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缺氧诱导因子-1α基因G1790A或导致COPD易感性 被引量:1

HIF-1α polymorphisms G1790A may lead to susceptibility to chronic obstructive pulmonary disease
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摘要 目的:探讨HIF-1α基因多态性于与COPD易感性之间的关系。方法:利用RT-PCR、Western blot、ELISA检测COPD病例组和对照组(各16例)人群肺组织标本中HIF-1a mRNA及HIF-1a蛋白的表达水平。利用PCR-RFLP检测COPD病例组(120例)及健康对照组(112例)人群HIF-1α基因C1772T和G1790A的多态性分布;结果:RT-PCR结果显示HIF-1a mRNA在对照组和病例组中表达无差异(P>0.05);Western blot和ELISA检测结果示对照组HIF-1α蛋白表达高于病例组(P0.05),G1790A基因型频率分布有差异(P〈0.05)。结论:HIF-1α基因G1790A单核苷酸多态性或导致COPD病人易感, Purpose: To explore whether hypoxia-inducible factor-1α (HIF-1α) polymorphisms are associated with susceptibility to chronic obstructive pulmonary disease (COPD). Materials and Methods: Sixteen patients with and sixteen healthy patients were conducted with Real time PCR、Western blot、ELISA to test the HIF-1α mRNAand HIF-1a protein levels.One hundred twenty patients with COPD and 112 healthy controls were recruited from the Han population in Southern China. PCR-RFLP was used to assess C1772T and G1790A polymorphisms of the HIF-1α gene, and differences of genotypes between the two groups were compared. Results: RT-PCR results show that HIF-1a mRNA level of control group is higher than in the group of COPD, with a t-test p〉0.05. Western blot and ELISA results indicated the hIF-1α protein level is higher in control group than in COPD group ,with a P0.05). In contrast, distributions of G1790A polymorphisms were significantly different between the two groups (P〈0.05).
出处 《国际呼吸杂志》 2016年第16期1209-1214,共6页 International Journal of Respiration
基金 广东省科学基金资助项目(20098030801247)
关键词 缺氧诱导因子-1α(HIF-1α) 慢性阻塞性肺疾病(COPD) G1790A SNP 易感性 hypoxia-inducible factor-1α (HIF-1α) chronic obstructive pulmonary disease (COPD) SNP
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  • 1Mullikin JC,Hunt SE,Cole CC,et al.An SNP map of human chromosome 22.Nature,2002;407(6803):516
  • 2Ollerenshow M,Page T,hammonds T,et al.Polymorphisms in the hypoxia inducible factor-1α gene (HIF-1α) are associated with the renal cell carcinoma phenotype.Cancer Genetics and Cytogenetics,2004;153:122
  • 3Tanimoto K,Yoshiga K,Eguchi H,et al.Hypoxia-inducible factor-1α polymorphisms associated with enhanced transactivation capacity,implying clinical significance.Carcinogenesis,2003;24(11):1779
  • 4Min JH,Yang H,Ivan M,et al.Structure of an HIF-1 alpha-pVHL complex:hydroxyproline recognition in signaling.Science,2002,296(5574):1886
  • 5Suzuki K,Kizaki T,Hitomi Y,et al.Genetic variation in hypoxia-inducible factor 1 and its possible association with high altitude adaptation in Sherpas.Medical Hypotheses,2003;61(3):385
  • 6Percy MJ,Mooney SM,Mcmullin MF,et al.A common polymorphism in the oxygen-dependent degradation domain (ODD) of hypoxia inducible factor-1α (HIF-1α) does not impair Pro-564 hydroxylation.Molecular Cancer,2003;2:31
  • 7Li d,Hirsila M,Koivunen P,et al.Many amino acid substitutions in a hypoxia-inducible transcription factor (HIF)-1α-like peptide cause only minor change in its hydroxylation by the HIF proly 4-hydroxylases.The Journal of Biological Chemistry,2004;279(59):55051
  • 8Fu X,Choi E,Bubley GJ,et al.Identification of hypoxia-inducible factor-1α (HIF-1α) polymorphism as a-mutation in prostate cancer that prevents normoxia-induced degradationg.The Prostate,2005;63:215
  • 9Semenza GL.HIF-1 and human disease:one highly involved factor.Genes & Development,2000;14:1983
  • 10Mortimer H,Patel S,Peacock AJ.The genetic basis of high-altitude pulmonary oedema.Pharmacology & Therapeutics,2004;101:183

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