期刊文献+

P_(53)与β-catenin在胃息肉与胃癌中的表达及相互关系 被引量:2

The Correlation of P_(53) and β-catenin Expression in Gastric Polyp and Gastric Carcinoma
下载PDF
导出
摘要 目的探讨P53与β-catenin在胃息肉和胃癌中的表达及相互关系。方法采用免疫组化法检测正常胃黏膜组、不同病理类型的胃息肉组和胃癌组中P53蛋白与β-catenin蛋白的表达情况。结果(1)P53蛋白的阳性率:胃癌组明显高于正常胃黏膜组和不同类型的胃息肉组(P<0.05);正常胃黏膜组和不同类型的胃息肉组间差异,均不具有统计学意义(P>0.05)。β-catenin蛋白的阳性率:胃癌组和不同类型的胃息肉组明显高于正常胃黏膜组(P<0.05);胃癌组和不同类型的胃息肉组间差异,均不具有统计学意义(P>0.05)。(2)β-catenin蛋白的强阳性率:胃癌组明显高于不同类型的胃息肉组,差异均具有统计学意义(P<0.05)。结论在胃息肉阶段抑癌基因P53保持相对正常的结构和功能,癌基因β-catenin表达增强,增强的程度明显低于胃癌阶段。 Objective To discuss the correlation of P53 and β-catenin expression in gastric polyp and gastric carcinoma.Methods The expression of P53 protein andβ-catenin protein were examined using immunohistochemical staining in normal gastric mucosa group(group A) and different pathologic types of gastric polyps group(group B) and gastric carcinoma group(group C).Results The positive rates of P53 protein in group C were obviously higher than that in group A and group B(P〈0.05).Between the group A and group B,there were no significant differences in the positive rates of P53 protein(P〉0.05).The positive rates of β-catenin protein in group C and group B were obviously higher than that in group A(P〈0.05).Between the group C and group B,there were no significant differences(P〉0.05).The strong positive rates of β-catenin protein in group C were higher than that in group B(P〈0.05).Conclusion Tumor suppressor gene P53 keeps relatively normal construction and function in gastric polyp,however,the expression of oncogene β-catenin in gastric carcinoma were higher than in gastric polyp.
出处 《黑龙江医学》 2010年第2期93-95,共3页 Heilongjiang Medical Journal
关键词 P53 Β-CATENIN 胃息肉 胃癌 P53 β-catenin Gastric Polyp Gastric Carcinoma
  • 相关文献

参考文献13

  • 1Landis S H,Murray T,Bolden S,et al.Cancer Statistics[J].CA Cancer JClin,1999,49:8. 被引量:1
  • 2E Tahara.Genetic pathways of two types ofgastric cancer[J].IARC SciPub,1 2004,(157):327-349. 被引量:1
  • 3Finlay C A,Hinds P W,Levine A J.The P53 proto-oncogene can act as a suppressor of transformation[J].Cell,1989,57(7):1 083-1 093. 被引量:1
  • 4朱志兵,薛英威,庞达.p53在胃癌分子生物学研究中的进展[J].实用肿瘤学杂志,2001,15(4):317-319. 被引量:3
  • 5Lim S C,Lee M S.Significance orE-cadhefin/β-catenin com-plex and cyclin Dl in breast cancer[J].Oncol Rep,2002,9(5):915-928. 被引量:1
  • 6徐洪涛,王恩华.E钙粘蛋白-环连蛋白复合体与肿瘤[J].国外医学(肿瘤学分册),2004,31(2):107-110. 被引量:16
  • 7Pennisi E.How a growth control path takes awrong turn to cancer[J].Science,1998,281(5 382):1 438-1 441. 被引量:1
  • 8NakashimaM,Meirmanov S,NarukeY,et al.CyclinDl overex-pression in thyroid tumours from a radio-contaminated area and its correlation with Pinl and aberrantβ-catenin expression[J].J Patho,2004,202(4):446-455. 被引量:1
  • 9Song B J,ParkY J,Kim H S,et al.Expression ofbeta-catenin and E-cadhefin in early gastric cancer:correlation with clinico-pathologic parameters[J].Korea J Gastroentero,2004,43(2):82-89. 被引量:1
  • 10Rask K,Nilsson A,Brannstrom M,et al.Wnt-signalling pathway in ovarian epithelial tumors:increased expression of beta-catenin and GSK3β[J].Br J Cancer,2003,89(7):298-304. 被引量:1

二级参考文献31

共引文献1389

同被引文献2

引证文献2

二级引证文献2

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