期刊文献+

基质金属蛋白酶在早期肺癌中的表达 被引量:10

The expression of matrix metalloproteinases in early stage no-small-cell lung cancer
原文传递
导出
摘要 目的探讨早期肺癌中的基质金属蛋白酶(MMP)-9、MMP-2、MMP-7活性及与MMP抑制剂开发的关系。方法采用明胶酶谱及酪素酶谱法测定60例Ⅰ期非小细胞肺癌(NSCLC)患者的肺肿瘤及对应正常肺组织中MMP-9、MMP-2、MMP-7的活性。结果MMP-9活性均见于正常及癌组织中,但早期肺癌组织中的MMP-9的活性为(1189.3±537.0)灰度值,低于正常对照肺组织中(1557.7±422.5)灰度值(P〈0.05)。肿瘤的MMP-2的活性率(62kDa/62kDa+66kDa)(45.5±8.4)%明显高丁相对应的正常组织中的(25.9±10.5)%(P〈0.01)。阳性对照的人羊水标本在酪素酶谱凝胶上显示MMP-7约20kI)a的透明活性带,但同时肺癌及正常肺组织标本未显示出MMP-7的可检测的活性。结论早期肺癌组织中MMP-9活性低及无明显MMP-7活性,MMP-2活性显著增高。 Objective To investigate the activity of matrix metalloproteinases (MMP)-9, -2, -7 in non-small cell lung cancer (NSCLC) and the interrelationship between the expression of MMP and MMP inhibitor (MMPI) development. Methods The activity of MMP-2, MMP-9 and MMP-7 in 60 cases of stage Ⅰ NSCLC (36 cases of stage Ia, 24 cases of Ib 24 ; 25 cases of squamous carcinoma, 35 cases of adenocarcinoma) was measured by using gelatin zymography or casein zymography. Results The MMP-9 activity could be checked in hmg cancer tissue and normal tissue. However, in early stage NSCLC the average activity of MMP-9 ( 1189.3 ±537.0 pixel) was lower than in control normal lung tissue ( 1557.7 ±422. 5 pixel), P 〈 0. 05. The MMP-2 activity rate in tumor (62 kDa/62 kDa + 66 kDa) (45.5 ±8.4 )% was significantly higher than that in normal lung cancer tissue (25.9 ± 10. 5)% (P 〈0. 01 ). On casein zymography gel, the active MMP-7 in amniotic fluid showed a lucid band as 20 kDa, but no any detectable MMP-7 activity was found in lung cancer tissue and normal tissue. Conclusion In early stage of NSCLC, MMP-9 activity was low, there was no obvious MMP-7 activity, and the MMP-2 activity was significantly increased.
出处 《中华实验外科杂志》 CAS CSCD 北大核心 2010年第5期612-613,共2页 Chinese Journal of Experimental Surgery
关键词 基质金属蛋白酶抑制剂 肺癌 MMP inhibitor Lung carcinoma
  • 相关文献

参考文献7

二级参考文献48

  • 1Fang J, Shing Y, yan L, et al. Matrix metalloproteinase-2 is required for switch to the angiogenic phentype in a tumor model[J].Proc Natl Acad Sci USA,2000,97(8) :3884-3889. 被引量:1
  • 2Kajita M, hoh Y,Chibab T, et al. Membrance-type 1 matrix metalloproteinase cleaves CIM4 and promotes cell migration[ J ]. J Cell Biol, 2001,153 (5) : 893-940. 被引量:1
  • 3Kriiger A, Fata JE, Khokha R. Altered tumor growth and metastasis of a T-cell lymphoma in Timp-1 transgenic mice[J]. Blood, 1997,90(5) : 1993-2000. 被引量:1
  • 4Kruger A, Martin DC, Fata JE, et al. Host TIMP-1 overexpression confers resistance to experimental brain metastasis of a bibrosarcomacell line[J]. Oncogene, 1998,16(18) :2419-2423. 被引量:1
  • 5Soloway PD, Alexander C, Werb Z, et al. Targeted mutagenesis of TIMP-1 reveals that hmg tumor invasion is influence by Timp-1 genetype of the tumor but not by that of the host[J]. Oncogene,1996,13(11) ; 2307-2314. 被引量:1
  • 6Sheu BC, Hsu SM, Ho HM, et al. A novel role of meyralloproteinase in cancer-mediated imrnunosuppression [ J ]. Cancer Res, 2001,61 ( 1 ) : 237-242. 被引量:1
  • 7Gorelik L, Flavell RA. Immune-mediated eradication of tumors through the blockade of transforming growth factor-βsignaling in T cells[ J ]. Nature Med, 2001,7 (10) : 1118-1122. 被引量:1
  • 8Muller A, Homey B, Soto H, et al. Involvement of chemokin receptors in breast cancer metastasis [ J ]. Nature, 2001,410 ( 3 ) : 50-56. 被引量:1
  • 9Yonemura Y,Endo Y,Fujita H, et al. Inhibition of peritoneal dissemination in human gastric cancer by MMP-7-specific antisense oligonucleotide[J]. J Exp Clin Cancer Res,2001,20(2) :205-212. 被引量:1
  • 10Silletti S, Kessler T, Goldberg J, et al. Disruption of matrix metalloproteinase 2 binding to intergrin αvβ3 by an organic molecule inhibits angiogenesis and tumor growth in vivo[J]. Proc Natl Acad Sci USA,2001,98(1) : 119-124. 被引量:1

共引文献11

同被引文献82

引证文献10

二级引证文献58

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