期刊文献+

EMP-1基因在喉癌中的表达差异分析 被引量:6

Differential Expression of the Epithelial Membrane Protein1of Laryngeal Carcinoma
下载PDF
导出
摘要 目的分析上皮膜蛋白-1(epithelialmembraneprotein-1,EMP-1)基因在喉癌中的表达差异,以进一步探讨喉癌的发病机制。方法用微阵列分析技术分析喉癌基因的差异表达情况,选取其中之一的EMP-1基因,用半定量逆转录酶-聚合酶链反应(reversetranscriptasepolymerasechainreaction,RT-PCR)技术分析EMP-1基因在不同类型喉癌中的表达情况,数据分析采用SPSS软件。结果EMP-1基因在不同类型配对喉癌中皆呈低表达,明显低于相应的正常喉粘膜组织(P<0.05),EMP-1基因表达量与喉癌的分化类型、分期无明显关系(P>0.05)。结论EMP-1基因与喉癌的发病明显相关,揭示这种关系将有助于探讨喉癌的发病机制。 Objective In order to explore pathogenic mechanism of laryngeal carcinoma,the involved genes were identified in larynx carcinogenesis by comparing the gene expression profile in matched primary normal epithelial cells and primary laryngeal carcinoma cells from the same patients.Methods A cDNA microarray analysis consisting of11431human genes revealed signi -ficant changes in the expression of35genes,with8genes being up-regulated and27being down-regulated.The epithelial membrane protein-1(EMP -1)is one of the down-regulated genes.EMP -1expression in various kinds of laryngeal carcinoma was determined by semi -quantitative reverse transcriptase polymerase chain reaction (qRT-PCR).Results The EMP -1mRNA levels in all laryngeal carcinoma cells was significantly lower than that in the matched primary normal epithelial cells(P<0.05)and were not correlated to the stage and differentiation of laryngeal carcinoma (P>0.05).Conclusions The EMP -1expression was correlated to larynx carcinogenesis and may be helpful to elucidate the pathogenic mechanism in laryngeal carcinoma.
出处 《中国医学科学院学报》 CAS CSCD 北大核心 2003年第1期47-51,共5页 Acta Academiae Medicinae Sinicae
基金 国家自然科学基金(30170519)~~
关键词 喉癌 上皮膜蛋白-1基因 逆转录酶-聚合酶链反应 cDNA微阵列分析 laryngeal carcinoma epithelial membrane protein-1 reverse transcriptase polymerase chain reaction microarray analysis
  • 相关文献

参考文献15

  • 1Shal JP;Karnell LH;Hoffman HT.Patterns of cancer for cancer of the larynx in the United States,1997.
  • 2Narayana A;Vaughan AT;Fisher SG.Second primary tumors in laryngeal cancer: results of long-term follow-up[J],1998(03).
  • 3Schena M;Shalon D;Davis RW.Quantitative monitoring of gene expression patterns with a complementary DNA microarray[J],1995(5235).
  • 4Sehgal A;Boynton AL;Young RF.Application of the differential hybridization of Atlas Human expression arrays technique in the identification of differentially expressed genes in human glioblastoma multiforme tumor tissue[J],1998(04).
  • 5DeRisi J;Penland L;Brown PO.Use of a cDNA micro ar ray to analyse gene expression patterns in human cancer[J],1996(04).
  • 6Ben Porath Ⅰ;Benvenisty N.Characterization of a tumorassociated gene,a member of a novel family of genes encoding membrane glycoproteins[J],1996(1-2).
  • 7Ben Porath Ⅰ;Yanuka O;Benvenisty N.The tmp gene, encoding a membrane protein, is a c-Myc target with a tumorigenic activity[J],1999(05).
  • 8Xu L;Hui LJ;Hu GX.Expression profiling suggested a regulatory role of liver-enriched transcription facts in human hepatocellular carcinoma,2001.
  • 9Taylor V;Welcher AA;Program AE.Epithelial membrane protein-1, peripheral myelin 22, and lens membrane protein 20 define a novel gene family[J],1995(48).
  • 10Gnirke AU;Weidle UH.Investigation of prevalence and regulation of expression of progression associated protein (PAP),1998(18).

二级参考文献7

  • 1Taylor V, Welcher AA, Program AE, et al. Epithelial membrane protein-1, peripheral myelin protein 22, and lens membrane protein 20 define a novel gene family [J]. J Biol Chem, 1995, 270(48):28824-28833.
  • 2Gnirke AU, Weidle UH. Investigation of prevalence and regulation of expression of progression associated protein (PAP)[J]. Anticancer Res, 1998, 18(6A):4363-4369.
  • 3Chen Y, Medvedev A, Ruzanov P, et al. cDNA cloning, genomic structure, and chromosome mapping of the human epithelial membrane protein CL-20 gene (EMP1), a member of the PMP22 family [J]. Genomics, 1997, 41(1):40-48.
  • 4萨姆布鲁克,弗里奇,曼尼阿斯蒂.分子克隆实验指南[M].第二版.科学出版社,1992:870-873.
  • 5Lobsiger CS, Magyar JP, Taylor V, et al. Identification and characterization of a cDNA and the structural gene encoding the mouse epithelial membrane protein-1 [J]. Genomics, 1996,36(3):379-387.
  • 6Taylor V, Suter U. Epithelial membrane protein-2 and epithelial membrane protein-3: two novel members of the peripheral myelin protein 22 gene family [J]. Gene, 1996, 175(1-2):115-120.
  • 7Ben-Porath I, Yanuka O, Benvensity N. The tmp gene, encoding a membrane protein, is a c-Myc target with a tumorigenic activity [J]. Mol Cell Boil, 1999, 19(5):3529-3539.

共引文献23

同被引文献25

  • 1王涛,刘晓媛,赵继宗,张淑珍.异丙酚对全脑缺血再灌注损伤大鼠的脑保护作用及其机制研究[J].中国康复理论与实践,2004,10(8):464-465. 被引量:7
  • 2王金光,郑启新,王运涛,赵铭,郭晓东.重组人红细胞生成素对大鼠脊髓损伤后神经细胞凋亡的保护作用[J].中国康复理论与实践,2005,11(2):84-86. 被引量:1
  • 3李纪鹏,王为忠,凌瑞,陈冬利,李孟彬,刘季.大鼠小肠缺血再灌注后氧自由基改变及肝脏Bax、Bcl-2、p53的表达[J].中国康复理论与实践,2005,11(3):189-191. 被引量:6
  • 4Chen Z Y, Corey D P. Understanding inner ear development with gene expression profiling [J]. J Neurobiol, 2002,53(2) :276-285.
  • 5Morris K A, Snir E, Pompeia C, et al. Differential expression of genes within the cochlea as defined by a custom mouse inner ear microarray [J]. J Assin Res Otolaryngol, 2005,6( 1 ) :75-89.
  • 6Iijima N, Suzuki N, Oguchi T, et al. The effect of hypergravity on the inner ear: CREB and syntaxin are up-regulated [J]. Neuroreport, 2004,15(6) :965-969.
  • 7Lin J, Ozeki M, Javel E, et al. Identification of gene expression profiles in rat ears with cDNA microarrays [J]. Hear Res, 2003,175(1-2) :2-13.
  • 8Abe S, Katagiri T, Saito-Hisaminato A, et al. Identification of CRYM as a candidate responsible for nonsyndromic deafness, through cDNA microarray analysis of human cochlear and vestibular tissues [J]. Am J Hum Genet, 2003,72( 1 ) :73-82.
  • 9Previati M, Lanzoni I, Corbacella E, et al. RNA expression induced by cisplatin in an organ of Corti-defived immortalized cell line [J]. Hear Res, 2004,196(1-2) :8- 18.
  • 10Nagy I, Bodmer M, Brors D, et al. Early gene expression in the organ of Corti exposed to gentamicin [J]. Hear Res, 2004,195(1-2) : 1-8.

引证文献6

二级引证文献17

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部