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一个新硝基还原酶基因NOR1编码区单核苷酸多态及与鼻咽癌的关联分析 被引量:17

Studies of Association Between Nasopharyngeal Carcinoma and Single-Nucleotide Polymorphisms in NOR1, a Novel Oxidored-nitro Domain-containing Protein Gene
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摘要 NOR1基因是中南大学湘雅医学院肿瘤研究所克隆的一个鼻咽癌表达下调新基因 ,生物信息学预测NOR1基因含有硝基还原酶结构域 ,该基因可能参与亚硝胺类化学致癌物在体内的代谢过程 ,从而与鼻咽癌的发生密切相关 .通过采用病例 对照的研究方法 ,利用测序技术对 144名鼻咽癌患者和匹配的 144名正常人NOR1基因编码区单核苷酸多态 (codingregionsinglenucleotidepolymorphisms ,cSNPs)进行基因分型 ,关联分析结果显示所检测到的两个cSNPs之间存在连锁不平衡 ,且均与鼻咽癌发病相关 ,两个cSNPs及它们所组成的单倍型相对危险度分别为 1 3 6、 1 64和 1 3 7.两个cSNPs的多态性改变均使NOR1基因编码蛋白一级结构发生了变化 ,这种改变可能影响NOR1基因编码蛋白的结构和功能 . Nasopharyngeal carcinoma (NPC) is a rare malignancy tumor in most parts of the world, while with high incidence rate in the south of China. NOR1, a NPC down-regulated gene, was newly-cloned using cDNA micro-array. NOR1 gene has an oxidored-nitro domain predicted by bioinformatics. The latest results suggest that the NOR1 gene may participate in the metabolism of chemical carcinogen such as nitrosamine in vivo. Genotype of coding region single nucleotide polymorphisms (cSNPs) in NOR1 gene were performed by sequencing in 144 unrelated NPC subjects and 144 control subjects which matched in age, sex and residence. Association analysis suggests that there is linkage disequilibrium between the 2 cSNPs, both of them associated with NPC. And the relative risk of 2 cSNPs and their haplotypes were 1.36, 1.64 and 1.37 respectively. Both of the two SNPs could change the sequence of NOR1 protein, which might influence its structure and function. The results indicated that the SNPs in NOR1 gene may play a certain role in carcinogenesis and development of NPC.
出处 《生物化学与生物物理进展》 SCIE CAS CSCD 北大核心 2003年第3期401-405,共5页 Progress In Biochemistry and Biophysics
基金 国家重点基础研究发展规划项目 ( 973) (G19980 5 10 0 8) 国家高技术"863"计划资助项目 ( 2 0 0 1AA2 2 10 31) 国家自然科学基金资助项目 ( 30 10 0 0 2 7)~~
关键词 硝基还原酶基因 NORl编码区 单核苷酸多态 鼻咽癌 关联分析 single nucleotide polymorphism,NOR1 gene,nasopharyngeal carcinoma,association analysis
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  • 1童克中.基因及其表达[M].北京:科学出版社,1998.116-144.
  • 2[1]Teng D H-F, Hu R, Lin H, et al. MMAC1/PTEN Mutations in primary tumor specimens and tumor cell lines. Cancer Research, 1997,57(23):5221~5225
  • 3[2]Hu L F, Eiriksdottir G, Lebedeva T, et al. Loss of heterozygosity on chromosome arm 3P in nasopharyngeal carcinoma. Genes, Chromosomes & Cancer, 1996, 17(2): 118~126
  • 4[3]Huang D P, Lo K W, Choi P H, et al. Loss of heterozygosity on the short arm of chromosome 3 in nasopharyngeal carcinoma. Cancer Genet Cytogenet,1991,54(1):91~99
  • 5[4]Deng L, Jing N, Tan G, et al. A common region of allelic loss on chromosome region 3p25.3~26.3 in nasopharyngeal carcinoma. Genes, Chromosomes & Cancer, 1998,23(1):21~25
  • 6[5]Vanin E F. Processed pseudogenes: characteristics and evolution.Ann Rev Genet, 1985,19:253~272
  • 7[6]Fujii G H, Morimoto A M, Berson A E, et al. Transcriptional analysis of PTEN/MMAC1 pseudogene,ΨPTEN. Oncogene, 1999, 18(9): 1765~1769
  • 8Parkin D M, Laara E, Muir C S. Estimates of the worldwide frequency of sixteen major cancers in 1980. Int J cancer, 1988,41(2): 184~197
  • 9Hildesheim A, Levine P H. Etiology of nasopharyngeal carcinoma: a review. Epidemiol Rev, 1993,15(2):466~485
  • 10Qian J, Yang J B, Li G Y, et al. Isolation and Characterization of a novel cDNA, UBAP1, derived from the tumor suppressor locus in human chromosome 9p21-22. J Cancer Res Clin Oncol, 2001, 127(10): 613~618

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