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胃癌组织中S100A11、MMP-9及E-cadherin的表达及意义 被引量:6

Significance and expression of S100A11,MMP-9 and E-cadherin in gastric cancer
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摘要 目的探讨胃癌组织中S100钙结合蛋白A11(S100A11)、基质金属蛋白酶-9(MMP-9)及E-钙黏蛋白(E-cadherin)的表达及意义。方法回顾性研究采用免疫组化法检测收集的92例胃癌组织及92例癌旁正常组织中S100A11、MMP-9及E-cadherin的表达,并分析三者与临床病理参数的关系。结果胃癌组织中S100A11、MMP-9的阳性表达率显著高于癌旁正常组织(P<0.05)。胃癌组织中E-cadherin的阳性表达率显著低于癌旁正常组织(P<0.05)。胃癌组织中S100A11、MMP-9及E-cadherin的表达与临床分期、淋巴结转移及浸润深度密切相关,而与年龄、性别无关。同时胃癌组织中S100A11、MMP-9及E-cadherin表达具有相关性。结论高表达的S100A11、MMP-9及低表达的E-cadherin对胃癌的发生发展起促进作用,可能成为胃癌诊断的判断指标。 Objective To explore significance and expression of S100 calcium-binding protein A11(S100 A11),matrixmetalloproteinase-9(MMP-9) and E-cadherin in gastric cancer.Methods The expression of S100 A11,MMP-9 and E-cadherin in 92 cases of gastric cancer and 92 cases of adjacent normal tissues were detected by immunohistochemical method.The relationship between S100 A11,MMP-9,E-cadherin and clinical pathological parameters was analyzed.Results The positive rate of S100 A11 and MMP-9 in gastric cancer was higher than that in adjacent normal tissues(P < 0.05).The positive rate of S100 A11,MMP-9 and E-cadherin were closely related with clinical stage,lymph node metastasis and depth of invasion,but not with age and sex.The positive rate of S100 A11,MMP-9 and E-cadherin in gastric cancer tissues was correlated.Conclusion Higher expression of S100 A11 and MMP-9,lower expression of E-cadherin can promote the occurrence and development of gastric cancer,and can be used as markers for the diagnosis of gastric cancer.
出处 《临床和实验医学杂志》 2018年第3期268-270,共3页 Journal of Clinical and Experimental Medicine
关键词 胃癌 S100钙结合蛋白A11 基质金属蛋白酶-9 E-钙黏蛋白 Gastric cancer S100 calcium-binding protein A11 Matrixmetalloproteinase-9 E-cadherin
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  • 1陆洪炳,殷飞燕.Snail基因在不同分化程度胃癌细胞中的表达及其意义[J].实用癌症杂志,2010,25(5):457-459. 被引量:2
  • 2Chen, Jian-Hua,Ni, Run-Zhou,Xiao, Ming-Bing,Guo, Ji-Guang,Zhou, Jia-Wei.Comparative proteomic analysis of differentially expressed proteins in human pancreatic cancer tissue[J].Hepatobiliary & Pancreatic Diseases International,2009,8(2):193-200. 被引量:27
  • 3高鹏,王培戈,范晓琳,崔铮,陈咸增.Maspin和E-cadherin蛋白表达与胃癌临床病理学的关系[J].山东医药,2007,47(6):30-31. 被引量:3
  • 4Thiery JP. Epithelial mesenchymal transitions in development and pathologies[J. Current ()pinion in Cell Biology, 2003,15 (2) = 740-746.
  • 5Rosivatz E, Becket I,Specht K, et al. Differential expression of the epithelial mesenchymal transition regulators Snail, SIP1, Twist in gastric cancer[J. Am J Pathol,2002,161(9)=1881 i891.
  • 6Hirohashi S. Inactivation of the E-cadherin-mediated cell adhe- sion system in human cancerEJ. Am J Pathol, 1998,153 ( 6 ) .- 333-339.
  • 7Batlle E, Sancho E,Franci C, et al. The transcription factor snail is a repressor of E-cadherin gene expression in epithelial tumour cellsEJ. Nature Cell Biol,2000,2(5) :84-89.
  • 8Cano A, Moreno MA,Rodrigo I, et al. The transcription factor snail controls epithelial-mesenchymal transitions by repressing E-eadherin expressionJ]. Nature Cell Biol, 2000,2 ( 1), 76 83.
  • 9Batlle E, Sancho E,Franci C, et al. The transcription factor snail is a repressor of E-cadherin gene expression in epithelial tumour cellsEJ. Nature Cell Biol,2000,2(5) .-84-89.
  • 10Cano A, Moreno MA, Rodrigo I, et al. The transcription factor snail controls epithelial-mesenchymal transitions by repressing E-cadherin expression[J]. Nature Cell Biol, 2000,2 ( 1), 76 83.

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