期刊文献+

结直肠癌组织中Pin1和β-catenin的表达及其预后意义

Pin1 overexpression in colorectal cancer and its correlation with β-catenin
下载PDF
导出
摘要 目的:探讨肽基脯氨酰顺反异构酶Pin1与β-联蛋白(β-catenin)在结直肠癌组织中的表达及其预后关系。方法:应用免疫组化技术检测结直肠癌组织中Pin1、β-catenin蛋白表达水平,分析其相互关系及其预后价值。所有统计分析采用SPSS11.5软件包完成。结果:①Pin1在40%(12/30)结直肠癌组织中过表达,β-catenin在60%(18/30)结直肠癌组织中异常蓄积,12例Pin1过表达中11例同时存在β-catenin异常蓄积,两者呈显著正相关(P=0.008);②统计分析提示Pin1过表达与预后有显著相关性(P<0.01),β-catenin与预后关系无显著统计学意义(P=0.092)。结论:结直肠癌组织中存在Pin1过表达、β-catenin异常蓄积,且两者正相关;Pin1与结直肠癌的预后密切相关。 Objective:To evaluate the expression of Pin1 and β-catenin in colorectal cancer.To identify whether Pin1 was a prognostic factor in colorectal cancer.Methods:The expression of Pin1 and β-catenin proteins was detected by immunohistochemistry in 30 cases of colorectal cancer tissues.The relationships between Pin1 and β-catenin expression and their prognostic factors were evaluated.Results:1.The overexpression of Pin1 and the aberrant accumulation of β-catenin in colorectal cancer were 38%(12/30) and 60%(18/30), respectively.A significant positive correlation was found between Pin1 and β-catenin(p=0.008).2.Pin1 was significantly related to the overall survival(p<0.01).Patients with negative β-catenin expression survived longer than those with aberrant expression despite no statistical significance was detected(p=0.092).Conclusion:Pin1 was overexpressed and β-catenin was aberrant accumulated in colorectal cancer in this study.There was a significant correlation between their expressions.Pin1 might be a prognostic factor in colorectal cancer.
出处 《内蒙古中医药》 2008年第12X期43-45,共3页 Inner Mongolia Journal of Traditional Chinese Medicine
关键词 PIN1 Β-CATENIN 结直肠癌 免疫组织化学 pin1 β-catenin colorectal cancer immunohistochemistry
  • 相关文献

参考文献10

  • 1Lin,S.Y.et al.β-Catenin,a novel prognostic marker for breast cancer:its roles in cyclin D1expression and cancer pro-gression[].Proceedings of the National Academy of Sciences of the United States of America. 被引量:1
  • 2Maruyama K,Ochiai A,Akimoto S,et al.Cytoplasmic beta-catenin accumulation as a predictor of hematogenous metastasis in human colorectal cancer[].Oncology.2000 被引量:1
  • 3Yaffe MB,Schutkowski M,Shen M,et al.Sequence-specific and phosphorylation-dependent proline isomerization:a potential mitotic regulatory mechanism[].Science.1997 被引量:1
  • 4LU K P,HANES S D,HUNTER T.A human peptidyl prolyl isomerase essential for regulation of mitosis[].Nature.1996 被引量:1
  • 5Ryo A,Liou Y C,Lu K P et al.Prolyl isomerase Pin1: a catalyst for oncogenesis and a potential therapeutic target in cancer[].Journal of Cell Science.2003 被引量:1
  • 6Winkler KE,Swenson KI,Kornbluth S , et al.Requirement of the prolyl isomerase Pinl for the replication checkpoint[].Science.2000 被引量:1
  • 7LU K P.Prolyl isomerase Pin1 as a molecular target for cancer diagnostics and therapeutics[].Cancer Cell.2003 被引量:1
  • 8Bao L,Kimzey A,Sauter G,et al.Prevalent overexpression of prolyl isomerase Pin1in human cancers[].American Journal of Pathology.2004 被引量:1
  • 9Ryo A,Nakamura M,Wulf G et al.Pin1 regulates turn- over and subcellular localization of beta-catenin by inhib- iting its interaction with APC[].Nature Cell Biology.2001 被引量:1
  • 10Junichi kuramochi,Takehiro Arai,Satoshi Ikeda, et al.High Pin1 expression is associated with tumor progression in colorectal cancer[].Journal of Surgical Oncology.2006 被引量:1

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