期刊文献+

基质金属蛋白酶MMP20与喉癌的浸润和转移 被引量:2

Matrix mettallo-proteinase 20 in laryngeal squamous cell carcinoma
下载PDF
导出
摘要 目的探讨基质金属蛋白酶MMP20与喉癌浸润和转移的关系。方法用RT-PCR和免疫组化的方法,研究MMP20在喉癌组织和其相邻的正常黏膜组织的差异表达量,分析其表达与喉癌浸润和转移的关系。数据分析借助SPSS10.0软件完成。结果36例配对标本中MMP20基因在31例喉癌组织中的表达与其相应的正常黏膜组织差异表达不明显,而在5例喉癌组织中差异表达明显;MMP20蛋白绝大多数在癌巢细胞浆内表达(占93.2%,68/73),少数主要在细胞核内表达(占6.8%,5/73),MMP20蛋白在大多数喉癌组织中的表达明显高于其相应的正常黏膜组织;有淋巴结转移病例中,MMP20蛋白表达差异明显的病例数高于没有淋巴结转移者(P=0.023);5例MMP20蛋白喉癌组织细胞核内表达中有4例与淋巴结转移有关。结论MMP20蛋白在喉癌的淋巴结转移中起着重要的作用;MMP20蛋白的过度表达可作为喉癌淋巴结转移的标志。 OBJECTIVE To investigate the role of expression of matrix mettalloproteinase 20(MMP20) in invasion and metastasis of the laryngeal carcinoma. METHODS The gene expression MMP20 in fresh laryngeal cancer tissues and their corresponding normal mucosa was detected by Reverse transcriptionpolymerase chain reaction (RT-PCR). The expression of MMP20 protein in paraffin-embedded tissues was determined by immunohistochemical method. All statistical analyses were carried out with SPSS version 10.0. RESULTS In the 36 matched specimens,MMP20 gene expression was much higher in tumor tissues than that in corresponding normal tissues in 5 cases,whereas in other 31 cases,no significant difference was observed between the cancer tissues and the corresponding normal tissues. MMP20 protein was located predominantly in the tumor cell cytoplasm in most cases,in nucleus in a few cases. MMP20 protein was over-expressed in most of the laryngeal cancer tissues. In contrast, there was weakly or not expressed in corresponding normal tissues. A significant correlation was found between MMP20 protein expression and lymph node metastases(P=0.023). Four of 5 cases of MMP20 protein expressed in nucleus were related to the invasion and metastasis of laryngeal carcinomas.CONCLUSION The protein MMP20 may play a role in laryngeal cancer invasion in a certain extent,but may play an important role in lymph node metastasis of laryngeal cancer. The over-expression of MMP20 protein may be a marker for lymph node metastasis oflaryngeal cancer.
出处 《中国耳鼻咽喉头颈外科》 北大核心 2006年第7期471-474,共4页 Chinese Archives of Otolaryngology-Head and Neck Surgery
基金 国家自然科学基金资助(30170519) 安徽省教育厅自然科学基金资助(2004KJ214)
关键词 喉肿瘤 鳞状细胞 预后 基质金属蛋白酶类 生物学现象 Laryngeal Neoplasms Carcinoma, Squamous Cell Prognosis Matrix Metalloproteinases Biological Phenomena
  • 相关文献

参考文献4

二级参考文献34

  • 1唐平章,祁永发,屠规益,李庆宏,贺永东.胸大肌肌皮瓣的适应证及并发症─—379例次经验总结[J].耳鼻咽喉(头颈外科),1994,1(1):44-47. 被引量:36
  • 2唐平章,吴雪溪,祁永发.颈内动脉回流压测定用于颈总动脉结扎的危险度估计[J].耳鼻咽喉(头颈外科),1995,2(3):191-191. 被引量:5
  • 3[1]Curran S, Murray GI. Matrix metalloproteinases: molecular aspects of their role in tumor invasion and metastasis. Eur J Cancer 2000;36:1621-30.
  • 4[2]Vihinen P, Kahari VM. Matrix metalloproteinases in cancer: prognostic markers and therapeutic targets. Int J Cancer 2002;99:157-66.
  • 5[3]Yana I, Seiki M. MT-MMPs play pivotal roles in cancer dissemination. Clin Exp Metastasis 2002;19:209-15.
  • 6[4]Lang R, Braun M, Sounni NE, et al. Crystal structure of the catalytic domain of MMP-16/MT3-MMP: characterization of MT-MMP specific features. J Mol Biol 2004;336:213-25.
  • 7[5]Jiang A, Pei D. Distinct roles of catalytic and pexin-like domains in membrane-type matrix metalloproteinase (MMP)-mediated proMMP-2 activation and collagenolysis. J Biol Chem 2003;278:38765-71.
  • 8[6]Ueno H, Nakamura H, Inoue M, et al. Expression and tissue localization of membrane-types 1, 2, and 3 matrix metalloproteinases in human invasive breast carcinomas. Cancer Res 1997;57:2055-60.
  • 9[7]Nakamura H, Ueno H,Yamashita K, et al. Enhanced production and activation of progelatinase A mediated by membrane-type 1matrix metalloproteinase in human papillary thyroid carcinomas.Cancer Res 1999;59:467-73.
  • 10[8]Kang T, Yi J, Yang WR, et al. Functional characterization of MT3-MMP in transfected MDCK cells: progelatinase A activation and tubulogenesis in 3-D collagen lattice. FASEB J 2000;14:2559-68.

共引文献23

同被引文献32

  • 1Clark IM, Swingler TE, Sampieri CL, et al. The regulation of matrix metalloproteinases and their inhibitors[J]. Int J Biochem Cell Biol, 2008, 40(6-7): 1362-1378.
  • 2SulkaIa M, Larmas M. The IocaIization of matrix metalloproteinases -20(MMP-20,enamelysin)in mature human teeth[J]. J Dent Res, 2002, 81: 603-607.
  • 3Turk BE, Lee DH, Yamakoshi Y, et al. MMP-20 is predominately a tooth-specific enzyme with a deep catalytic pocket that hydrolyzes type V collagen[J]. Biochemistry, 2006, 45(12): 3863-3874.
  • 4Simmer JP, Hu JC. Expression, structure, and function of enamel proteinases[J]. Connect Tissue Res, 2002, 43(2-3): 441-449.
  • 5Iwata T, Yamakoshi Y, Hu JC, et al. Processing of ameloblastin by MMP-20[J]. J Dent Res, 2007,86(2): 153-157.
  • 6Park JC, Park JT, Son HH, et al. The amyloid protein APin is highly expressed during enamel mineralization and maturation in rat incisors[J]. Eur J Oral Sei, 2007,15(2): 153-160.
  • 7Bourd- Boittin K, Septier D, Hal LR, et al. Immunolocalizatian of enamelysin (matrix metalloproteinase-20) in the forming rat incisor[J]. J Histochem Cytochem, 2004, 52(4): 437- 445.
  • 8Vaananen A, Srinivas R, Parikka M, et al.Expression andregulation of MMP-20 in human tongue carcinoma cells[J]. J Dent Res, 2001, 80: 1884-1889.
  • 9Rush J, Lesot H, Begue - kirn C. Odontoblast differentiation[J]. Int J Dev Bio1,1995, 39(1): 51-68.
  • 10Smith A, Cassidy N, Perry H, et al. Reactionary dentinogenesis[J]. Int J Dev Biol, 1995, 39(1): 273-280.

引证文献2

二级引证文献4

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