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IL1RN基因多态性与脑胶质瘤患病风险的相关性

李国林 李超 李峰

李国林, 李超, 李峰. IL1RN基因多态性与脑胶质瘤患病风险的相关性[J]. 昆明医科大学学报, 2018, 39(04): 47-51.
引用本文: 李国林, 李超, 李峰. IL1RN基因多态性与脑胶质瘤患病风险的相关性[J]. 昆明医科大学学报, 2018, 39(04): 47-51.
Li Guo Lin , Li Chao , Li Feng . The Research of Correlation of Genetic Polymorphisms in IL1RN with Risk of Glioma[J]. Journal of Kunming Medical University, 2018, 39(04): 47-51.
Citation: Li Guo Lin , Li Chao , Li Feng . The Research of Correlation of Genetic Polymorphisms in IL1RN with Risk of Glioma[J]. Journal of Kunming Medical University, 2018, 39(04): 47-51.

IL1RN基因多态性与脑胶质瘤患病风险的相关性

基金项目: 

基金: 陕西省科技攻关基金资助项目 (2016SF-110);

The Research of Correlation of Genetic Polymorphisms in IL1RN with Risk of Glioma

Funds: 

基金: 陕西省科技攻关基金资助项目 (2016SF-110);

  • 摘要: 目的 研究IL1RN基因多态性与脑胶质瘤患病风险的相关性.方法 选择2012年1月至2016年12月于铜川矿务局中心医院就诊的符合入选条件的脑胶质瘤患者共200例, 以及健康对照人群200例, 分别采集血样.采用Mass ARRAY方法对rs17042888、rs315919、rs928940、rs3181052、rs452204和rs4252019六个位点的基因型进行测定, 用SPSS软件统计基因多态性与脑胶质瘤患病风险的相关性.结果 比较各位点的等位基因频率, 发现IL1RN基因上的rs315919位点的等位基因“G”和rs4252019位点的等位基因“C”会显著降低脑胶质瘤的患病风险 (rs315919:OR=0.841, 95%CI为0.7120.993, P=0.041;rs4252019:OR=0.835, 95%CI为0.7070.987, P=0.034) .引入遗传模型后, rs315919位点在隐性模型下, 携带G/G基因型的个体脑胶质瘤患病风险显著降低, 是携带T/T和G/T基因型的0.75倍 (OR=0.75, 95%CI为0.520.96, P=0.026) ;rs4252019位点在显性模型下, 携带C/T和C/C基因型的个体脑胶质瘤患病风险显著降低, 是携带T/T基因型的0.76倍 (OR=0.76, 95%CI为0.590.97, P=0.025) .结论 IL1RN基因上rs315919和rs4252019两个位点与降低脑胶质瘤的患病风险具有相关性.
  • [1] [1]MCNEILL K A.Epidemiology of brain tumors[J].Neurologic Clinics, 2016, 34 (4) :981.
    [2] [2]GOLDBRUNNER R H, BERNSTEIN J J, TONN J C.ECM-mediated glioma cell invasion[J].Microscopy Research&Technique, 2015, 43 (3) :250-257.
    [3]李小平.一个新的交叉学科:环境暴露学[J].国外医学医学地理分册, 2016, 37 (2) :81-84.
    [4] [4]WALSH K M, ANDERSON E, HANSEN H M, et al.Analysis of 60 reported glioma risk SNPs replicates published GWAS findings but fails to replicate associations from published candidate-gene studies[J].Genetic Epidemiology, 2013, 37 (2) :222.
    [5] [5]BALASUBRAMANIAN S P, AZMY I, HIGHAM S E, et al.Interleukin gene polymorphisms and breast cancer:A case control study and systematic literature review[J].Bmc Cancer, 2006, 6 (1) :188.
    [6] [6]COUSSENS L M, WERB Z.Inflammation and cancer[M].New Jersey:Humana Press, 2002:860-867.
    [7] [7]CHEN X, XU Y, CAO X, et al.Associations of Il-1family-related polymorphisms with gastric cancer risk and the role of mir-197 In Il-1f5 expression[J].Medicine, 2015, 94 (47) :e1982.
    [8] [8]SOL X, GUIN E, VALLS J, et al.SNPStats:A web tool for the analysis of association studies[J].Bioinformatics, 2006, 22 (15) :1928-1929.
    [9] [9]OZBABACAN S E A, GURSOY A, NUSSINOV R, et al.The structural pathway of interleukin 1 (IL-1) initiated signaling reveals mechanisms of oncogenic mutations and SNPs in inflammation and cancer[J].PLo S Computational Biology, 2014, 10 (2) :e1003470.
    [10] [10]GERMANO G, ALLAVENA P, MANTOVANI A.Cytokines as a key component of cancer-related inflammation[J].Cytokine, 2008, 43 (3) :374.
    [11] [11]SOLINAS G, GERMANO G, MANTOVANI A, et al.Tumor-associated macrophages (TAM) as major players of the cancer-related inflammation[J].Journal of Leukocyte Biology, 2010, 41 (34) :1065.
    [12] [12]ZHAO J, BULEK K, GULEN M F, et al.Human colon tumors express a dominant-negative form of SIGIRR that promotes inflammation and colitis-associated colon cancer in mice[J].Gastroenterology, 2015, 149 (7) :1860-1871.
    [13] [13]ALI R A, SABER L M, AL-HARBI A M.A novel association between IL1-Ra (receptor antagonist) gene polymorphism and T1DM in Al-Madina Al-Mounawra[J].European Review for Medical&Pharmacological Sciences, 2015, 19 (19) :3701.
    [14] [14]MCLEAN M H, EL-OMAR E M.Genetics of gastric cancer[J].Nat Rev Gastroenterol Hepatol, 2014, 11 (11) :664-674.
    [15] [15]III H D H, PURDUE M P, WANG S S, et al.A pooled analysis of three studies evaluating genetic variation in innate immunity genes and non-Hodgkin lymphoma risk[J].British Journal of Haematology, 2011, 152 (6) :721-726.
    [16] [16]BENSEN J T, LANGEFELD C D, HAWKINS G A, et al.Nucleotide variation, haplotype structure, and association with end-stage renal disease of the human interleukin-1gene cluster[J].Genomics, 2003, 82 (2) :194-217.
    [17] [17]BUCKHAM T A, MCKNIGHT A J, BENEVENTE D, et al.Evaluation of five interleukin genes for association with end-stage renal disease in white Europeans[J].American Journal of Nephrology, 2010, 32 (2) :103-108.
    [18] [18]JUNG M Y, KANG S W, KIM S K, et al.The interleukin-1 family gene polymorphisms in Korean patients with rheumatoid arthritis[J].Scandinavian Journal of Rheumatology, 2010, 39 (3) :190-196.
    [19] [19]OH I H, OH C, KIM H J, et al.Genetic associations of IL1RN polymorphisms with metabolic syndrome in a Korean population[J].Exp Clin Endocrinol Diabetes, 2010, 118 (5) :333.
    [20] [20]HAHN W H, CHO BSKIMS D.Interleukin-1 cluster gene polymorphisms in childhood Ig A nephropathy[J].Pediatric Nephrology, 2009, 24 (7) :1329-1336.
    [21] [21]WU X, KONDRAGUNTA V, KORNMAN K S, et al.IL-1 receptor antagonist gene as a predictive biomarker of progression of knee osteoarthritis in a population cohort[J].Osteoarthritis&Cartilage, 2013, 21 (7) :930.
    [22] [22]VAN M R, WETTINGER S B, DE VISSER M C, et al.Haplotypes of the interleukin-1 receptor antagonist gene, interleukin-1 receptor antagonist m RNA levels and the risk of myocardial infarction[J].Atherosclerosis, 2009, 203 (1) :201-205.
    [23] [23]ABHIMANYU, MRIDULA B, PANKAJ J.Footprints of genetic susceptibility to pulmonary tuberculosis:Cytokine gene variants in north Indians[J].Indian Journal of Medical Research, 2012, 135 (5) :763.
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  • 收稿日期:  2017-11-21

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