期刊文献+

不同分化程度胃癌组织中WNT3的表达及意义 被引量:2

Expression of WNT3 in Human Gastric Carcinoma with Different Differentiation Degrees
下载PDF
导出
摘要 通过观察WNT3在不同分化程度胃癌中的表达差异及其与胃癌患者临床病理资料之间的关系,来探讨WNT3在胃癌发病过程中的作用.本研究采用Real time PCR及免疫组化的方法,对比分析了46例高分化、55例中分化、58例低分化胃癌及15例正常组织中WNT3基因在转录和翻译水平的表达情况.Real time PCR结果显示,在不同分化程度的胃癌组织中,WNT3mRNA的表达较正常对照组织显著升高,差异具有统计学意义(P<0.05).免疫组化结果显示,与正常对照组相比,高分化、中分化、低分化胃癌组织中wnt3蛋白的含量逐渐增高,不同分化程度的胃癌组织与正常组间的差异具有统计学意义(P<0.05).临床资料分析表明,wnt3在胃癌中的表达与患者的性别、年龄等无关,而与淋巴结转移有关.因此,wnt3可能是启动WNT经典信号,参与胃癌发生、发展的重要分子. The WNT3 expression in gastric carcinoma with different differentiation degrees, which from different patients,was examined to explore the roles of WNT3 in the pathogenesis of human gastric carcinoma. WNT3 transcription and translation levels were compared among 46 well, 55 moderately and 58 poorly differentiated gastric carcinoma tissues by real-time PCR and immuno- histochemistry methods. Normal gastric tissue was used as control. As revealed by real-time PCR results,WNT3 mRNA expression in different differentiated gastric carcinoma were significantly higher than control group (P〈0.05). The expression levels of wnt3 protein in different differentiated gastric carcinoma were significantly higher than in control group (P〈0.05),and the protein levels gradually increased in well, moderately and poorly differentiated tissues, respectively. Moreover,the wnt3 protein level was only affected by whether the gastric carcinoma had metastasized to the lymph node, but not the sex and age of patients. Therefore, wnt3 could be an important factor to start the WNT classic signal pathway,then take part in the gastric carcinoma genesis and development process.
出处 《内蒙古大学学报(自然科学版)》 CAS 北大核心 2015年第1期66-70,共5页 Journal of Inner Mongolia University:Natural Science Edition
基金 内蒙古自治区教育厅重点项目(NJZZ12149) 内蒙古自治区卫生厅项目(2010218) 内蒙古教育厅自然科学项目(NJZY11121)
关键词 WNT3 胃癌组织 REAL TIME PCR 免疫组织化学 WNT3 gastric carcinoma tissues real time PCR immunohistochemistry
  • 相关文献

参考文献1

二级参考文献31

  • 1[1]Pishvaian MJ,Byers SW.Biomarkers of WNT signaling.Cancer Biomark 2007;3:263-274
  • 2[2]Neth P,Ries C,Karow M,Egea V,Ilmer M,Jochum M.The Wnt signal transduction pathway in stem cells and cancer cells:influence on cellular invasion.Stem Cell Rev 2007;3:18-29
  • 3[3]Herbst A,Kolligs FT.Wnt signaling as a therapeutic target for cancer.Methods Mol Biol 2007;361:63-91
  • 4[4]Akiyama T.Wnt/beta-catenin signaling.Cytokine Growth Factor Rev 2000;11:273-282
  • 5[5]Kikuchi A.Modulation of Wnt signaling by Axin and Axil.Cytokine Growth Factor Rev 1999;10:255-265
  • 6[6]Satoh S,Daigo Y,Furukawa Y,Kato T,Miwa N,Nishiwaki T,Kawasoe T,Ishiguro H,Fujita M,Tokino T,Sasaki Y,Imaoka S,Murata M,Shimano T,Yamaoka Y,Nakamura Y.AXIN1 mutations in hepatocellular carcinomas,and growth suppression in cancer cells by virus-mediated transfer of AXIN1.Nat Genet 2000;24:245-250
  • 7[7]Liu W,Dong X,Mai M,Seelan RS,Taniguchi K,Krishnadath KK,Hailing KC,Cunningham JM,Boardman LA,Qian C,Christensen E,Schmidt SS,Roche PC,Smith DI,Thibodeau SN.Mutations in AXIN2 cause colorectal cancer with defective mismatch repair by activating beta-catenin/TCF signalling.Nat Genet 2000;26:146-147
  • 8[8]Behrens J,Jerchow BA,Wurtele M,Grimm J,Asbrand C,Wirtz R,Kuhl M,Wedlich D,Birchmeier W.Functional interaction of an axin homolog,conductin,with beta-catenin,APC,and GSK3beta.Science 1998;280:596-599
  • 9[9]Hart MJ,de los Santos R,Albert IN,Rubinfeld B,Polakis P.Downregulation of beta-catenin by human Axin and its association with the APC tumor suppressor,beta-catenin and GSK3 beta.Curr Biol 1998;8:573-581
  • 10[10]Dahmen RP,Koch A,Denkhaus D,Tonn JC,Sorensen N,Berthold F,Behrens J,Birchmeier W,Wiestler OD,Pietsch T.Deletions of AXIN1,a component of the WNT/wingless pathway,in sporadic medulloblastomas.Cancer Res 2001;61:7039-7043

共引文献10

同被引文献9

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