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NDRG1及nm23蛋白在大肠腺癌中的表达及其相互关系

Correlation and Expression of NDRG1 and nm23 in Colorectal Adenocarcinomas
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摘要 目的研究NDRG1、nm23蛋白在大肠腺癌淋巴结转移中的作用,并探讨二者在大肠腺癌淋巴结转移中的相互关系.方法采用免疫组化方法,观察无淋巴结转移的大肠腺癌、有淋巴结转移的大肠腺癌中NDRG1蛋白及nm23蛋白表达特点.结果NDRG1蛋白表达与大肠腺癌有无淋巴结转移差异有统计学意义(P<0.05),且呈正相关关系(P<0.05).nm23蛋白表达与大肠腺癌有无淋巴结转移差异有统计学意义(P<0.05),但呈负相关关系(P<0.05).无淋巴结转移的大肠腺癌及有淋巴结转移的大肠腺癌中NDRG1蛋白与nm23蛋白表达之间均未见相关性(P>0.05).结论NDRG1蛋白与nm23蛋白可能在大肠腺癌淋巴结转移的不同环节发挥作用. Objective To study the correlations and functions of NDRG1 and nm23 protein in the metastases of colorectal adenocarcinoma. Methods NDRG1 and nm23 were detected at their protein levels by immunohistochemical (IHC) staining technique in colorectal carcinomas with no regional lymph nodes metastasis and colorectal carcinomas with regional lymph nodes metastasis. Results There was significant difference between the expressions of NDRG1 in colorectal carcinomas with no regional lymph nodes metastasis and those with regional lymph nodes metastasis, and the correlation was positive (P 〈 0.05). Most carcinomas with regional lymph nodes metastasis showed reduced nm23 expression, as compared to the carcinomas with no regional lymph nodes metastasis, and the correlation was negative (P 〈 0.05). There was no obvious correlation between the expressions of NDRG1 and the expressions of nm23. Conclusion NDRG1 protein and nm23 protein may play different roles respectively in the different processes of colorectal carcinomas metastasis.
出处 《昆明医学院学报》 2008年第3期28-31,共4页 Journal of Kunming Medical College
关键词 大肠肿瘤 转移 NDRG1蛋白 NM23蛋白 免疫组化 Colorectal neoplasm Metastasis NDRG1 nm23 Immunohistochemistry
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  • 1Sinicrope F A,Cancer Res,1995年,55卷,2期,237页
  • 2Melnyk O, Shuman MA, Kim KJ. Vascular endothelial growth fac tor promotes tumor d issemination by a mechanism distinct from its effect on primary tumor growth. C ancer Res, 1996,56:921-925.
  • 3Van der Wurrf A, Vermeulen SJ, Van der Linden EP,et al. Patterns of α- and β-catenin and E-cadherin expression in colorectal adenomas and carcinomas. J P athol, 1997,182:325-330.
  • 4Junji G, Hitoshi S, Toshimasa T, et al. Expressioin of E-cadherin and α-cat e nin in patients with colorectal cancer. Correlation with cancer invasion and me tastasis. Am J Clin Pathol, 1999,111:29-42.
  • 5Goi T, Yamaguchi A, Nakagawara G, et al. Reduced expression of deleted color e ctal carcinoma(DDC) protein in established colon cancers. Br J Cancer, 1998,77 :466.
  • 6Matsumura Y, Hanbury D, Smith J, et al. Non-invasive detection of malignancy by identification of unusual CD44 gene activity in exfoliated cancer cells. BMJ , 1998,308:619-624.
  • 7Ropponen K, Tammi M, Parkinen J, et al. Tumor-cell-associated hyaluronan as a n unfavorable prognostic factor in colorectal cancer. Cancer Res, 1998,58:342- 347.
  • 8Hideki M, Hisaguki A. Host expreesion of matrix metalloproteinase-2 and tiss u e inhibitor of metalloproteinase-2 in normal colon tissue affects metastatic pot ential of colorectal cancer. Dis colon Rectum, 1998,42:383-402.
  • 9Liabakk NB, Talbot I, Smith RA, et al. Matrix metalloproteinase-2(MMP-2) and matrix metalloproteinase-9(MMP-9) type Ⅳ collagenase in colorectal cancer. Can cer Res, 1996,56:190-206.
  • 10Marray GI, Duncan ME, O'Neil P. MMP-1 is associated with poor prognosis in c olorectal cancer. Nat Med, 1996,2:461-2462.

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