期刊文献+

c-Jun、Smad7蛋白在大肠腺癌中的表达及临床意义

The expression and clinical significance of c-Jun and Smad7 proteins in colorectal adenocarcinoma
下载PDF
导出
摘要 目的探讨c-Jun、Smad7蛋白在大肠癌中的表达及其对肿瘤发生、发展的影响。方法采用免疫组化方法,分别检测20例正常大肠黏膜、20例大肠腺瘤及65例大肠腺癌中c-Jun、Smad7蛋白表达水平,比较两种蛋白的表达情况。结果 c-Jun蛋白在大肠腺癌组织中的表达率为72.30%,与正常对照组比较差异有统计学意义(P<0.05);高分化腺癌与中-低分化腺癌相比,差异有统计学意义(P<0.05);TNMⅢ+Ⅳ期表达率显著低于Ⅰ+Ⅱ期(P<0.05);Smad7蛋白在大肠腺癌组织中的表达率为89.23%,与对照组比较差异有统计学意义(P<0.05);中-低分化者、有淋巴结转移者与高分化者、无淋巴结转移者比较差异均有统计学意义(P均<0.05)。c-Jun蛋白与Smad7蛋白在大肠腺癌中的表达水平呈正相关(P<0.05,r s=0.3460)。结论 c-Jun、Smad7蛋白在大肠腺癌的发生、发展整个过程的不同阶段具有促进作用,对于临床诊断大肠癌及判断病情、预后有重要意义。 Objective To study the expression of c-Jun, Smad7 proteins and the effect on colorectal adenocarcino- ma. Methods The expression of c-Jun, Smad7 proteins were detected by the immunohistochemical (IHC) staining technique in colorectal adenocarcinoma (65 cases) , normal colorectal mucosa (20 cases) and colorctal adenoma (20 cases) , the expression of two proteins were compared, respectively. Results The expression of c-Jun protein in color- ectal adenocarcinoma tissues was 72.30% , and had statistical significance compared with the normal control group ( P 〈 0.05). There was significant difference between well-differentiated and poorly differentiated colorectal adenocarcinoma (P 〈 0.05). The expression of c-Jun in TNM m + rv was significantly lower than that of TNM I + II (P 〈 0.05). The expression of Smad7 protein was 89.23% and had statistically significant compared with normal control group (P 〈 O. 05). Meanwhile the Smad7 protein in patients with poorly differentiated and with lymph node metastasis was higher than that in patients with well-differentiated and without lymph node metastasis (P 〈 0.05). There was a postive corre- lation between c-Jun protein and Smad7 protein in colorectal adenocarcinoma (P 〈 0.05, r, = 0. 3460). Conclusion The c-Jun and Smad7 proteins could promote the development of colorectal adenocarcinoma and could be play important roles in clinical diagnosis and prognosis.
出处 《胃肠病学和肝病学杂志》 CAS 2014年第1期36-38,共3页 Chinese Journal of Gastroenterology and Hepatology
基金 安徽宿州市科技局基金资助项目(NO201025)
关键词 大肠腺癌 C-JUN SMAD7 免疫组织化学 Colorectal adenocarcinoma C-Jun Smad7 Immunohistochemistry
  • 相关文献

参考文献6

二级参考文献56

  • 1许光兰,梁劲松,以敏,陈平,黄小琪,何胜东.青蒿琥酯对肺纤维化大鼠肺组织转化生长因子β1的影响[J].广西医学院学报,2008,18(3):400-403. 被引量:6
  • 2申洪.免疫组织化学染色定量方法研究(Ⅲ)[J].中国组织化学与细胞化学杂志,1995,4(1):89-92. 被引量:398
  • 3王莉,霍艳英,张开泰,王莹,项晓琼,胡迎春,余刚,李刚,米粲,吴德昌.BEP2D细胞恶性转化过程中Smad7基因对MAPK信号通路的调控[J].癌症,2005,24(9):1080-1084. 被引量:10
  • 4Han G, Lu SL, Li AG, et al. Distinct mechanisms of TGF-beta1-mediated epithelial-to-mesenchymal transition and metastasis during skin carcinogenesis[J]. J Clin Invest, 2005,115(7):1714-1723. 被引量:1
  • 5Krakowski AR, Laboureau J, Mauviel A, et al. Cytoplasmic SnoN in normal tissues and nonmalignant cells antagonizes TGF-beta signaling by sequestration of the Smad proteins[J]. Proc Natl Acad Sci USA, 2005,102(35):12437-12442. 被引量:1
  • 6Munoz O, Fend F, De Beaumont R, et al. TGF-beta-mediated activation of Smad1 in B-cell non-Hodgkin's lymphoma and effect on cell proliferation[J]. Leukemia, 2004,18(12):2015-2025. 被引量:1
  • 7Bachmeier BE, Ruoss I, Hagedorn HG, et al. Molecular analysis of TGFβs and their receptors in human keratinocyte cell lines of different biological behaviour[J]. Int J Mol Med, 2002,10(4):371-376. 被引量:1
  • 8Hagedorn HG, Bachmeier BE, Nerlich AG. Synthesis and degradation of basement membranes and extracellular matrix and their regulation by TGF-beta in invasive carcinomas[J]. Int J Oncol, 2001,18(4):669-681. 被引量:1
  • 9Halder SK, Beauchamp RD, Datta PK. Smad7 induces tumorigenicity by blocking TGF-beta-induced growth inhibition and apoptosis[J]. Exp Cell Res, 2005,307(1):231-246. 被引量:1
  • 10Kleeff J, Ishiwata T, Maruyama H, et al. The TGF beta signaling inhibitor Smad7 enhances tumorigenicity in pancreatic cancer[J]. Oncogene, 1999,18(39):5363-5372. 被引量:1

共引文献32

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