; AUTOIMMUNE-DISEASES; GENETIC-VARIANTS; MICRORNAS; MELANOCYTES; EXPRESSION; RISK; H2O2;
D O I
10.1111/pcmr.12081
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 casecontrol 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, 0.600.98). 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 H2O2 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.
引用
收藏
页码:338 / 347
页数:10
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