Expression of matrix metalloproteinases 7 and 9 in non-small cell lung cancer -: Relation to clinicopathological factors, β-catenin and prognosis

被引:64
作者
Leinonen, T
Pirinen, R
Böhm, J
Johansson, R
Ropponen, K
Kosma, VM
机构
[1] Univ Kuopio, Dept Pathol & Forens Med, FIN-70211 Kuopio, Finland
[2] Kuopio Univ Hosp, FIN-70211 Kuopio, Finland
[3] Univ Kuopio, Dept Oncol, FIN-70211 Kuopio, Finland
关键词
MMP-7; MMP-9; lung cancer; beta-catenin; prognosis;
D O I
10.1016/j.lungcan.2005.11.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Matrix metalloproteinases (MMPs) have been shown to have a significant rote in determining cancer cell behaviour. The present study was undertaken to analyze the expression and prognostic value of MMP-7 and MMP-9 in non-small cell lung cancer (NSCLC). The relationship of MMP-7 with P-catenin was also evaluated. The study consists of 212 patients with resected NSCLC. Tumour samples were stained immunohistochemicalty, and the expression of MMP-7 and MMP-9 was evaluated in both tumour cells and peritumoural stromal tissue. The results were compared to clinicopathological, factors of the patients. A high staining of MMP-7 and MMP-9 in tumour cells was noted in 62 (30%) and 113 (57%) cases, respectively. Expression of MMP-7 was noted more often in adenocarcinomas than in other histological types (p = 0.022). High cancer cell associated MMP-7 was related to Lower T-factor (p = 0.037), better tumour differentiation (p = 0.005) and normal beta-catenin expression in tumour cells (p = 0.001). A high MMP-9 expression in tumour cells was related to poor tumour differentiation (p = 0.016). The stromal signal for MMP-9 was observed in 58 (32%) cases and was linked with higher tumour grade (p = 0.031). In survival analyses the significant predictors of survival were histological type of tumour and tumour stage (p = 0.0009 and 0.0012, respectively). MMP-7 or MMP-9 signals were not related to patient's outcome. The results show that high MMP-9 expression indicates aggressive, and high MMP-7 Less aggressive tumour behaviour in NSCLC. However, MMP-7 and MMP-9 expressions had no prognostic value in NSCLC. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:313 / 321
页数:9
相关论文
共 47 条
[21]   Matrilysin (MMP-7) as a significant determinant of malignant potential of early invasive colorectal carcinomas [J].
Masaki, T ;
Matsuoka, H ;
Sugiyama, M ;
Abe, N ;
Goto, A ;
Sakamoto, A ;
Atomi, Y .
BRITISH JOURNAL OF CANCER, 2001, 84 (10) :1317-1321
[22]   Tumour cell and stromal features in metastatic and non-metastatic non-small cell lung carcinomas [J].
Minamoto, H ;
Antonângelo, L ;
da Silva, AGP ;
Gallo, CP ;
Silva, FBDE ;
Fenezelian, S ;
Rodrigues, OR ;
Jatene, F ;
Saldiva, P ;
Capelozzi, VL .
HISTOPATHOLOGY, 2003, 43 (05) :427-443
[23]   Secreted MMP9 promotes angiogenesis more efficiently than constitutive active MMP9 bound to the tumor cell surface [J].
Mira, E ;
Lacalle, RA ;
Buesa, JM ;
de Buitrago, GG ;
Jiménez-Baranda, S ;
Gómez-Moutón, C ;
Martínez, C ;
Mañes, S .
JOURNAL OF CELL SCIENCE, 2004, 117 (09) :1847-1856
[24]   Regulation of matrix biology by matrix metalloproteinases [J].
Mott, JD ;
Werb, Z .
CURRENT OPINION IN CELL BIOLOGY, 2004, 16 (05) :558-564
[25]  
Nawrocki B, 1997, INT J CANCER, V72, P556, DOI 10.1002/(SICI)1097-0215(19970807)72:4<556::AID-IJC2>3.0.CO
[26]  
2-P
[27]   Oncogenic β-catenin and MMP-7 (matrilysin) cosegregate in late-stage clinical colon cancer [J].
Ougolkov, AV ;
Yamashita, K ;
Mai, M ;
Minamoto, T .
GASTROENTEROLOGY, 2002, 122 (01) :60-71
[28]   Expression of matrix metalloproteinase (MMP)-2 and MMP-9 in breast cancer with special reference to activator protein-2, HER2, and prognosis [J].
Pellikainen, JM ;
Ropponen, KM ;
Kataja, VV ;
Kellokoski, JK ;
Eskelinen, MJ ;
Kosma, VM .
CLINICAL CANCER RESEARCH, 2004, 10 (22) :7621-7628
[29]  
Pinto CA, 2003, CLIN CANCER RES, V9, P3098
[30]   Reduced expression of CD44v3 variant isoform is associated with unfavorable outcome in non-small cell lung carcinoma [J].
Pirinen, R ;
Hirvikoski, P ;
Böhm, J ;
Kellokoski, J ;
Moisio, K ;
Virén, M ;
Johansson, R ;
Hollmén, S ;
Kosma, VM .
HUMAN PATHOLOGY, 2000, 31 (09) :1088-1095