期刊文献+

EMMPRIN和MMP-2的表达与大肠癌临床病理学的关系及意义 被引量:5

Corrlations of EMMPRIN and MMP-2 expressions with clinicopathological features in colon cancer
在线阅读 下载PDF
导出
摘要 目的:探讨大肠癌组织EMMPRIN和MMP-2蛋白的表达意义.方法:大肠癌患者108例,以正常结、大肠黏膜30例作为对照,应用SABC免疫组化方法检测EMMPRIN和MMP-2蛋白的表达.结果:大肠癌组织EMMPRIN和MMP2蛋白的阳性表达率分别为81.5%(88/108)和86.1%(93/108),明显高于正常大肠黏膜组织(6.7%和20.0%,P<0.01).EMMPRIN和MMP2在中、低分化癌中的强阳性表达率高于高分化癌(P<0.05);浆膜浸润及淋巴结转移组的强阳性率高于无浸润及淋巴结转移组(P<0.01);Dukes C^D期的强阳性表达率高于Dukes A^B期(P<0.01).EMM-PRIN和MMP2的表达一致率为91.4%(85/93),Spearman等级相关性检验分析表明大肠癌组织中EMMPRIN的表达和MMP2的表达之间呈正相关(r=0.608,P<0.01).结论:EMMPRIN和MMP-2与大肠癌的发生、浸润、转移有关,可作为新的大肠癌标记物用于联合检测,具有重要的临床意义. AIM: To analyze the expressions of EMMPRIN and MMP-2 in human colon cancer, and to evaluate the clinical significance of these two markers in the progression of colon cancer. METHODS: One hundred and eight patients with colon cancer were examined for the expressions of EMMPRIN and MMP-2 by SABC immunohistochemistry, and compared with 30 control cases of normal colon tissue. RESULTS : The positive expression rates of EMMPRIN and MMP2 in 108 patients with the cancer of colon were 81.5% (88/108) and 86.1% (93/108) respectively, which were significantly higher than those in 30 cases of normal colorectal mucosa( 6. 67% and 20.0% , P 〈0.01 ). The expressions of EMMPRIN and MMP2 in moderately-poorly differentiated cancer of colon increased dramatically compared with those in well differentiated tissues ( P 〈 0.05 ) , and the positivity rates of EMMPRIN and MMP2 in tumor tissues with ectoptygma invasion and lymph node metastasis were higher than those without them( P 〈 0.01 ). Among Dukes staging, the positivity rates of EMMPRIN and MMP2 in the stages of C-D were higher than those in A-B ( P 〈 0.01 ). The expression rate of EMMPRIN was positively correlated with the expression of MMP2 in the cancer of colon ( r = 0. 608, P 〈0.01 ). CONCLUSION: The expressions of EMMPRIN or MMP-2 may be important features of cancer of colon. A combined detection of them may benefit us in prediction of the progression of cancer of colon.
出处 《第四军医大学学报》 北大核心 2008年第14期1319-1321,共3页 Journal of the Fourth Military Medical University
关键词 EMMPRIN 明胶酶A 结肠肿瘤 病理学 临床 EMMPRIN gelatinase A colonic neoplasms pathology, clinical
  • 相关文献

参考文献9

  • 1刘鹏飞,唐文渊,朱政鸣.CD147和MMP-2、MMP-9与胶质细胞瘤侵袭性的关系[J].重庆医学,2005,34(11):1736-1739. 被引量:3
  • 2蒋建利,姚西英,周筠,黄勇,张阳,陈志南.HAb18G/CD147刺激人肝癌细胞分泌基质金属蛋白酶的机制探讨[J].肿瘤,2004,24(6):534-537. 被引量:9
  • 3周晟,刘聪,吴时敏,吴人亮.CD147和MMP-2在乳腺癌组织中的表达及其与预后的相关性[J].癌症,2005,24(7):874-879. 被引量:14
  • 4黄灵芝,王字玲.CD147的研究进展[J].生物技术通讯,2007,18(3):472-475. 被引量:8
  • 5Jin OS,Hsieh DS,Lin YF, et al. Increasing expression of extraeellular matrix metalloprotease inducer in renal cell carcinoma: tissue microarray analysis of immunostaining score with clinicopathologlcal parameters[ J]. Int J Urol,2006,13:573 -580.
  • 6Zhang WW, Erkan M, Abiatari I, et al. Expression of extracellular matrix metalloproteinase inducer(EMMPRIN/CD147) in pancreatic neoplasm and pancreatic stellate cells[ J]. Cancer Biol Ther,2007, 6:2, e1-e10.
  • 7Reimers N,Zafrakas K,Assmann V, et al. Expression of extracellular matrix metalloproteases inducer on micrometastatic and primary mammary carcinoma cells [ J ]. Clin Cancer Res, 2004, 10: 3422 - 3428.
  • 8Nabeshima K, Suzumiya J, Nagano M, et al. Emmprin, a cell surface inducer of matrix metalloproteinases(mmps) , is expressed in tcell lymphomas[ J]. J Pathol,2004,202:341 - 351.
  • 9Sheu BC, Lien HC, Ho HN, et al. Increased expression and activation of gelatinolytic matrix metalloproteinases is associated with the progression and recurrence of human cervical cancer [ J ]. Cancer Res ,2003,63:6537 - 6542.

二级参考文献94

  • 1蒋建利,姚西英,周筠,黄勇,张阳,陈志南.HAb18G/CD147刺激人肝癌细胞分泌基质金属蛋白酶的机制探讨[J].肿瘤,2004,24(6):534-537. 被引量:9
  • 2Biswas C, Zhang Y, DeCastro R, et al. The human tumor cell-derived collagenase stimulatory factor (renamed EMMPRIN) is a member of the immunoglobulin superfamily [J].Cancer Res, 1995, 55 (2): 434
  • 3Guo H, Li R, Zucker S, et al. EMMPRIN (CD147), an inducer of matrix metalloproteinase synthesis, also binds interstitial collagenase to the tumor cell surface [J]. Cancer Res,2000, 60 (4) : 888
  • 4Munshi HG, Wu YI, Ariztia EV, et al. Calcium regulation of matrix metalloproteinase-mediated migration in oral squamous cell carcinoma cells [J]. J Biol Chem, 2002, 277 (44) :41480
  • 5Jiang JL, Zhou Q, Yu MK, et al. The involvement of HAb18G/CD147 in regulation of store-operated calcium entry and metastasis of human hepatoma cells [J]. J Biol Chem,2001, 276 (50): 46870
  • 6Jiang JL, Yu MK, Chen ZN, et al. cGMP-regulated storeoperated calcium entry in human hepatoma cells [J]. Cell Biol Int, 2001, 25 (10) : 993
  • 7Lim M, Martinez T, Jablons D, et al. Tumor-derived EMMPRIN (extracellular matrix metalloproteinase inducer) stimulates collagenase transcription through MAPK p38 [J].FEBS Lett, 1998, 441 (1): 88
  • 8Lambert CA, Colige AC, Munaut C, et al. Distinct pathways in the over-expression of matrix metalloproteinases in human fibroblasts by relaxation of mechanical tension [J].Matrix Biol, 2001, 20 (7) : 397
  • 9Yao J, Xiong S, Klos K, et al. Multiple signaling pathways involved in activation of matrix metalloproteinase-9 (MMP-9)by heregulin-beta1 in human breast cancer cells [J]. Oncogene, 2001, 20 (56): 8066
  • 10Vincenti MP, Coon CI, White LA, et al. src-related tyrosine kinases regulate transcriptional activation of the interstitial collagenase gene, MMP-1, in interleukin-1-stimulated synovial fibroblasts [J]. Arthritis Rheum, 1996, 39 (4): 574

共引文献27

同被引文献31

引证文献5

二级引证文献14

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