期刊文献+

TFPI-2和MMP-9在非小细胞肺癌中的表达及临床意义 被引量:3

Expression and clinical significance of TFPI-2 and MMP-9 in non-small cell lung cancer
下载PDF
导出
摘要 目的:研究组织因子途径抑制物-2(tissue factor pathway inhibitor-2,TFPI-2)、基质金属蛋白酶-9(matrix metalloproteinase-9,MMP-9)在非小细胞肺癌(non-small cell lung cancer,NSCLC)中的表达及之间的相关性。方法:采用免疫组化法检测60例NSCLC组织TFPI-2和MMP-9的表达,并分析TFPI-2和MMP-9的表达水平与性别、年龄、组织类型、分化程度、肿瘤直径、TNM分期及淋巴结转移的关系。结果:NSCLC中临床分期为Ⅰ、Ⅱ、Ⅲ期的患者中TFPI-2表达阳性率分别为75.8%、25.0%和40.0%(P<0.01),无淋巴结转移和有淋巴结转移的患者中TFPI-2表达阳性率分别为66.7%、38.1%(P<0.01),肿瘤直径>5cm和≤5cm的患者TFPI-2表达阳性率分别为15.0%、77.5%(P<0.01)。临床分期为Ⅰ、Ⅱ、Ⅲ期的患者中MMP-9表达阳性率分别为48.5%、83.3%和93.3%(P<0.01),无淋巴结转移和有淋巴结转移的患者中MMP-9表达阳性率分别为56.4%、85.7%(P<0.01),肿瘤直径>5cm和≤5cm的患者MMP-9表达阳性率分别为95.0%、52.5%(P<0.01)。NSCLC组织中TFPI-2的低表达与MMP-9的高表达呈负相关(r=-0.476,P=0.001)。结论:TFPI-2的低表达和MMP-9的高表达与NSCLC临床分期、肿瘤大小及淋巴结转移密切相关。TFPI-2可能通过抑制MMP-9的表达,从而抑制NSCLC的生长、浸润和转移。 Objective:To investgate the relationship between the expression and correlation of TFPI-2 and MMP -9 in NSCLC.Methods:The expression of TFPI-2,MMP-9 was detected by immunohistochemistry in 60 patients with NSCLC.Results:In patients with NSCLC of clinical stage Ⅰ,Ⅱ,Ⅲ TFPI-2 expression positive rates were 75.8%,25.0% and 40.0% respectively(P < 0.01).TFPI-2 expression positive rates without lymph node metastasis and lymph node metastasis in patients were 66.7% and 38.1% (P<0.01).In tumor diameter > 5 cm and ≤ 5cm patients TFPI-2 expression positive rates were 15.0%,77.5% (P < 0.01).In clinical stage Ⅰ,Ⅱ,Ⅲ patients MMP-9 expression positive rates were 48.5%,83.3%,93.3% (P < 0.01) respectively.In patients without lymph node metastasis and lymph node metastasis MMP-9 expression positive rates were 56.4%,85.7% (P < 0.01).Tumor diameter > 5 cm and ≤ 5 cm patients MMP-9 expression positive rates were 95.0%,52.5% (P < 0.01).The expression of TFPI-2 and MMP-9 in NSCLC were negatively correlated (r =-0.476,P =0.001).Conclusion:The low expression of TFPI-2 and high expression of MMP-9 are closely related with NSCLC clinical stage,tumor size and lymph node metastasis.TFPI-2 could inhibit the expression of MMP-9 to prevent tumor growth,invasion and metastasis.
出处 《现代肿瘤医学》 CAS 2013年第11期2458-2460,共3页 Journal of Modern Oncology
基金 武汉市青年科技晨光计划项目(编号:201050231090)
关键词 组织因子途径抑制物-2 基质金属蛋白酶-9 非小细胞肺癌 免疫组化 tissue factor way inhibitor-2 matrix metalloproteinase-9 non-small cell lung cancer immunohistochemistry
  • 相关文献

参考文献12

二级参考文献46

  • 1李中信,贾漪涛,马顺茂,杜芸,王永军,于跃明.结直肠癌组织NF-κB和MMP-9表达与腹腔微转移关系的初步探讨[J].中华肿瘤防治杂志,2008,15(13):1014-1017. 被引量:12
  • 2牟晓燕,李怀臣,韩俊庆,黄琛,张维东.MMP_2和MMP_9在非小细胞肺癌组织中的表达[J].山东医药,2004,44(25):7-8. 被引量:8
  • 3徐飚,王建明.胃癌流行病学研究[J].中华肿瘤防治杂志,2006,13(1). 被引量:159
  • 4Littlepage LE, Sternlicht MD, Rougier N, et al. Matrix metalloproteinases contribute distinct roles in neuroendocrine prostate carcinogenesis, metastasis, and angiogenesis progression [ J]. Cancer Res, 2010,70 (06) :2224 - 2234.
  • 5Woo M, Park K, Nam J, et al. Clinical implications of matrix met- alloproteinase - 1, - 3, - 7, - 9, - 12, and plasminogen activator inhibitor - 1 gene polymorphisms in colorectal cancer[ J]. J Gastro- enterol Hepato1,2007,22 (7) : 1064 - 1070.
  • 6Mori M, Barnard GF, Mimori K, et al. Overexpression of matrix metalloproteinase -7 mRNA in human colon carcinomas [ J ]. Cancer, 1995,75(6) :1516 - 1519.
  • 7Ra H J, Parks WC. Control of matrix metaUoproteinase catalytic activity [ J ]. Matrix Biol,2007,26 (8) :587 - 596.
  • 8Gershtein ES, Korotkova EA, Shcherbakov AM, et al. Matrix metalloproteinases 7 and 9 and their types 1 and 4 tissue inhibitors in tumors and plasma of patients with colorectal cancer[ J ]. Bull Exp Biol Med, 2007,143(4) :459 -462.
  • 9Tsunezumi J, Higashi S, Miyazaki K J, et al. Matrilysin ( MMP - 7 ) cleaves C -type lectin domain family 3 member A (CLEC3A) on tumor cell surface and modulates its cell adhesion activity[ J]. Cell Biochem, 2009,106 (4) : 693 - 702.
  • 10Styhanou S, Clarke RB, Brennan K. Abenant activation of notch signaling in hanoi breast cancer. Cancer Res, 2006, 66 : 1517-1525.

共引文献22

同被引文献27

引证文献3

二级引证文献6

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