Expression of 92-kDa type IV collagenase correlates with angiogenic markers and poor survival in head and neck squamous cell carcinoma

被引:52
作者
Riedel, F [1 ]
Götte, K [1 ]
Schwalb, J [1 ]
Bergler, W [1 ]
Hörmann, K [1 ]
机构
[1] Univ Hosp Mannheim, HNO Klin, Dept Otolaryngol Head & Neck Surg, D-68135 Mannheim, Germany
关键词
matrix metalloproteinases; tumor angiogenesis; bFGF; VEGF; head and neck squamous cell carcinoma;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MMP-9, which degrades extracellular matrix, is believed to play a crucial role in tumor invasion and metastasis. Angiogenesis is also perceived as an important step in tumor growth and metastasis. The aim of this study was to investigate the expression of MMP-9 in tumor samples of HNSCC patients and to study a possible correlation to angiogenic markers. Cryostat sections of 52 HNSCC tumors were immunostained for MMP-9, bFGF and VEGF using a standard streptavidin-biotin complex procedure for light microscopic investigation. Microvessel density (MVD) was determined by staining of endothelial cells immunohistochemically using anti-vWF; monoclonal antibody. MMP-9 positive staining was detected in 27/52 (52%) of the tumors. MMP-9 immunoreactivity did not con elate with the main clinicopathological characteristics of the patients (localisation, T-stage, N-stage, histological grading), but correlated with worse survival of the patients. MMP-9 negative tumors showed a significant lower mean MVD pet microscopic field than MMP-9 positive tumors (p<0.001). There was a significant association of MMP-9 and VEGF; expression (p<0.05). The presence of MMP-9 in HNSCC cancer and the positive correlation with MVD and VEGF; expression supports the theory that MMP-9 functions as a regulator of tumor angiogenesis supporting endothelial cell invasion. MMP-9 and VEGF might act co-operatively in the process of neovascularization in human head and neck cancer.
引用
收藏
页码:1099 / 1105
页数:7
相关论文
共 40 条
[1]  
BREIER G, 1992, DEVELOPMENT, V114, P521
[2]   Localization of matrix metalloproteinase MMP-2 to the surface of invasive cells by interaction with integrin alpha v beta 3 [J].
Brooks, PC ;
Stromblad, S ;
Sanders, LC ;
vonSchalscha, TL ;
Aimes, RT ;
StetlerStevenson, WG ;
Quigley, JP ;
Cheresh, DA .
CELL, 1996, 85 (05) :683-693
[3]  
Burian M, 1999, ACTA OTO-LARYNGOL, V119, P289
[4]   Changing views of the role of matrix metalloproteinases in metastasis [J].
Chambers, AF ;
Matrisian, LM .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1997, 89 (17) :1260-1270
[5]   Expression of matrix metalloproteinases and tissue inhibitor of metalloproteinases in head and neck squamous cell carcinoma [J].
Charous, SJ ;
Stricklin, GP ;
Nanney, LB ;
Netterville, JL ;
Burkey, BB .
ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY, 1997, 106 (04) :271-278
[6]  
DRAY TG, 1996, ANN OTO RHINOL LARYN, P724
[7]  
Endo K, 1997, ANTICANCER RES, V17, P2253
[8]   INTERSTITIAL COLLAGENASE IS REQUIRED FOR ANGIOGENESIS IN-VITRO [J].
FISHER, C ;
GILBERTSONBEADLING, S ;
POWERS, EA ;
PETZOLD, G ;
POORMAN, R ;
MITCHELL, MA .
DEVELOPMENTAL BIOLOGY, 1994, 162 (02) :499-510
[9]   ANGIOGENESIS IN CANCER, VASCULAR, RHEUMATOID AND OTHER DISEASE [J].
FOLKMAN, J .
NATURE MEDICINE, 1995, 1 (01) :27-31
[10]   TUMOR ANGIOGENESIS [J].
FOLKMAN, J .
ADVANCES IN CANCER RESEARCH, 1985, 43 :175-203