5个中国人群白细胞免疫球蛋白样受体A3基因缺失与鼻咽癌的保护性关联

IF 2.3 4区 医学 Q3 GENETICS & HEREDITY
Wei Tian, Li Xin Li, Wen Cheng, He Kun Jin, Sha Shuang Zhang
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引用次数: 0

摘要

在位于19q13.4的13个白细胞igg样受体(LILR)位点中,LILRA3的独特之处在于它编码一个缺乏跨膜和细胞质结构域的可溶性蛋白,并且在一些人类个体中检测到跨越前7个外显子的6.7 kb缺失。目前,缺乏关于LILRA3基因缺失在更多样化的族群中的分布的数据。此外,LILRA3拷贝数变异(copy number variation, CNV)与鼻咽癌(NPC)的相关性也未见相关研究。本研究选取了来自中国大陆的5个种群:湖南(N = 1478)和广东(N = 107)两个南方汉族种群;福建省东南部汉族1人(N = 439);采用聚合酶链反应-序列特异性引物(PCR-SSP)方法,对内蒙古汉族(N = 104)和内蒙古蒙古族(N = 158) 2个北方人群的LILRA3基因CNV进行了检测。LILRA3变异也在湖南汉族人群鼻咽癌病例队列(N = 1142)中进行了检测。在5个中国人群中,LILRA3基因缺失形式(LILRA3*Del)的频率向北增加(p值均< 0.05)。群体间比较也揭示了LILRA3基因CNV在现代人群中的分布存在显著差异。LILRA3*Del基因可显著降低湖南汉族人群鼻咽癌发病风险(等位基因水平:OR = 0.79, 95% CI = 0.71-0.89, p < 0.0001;在基因型水平:OR = 0.63, 95% CI = 0.51-0.79, p < 0.0001)。LILRA3变异与HLA-A*02:07、HLA-A*11:01、HLA-B*13和HLA-B*46:01等位基因无交互作用。我们的研究首次证明了LILRA3基因在中国南方人群中与鼻咽癌易感性相关。未来对其他人群的独立研究有必要证实本研究报告的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Leukocyte immunoglobulin-like receptor A3 gene deletion in five Chinese populations and protective association with nasopharyngeal carcinoma

Among the thirteen leukocyte Ig-like receptor (LILR) loci located at 19q13.4, LILRA3 is unique in that it encodes a soluble protein lacking the transmembrane and cytoplasmic domains, and a 6.7 kb deletion spanning the first seven exons has been detected in some human individuals. Presently, there is a lack of data about the distribution of LILRA3 gene deletion in more diverse ethnic groups. Also, no previous studies have investigated the correlation between copy number variation (CNV) of LILRA3 and nasopharyngeal carcinoma (NPC). In this study, five populations from China mainland: two Southern Han populations, Hunan (N = 1478) and Guandong (N = 107); one Southeastern Han population, Fujian (N = 439); and two Northern populations, Inner Mongolia Han (N = 104) and Mongol population from Inner Mongolia (N = 158) were investigated for CNV of LILRA3 using polymerase chain reaction-sequence-specific priming (PCR-SSP) method. LILRA3 variants were also examined in a cohort of NPC cases (N = 1142) in Hunan Han population. The five Chinese populations demonstrated northward increase in frequency of the deleted form of LILRA3 gene (LILRA3*Del) (all corrected p values < 0.05). Inter-population comparison also uncovered significant differentiation in the distribution of CNV of LILRA3 among modern human populations. LILRA3*Del was found to confer significantly reduced risk to NPC in Hunan Han population (at allelic level: OR = 0.79, 95% CI = 0.71–0.89, p < 0.0001; at genotype level: OR = 0.63, 95% CI = 0.51–0.79, p < 0.0001). No interaction was found between LILRA3 variants and HLA-A*02:07, HLA-A*11:01, HLA-B*13 and HLA-B*46:01 alleles in susceptibility to NPC. Our study constitutes the first demonstration of LILRA3 gene as a locus linked to NPC susceptibility in a southern Chinese population. Future independent studies in other populations are warranted to confirm the findings reported in this study.

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来源期刊
CiteScore
4.70
自引率
0.00%
发文量
48
审稿时长
6-12 weeks
期刊介绍: The International Journal of Immunogenetics (formerly European Journal of Immunogenetics) publishes original contributions on the genetic control of components of the immune system and their interactions in both humans and experimental animals. The term ''genetic'' is taken in its broadest sense to include studies at the evolutionary, molecular, chromosomal functional and population levels in both health and disease. Examples are: -studies of blood groups and other surface antigens- cell interactions and immune response- receptors, antibodies, complement components and cytokines- polymorphism- evolution of the organisation, control and function of immune system components- anthropology and disease associations- the genetics of immune-related disease: allergy, autoimmunity, immunodeficiency and other immune pathologies- All papers are seen by at least two independent referees and only papers of the highest quality are accepted.
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