期刊文献+

E-cad在肺癌的表达及意义

Expression and significance of E-cadherin in lung carcinoma
下载PDF
导出
摘要 目的研究E-cad在肺癌的表达及意义,探讨其与肺癌的组织类型、病理分级及淋巴结转移的关系。方法应用免疫组化S-P法检测E-cad在104例肺癌的表达,其中鳞癌46例、腺癌33例、小细胞癌10例、其它类型癌15例。结果E-cad在104例肺癌的阳性表达为鳞癌21例(45.7%),腺癌14例(42.4%),小细胞癌5例(50%),其它类型癌为7例(46.7%)。结果显示E-cad的阳性表达与肺癌组织类型无相关性(P>0.05);淋巴结转移阳性表达(32.1%),无淋巴结转移阳性表达(64.6%),二者表达有显著相关性(P<0.05);病理分级(腺癌、鳞癌)Ⅰ级阳性表达(55.6%),Ⅱ级阳性表达(40%),Ⅲ级阳性表达(29.6%),结果显示也有明显相关性(P<0.05)。结论肺癌组织中E-cad的阳性表达与肺癌淋巴结转移及分化程度有关。检测E-cad的表达可作为判断肺癌预后的重要指标。 Objective To study the expression and significance of E-cadherin in lung carcinoma. Methods The expression of E-cadherin was studied by immunohistochemical technique (S-P method) in 104 cases of lung carcinoma (15 cases of squamous cell carcinomas,33 cases of adenocarcinomas,10 cases of small- cell carcinomas,15 cases of other carcinomas).Results Positive expression of E-cadherin was detected in 21 of 46 cases of squamous cell carcinomas (45.7%),in 14 of 33 cases of adenocarcinomas (42.4%),in 5 of 10 cases of small carcinomas (50%) and in 7 of 15 cases of other carcinomas (46.7%).E-cadherin exprression rate of well differentiated carcinoma and moderately differentiated carcinoma was significant higher than that of poorly differentiated carcinoma (P<0.05).The expression rate of E-cadherin in lung carcinoma without lymph node metastasis was significant highetr than those with lympy node metastasis(P<0.05).Conclusion The expression of E-cadherin can be regarded as valuable indicators for evaluating biological behavior and the prognosis of lung carcinoma.
作者 曾绍文
机构地区 汕头市中心医院
出处 《基层医学论坛》 2005年第3期194-195,共2页 The Medical Forum
关键词 阳性表达 E—cad 肺癌 淋巴结转移 鳞癌 腺癌 E-CAD 类型 结论 意义 Lung neoplasms Cadherins Immunohistochemistry
  • 相关文献

参考文献2

二级参考文献15

  • 1Shibamoto S, Hayakawa M, Takeuchik, et al.Tyrosin phosphorylation if betacatenin and plakoglokin enhanced by hepatocyet growth factor and epidermal growth factor in human carcinoma cells. Cell Adhesion Commun, 1994,4:295-305.
  • 2Rubinfeld B, Souza B, Albert B,et al.The APC protein and E-cadberin form similar, beta-catenin, and plakoglobin. J Biol Chem,1995,270:5549-5555.
  • 3Jang WG, Puntis MCA, Hallett AB. Molecular and cellular basis of treatment. Br J Surg, 1994,81:1576-1590.
  • 4Behrens J.Cadherins and deldrminants of tissue morphology and suppresion of invasion.Anat, 1994,149:165-169.
  • 5Shiozaki,Oka H,Lnoue M,et al.E-cadherin mediated adhesion system in cancer cells.Cancer, 1996,77:1605-1613.
  • 6Hanby AM,Chinery R, Poulsom R,et al.Downregulation of E-cadherin in the reparative epithelium of the human gastrointestinal tract.Am J Patol, 1996,148:723-729.
  • 7Vessey CJ,Wilding J,Folarin LV,et al.Altered expression and function of E-cadherin in cervical intraepithelial neoplasia and invasive squamous cell carcinoma.J Pathol,1995,176:151-1593.
  • 8Jones JL,Royell JE,Walker RA.E-cadherin relates to EGFR expression and lymph node metatasis in primary breast carcinoma.Br J Cancer,1996,74:1237-1241.
  • 9Bongiorno PF,AL-Kasspooles M,Lee SW,et al.E-cadherin expression in primary and metastatic thoratic neoplasmas and in barrent's oesophagns.Br J Cancer, 1995,71:166-172.
  • 10Nathre I, Hink L, Swedlow JR, et al, Defining interactions and distributions of cadherin and catenin complexes in polarizedepithelial cells, J cell Biol 1994,125:1341-1352.

共引文献19

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