Article Summary
张先娇,苗 毅,曲书毅,杨 城,谢祥军,刘寒强,王水利.TLR4基因rs10983755位点单核苷酸多态性与非小细胞肺癌易感性的相关性研究[J].现代生物医学进展英文版,2018,(4):701-704.
TLR4基因rs10983755位点单核苷酸多态性与非小细胞肺癌易感性的相关性研究
Correlative Analysis between SNP rs10983755 in TLR4 Gene and NSCLC Susceptibility
Received:October 12, 2017  Revised:October 30, 2017
DOI:10.13241/j.cnki.pmb.2018.04.021
中文关键词: Toll样受体4  单核苷酸多态性  非小细胞肺癌
英文关键词: Toll-like receptors 4  Single nucleotide polymorphism  Non-small cell lung cancer
基金项目:陕西省自然科学基金项目(2014JQ4130)
Author NameAffiliationE-mail
张先娇 陕西省人民医院西安医学院附属医院 陕西 西安710068 zhangxianjiaovip@163.com 
苗 毅 陕西省人民医院西安医学院附属医院 陕西 西安710068  
曲书毅 第四军医大学军事预防医学院 陕西 西安 710032  
杨 城 第四军医大学军事预防医学院 陕西 西安 710032  
谢祥军 第四军医大学军事预防医学院 陕西 西安 710032  
刘寒强 第四军医大学军事预防医学院 陕西 西安 710032  
王水利 陕西省人民医院西安医学院附属医院 陕西 西安710068  
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中文摘要:
      摘要 目的:探讨TLR4基因rs10983755 A/G单核苷酸多态性(SNP)与非小细胞肺癌(NSCLC)易感性的相关性。方法:采用病例-对照研究方法纳入160例非小细胞肺癌患者(NSCLC组)和160例健康对照(NC组),利用MassARRAY飞行时间质谱生物芯片系统对TLR4 基因rs10983755位点的单核苷酸多态性进行分型检测,并进行统计学分析。结果:rs10983755等位基因频率在中国汉族NSCLC患者和健康人群中的分布差异具有统计学意义(P<0.05),A等位基因携带者NSCLC发生风险是G等位基因携带者的1.821倍(95% CI=1.124~2.906);rs10983755基因型频率在NSCLC患者和健康人群中分布差异具有统计学意义(P<0.05),AA+AG基因型NSCLC发生风险是GG基因型的2.103倍(95% CI=1.118~3.898)。结论:TLR4基因rs10983755 A/G单核苷酸多态性与NSCLC的易感性显著相关,A是风险等位基因。
英文摘要:
      ABSTRACT Objective: To investigate the correlation of rs10983755 A/G SNP of TLR4 with non-small cell lung cancer (NSCLC) susceptibility in a population in Shaanxi province. Methods: Based on case-control study, MassARRAY platform which based on MALDI-TOF mass spectrometry technology was used to identify the genotypes of rs10983755 of TLR4 gene in 160 cases of NSCLC patients and 160 cases of healthy control in a population in Shaanxi province. Then, we did statistics analysis with epidemiological data and clinical data to find the association of SNP with NSCLC susceptibility. Results: There was a significant difference in the genotypes of the TLR4 SNP rs10983755 between the NSCLC patients and controls (P<0.05). NSCLC patients with the A allele showed a significantly higher risk of NSCLC (P<0.05) compared with the G allele, indicating that the A allele SNP rs10983755 was associated with NSCLC risk (OR=1.821, 95% CI=1.124~2.906). Compared with GG genotype, AA+AG genotype was significantly associated with increased risk of NSCLC (OR=2.103, 95% CI=1.118~3.898). Conclusion: The single nucleotide polymorphism of the rs10983755 of TLR4 gene was correlated with NSCLC susceptibility in a population in Shaanxi province,and the allele A was a risk allele.
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