期刊文献+

Wnt3、Wnt3a在胃癌组织中的表达及意义 被引量:15

Significance of expression of Wnt3 and Wnt3a in gastric carcinoma
下载PDF
导出
摘要 目的:探讨Wnt3、Wnt3a、Wnt5a、Wnt8a和β-catenin基因在胃癌及慢性萎缩性胃炎(chronic atrophic gastritis,CAG)组织中的表达及在胃癌发生、发展中的作用.方法:应用Real-time RT-PCR方法检测26例CAG和40例胃癌组织中Wnt3、Wnt3a、Wnt5a、Wnt8a mRNA的表达情况,Westernblot检测β-catenin蛋白的表达.结果:Wnt3和Wnt3a mRNA的表达在胃癌组织中较CAG中升高(1.9940±0.1311vs1.3349±0.2487,P<0.05;2.3033±0.3979vs1.2835±0.2815,P<0.05),并与胃癌的淋巴结转移及TNM分期具有相关性,而Wnt5a和Wnt8a在两种组织中的表达无显著差异(P>0.05),Western blot结果显示β-catenin蛋白在胃癌中表达升高(0.6290±0.1369,0.2341±0.0975,P<0.05).结论:Wnt/β-catenin信号通路在胃癌组织中呈活化状态,而Wnt3和Wnt3a可能在启动此通路的激活过程中起到了主要作用,并参与了胃癌的发生发展. AIM: To detect the expression of Wnt3, Wnt3a, Wnt5a, Wnt8a andβ-catenin in chronic atrophic gastritis (CAG) and gastric carcinoma (GC), and to investigate the role of the Wnt signaling path- way in the pathogenesis of GC. METHODS: The mRNA expression of Wnt3, Wnt3a, Wnt5a and Wnt8a in 26 fresh CAG and 40 GC tissue samples was examined using Real-time RT-PCR. The protein expression of β-catenin was detected by Western blot RESULTS: The mRNA expression levels of Wnt3 and Wnt3a were significantly increased in GC (1.9940 ±0.1311 vs 1.3349 ±0.2487, P 〈 0.05; 2.3033± 0.3979 vs 1.2835 ± 0.2815, P 〈 0.05) and were associated with lymph node metastasis and TNM stage. The expression of Wnt5a and Wnt8a did not significantly differ between CAG and GC (both P 〉 0.05). Western blot analysis showed that the relative expression of β-catenin protein was significantly elevated in GC com- pared with CAG (0.6290 ± 0.1369 vs 0.2341± 0.0975, P 〈 0.05). CONCLUSION: Our results suggest that Wnt3 and Wnt3a may be critically involved in the acti- vation of the Wnt signaling pathway and in the carcinogenesis and progression of GC.
出处 《世界华人消化杂志》 CAS 北大核心 2013年第7期624-628,共5页 World Chinese Journal of Digestology
基金 山东省自然科学基金资助项目 No.ZR2009CQ040~~
关键词 慢性萎缩性胃炎 胃癌 Β-CATENIN WNT信号通路 基因表达 Key Words: Chronic atrophic gastritis Gastric can-cer β-catenin Wnt signaling pathway Gene ex-pression
  • 相关文献

参考文献3

二级参考文献72

  • 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21

同被引文献144

引证文献15

二级引证文献79

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