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Ataxin-3蛋白在胃癌组织中的表达及病理学特征研究

The Expression and Research of the Pathological Features for Ataxin-3 Protein in Gastric Carcinoma
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摘要 目的:研究Ataxin-3蛋白在胃癌的表达,探讨在胃癌组织病理学特征。方法:将患者标本固定、石蜡包埋、切片、免疫组化染色,通过半定量计分法判断结果,镜检采用双盲原则,由两位不同医师进行评分。结果:Ataxin-3在正常胃黏膜中主要呈中、高度表达,总阳性率为100%;在胃癌组织及上皮内瘤变主要呈低强度表达,少数呈中等强度表达,和正常胃黏膜组织相比总阳性率显著降低(P<0.01);Ataxin-3表达与患者年龄、性别、肿瘤部位及大小及临床分期无关,与Lauren组织学分型有关,与混合型及弥漫型癌患者相比,肠型胃癌患者低、中度表达显著提高(P<0.05)。结论:Ataxin-3蛋白可能与胃癌分化增殖有关,在胃癌的发生发展过程中起重要意义。 Objective :To study the expression of Ataxin-3 protein in gastric cancer and explore the histopathological features of gastric .Methods :The patient specimens were fixed ,and paraffi n-embedded ,sliced ,immunohistochemical staining ,judged by the results of semi-quantitative scoring method ,and took by the principle of microscopic double-blind ,scored by two different physicians .Results:Ataxin-3 in normal gastric mucosa was proposed high expression ,and the total positive rate was 100% .In gastric carcinoma and intraepithelial neoplasia expression ,it was with a low-inten-sity ,few showed moderate expression ,and compared with normal mucosal tissue phase ,the total positive rate was sig-nificantly lower (P〈0 .01) .Ataxin-3 expression was not connected with patient’s age ,sex ,tumor location and size , and clinical stage ,but was related with histological type and Lauren .Compared with the mixed cancer patients and pa-tients with diffuse ,the intestinal type gastric cancer in low and moderate expression was significantly increased (P〈0.05) .Conclusion:Ataxin-3 protein may be related to differentiation and proliferation of gastric cancer ,and it plays an important significance in the development of gastric cancer .
作者 何凡桂 张莉
出处 《医学理论与实践》 2014年第7期853-854,共2页 The Journal of Medical Theory and Practice
关键词 Ataxin-3蛋白 胃癌组织 表达 病理学特征 Ataxin-3 protein Gastric carcinoma Expression Pathological features
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参考文献4

  • 1Ana-Jo?o Rodrigues,Maria do Carmo Costa,Teresa-Luísa Silva,Daniela Ferreira,Fernanda Bajanca,Elsa Logarinho,Patrícia Maciel.Absence of ataxin-3 leads to cytoskeletal disorganization and increased cell death[J].BBA - Molecular Cell Research.2010(10)
  • 2Pádraig D’Arcy,Stig Linder.Proteasome deubiquitinases as novel targets for cancer therapy[J].International Journal of Biochemistry and Cell Biology.2012(11)
  • 3李忠武,曹登峰.胃癌病理分型与临床个体化治疗——问题与展望[J].中国医学前沿杂志(电子版),2012,4(5):15-20. 被引量:6
  • 4王素霞,刘媛,吴慧娟,张志刚.去泛素化酶的研究及其进展[J].临床与实验病理学杂志,2008,24(6):734-737. 被引量:18

二级参考文献26

  • 1徐德立.一种新的肿瘤抑制因子Cylindromatosis[J].细胞生物学杂志,2004,26(6):591-593. 被引量:5
  • 2Johnston S C, Riddle S M, Cohen R E,et al. Structural basis for the specificity of ubiquitin C-terminal hydrolases [ J ]. EMBO J, 2000,18 (14) : 3877 -3887.
  • 3Baek S H, Park K C, Lee J I, et al. A novel family of ubiquitin-specific proteases in chick skeletal muscle with distinct N-and C-terminal extensions[J].Biolchem J, 1998,334(Pt3) :677 -684.
  • 4Evans P C, Smith T S, Lai M J, et al. A novel type of deubiquitinating enzyme [ J ]. J Biol Chem, 2003,278 ( 25 ) : 23180 - 23186.
  • 5Scheel H, Tomiuk S, Hofmann K, et al. Elucidation of ataxin-3 and ataxin-7 function by integrative bioinformatics [ J ]. Hum Mol Genet,2003,12 (21) : 2845 -2852.
  • 6Tran H J, Allen M D, Lowe J, Bycroft M. Structure of the Jabl/ MPN domain and its implications for proteasome function[ J]. Biochemistry, 2003,42 (39) : 11460 - 11465.
  • 7Leggett D S, Hanna J, Borodovsky A, et al. Multiple associated proteins regulate proteasome structure and function[ J ]. Mol Ceils, 2002,10 (3) :495 - 507.
  • 8Schreiner P, Chen X, Husnjak K, et al. Ubiquitin docking at the proteasome through a novel pleckstrin-homology domain interaction [ J ]. Nature, 2008,453 (7194 ) :548 - 552.
  • 9Song L, Rape M. Reverse the curse-the role of deubiquitination in cell cycle control[J]. Curr Opin Cell Biol, 2008,20(2) :156 - 163.
  • 10Huang Y, Baker R T, Fischer-Vize J A. Control of cell fate by a deubiquitinating enzyme encoded by the fat facets gene [ J ]. Science,1995,270 (5243) : 1828 - 1831.

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