Expression of inducible nitric oxide synthase in bone metastases

被引:9
作者
Brennan, RA
Sharma, S
Bowden, JR
Umar, T
机构
[1] Queen Alexandra Hosp, Maxillofacial Unit, Portsmouth PO6 3LY, Hants, England
[2] Queen Alexandra Hosp, Translat Oncol Res Lab, Portsmouth PO6 3LY, Hants, England
[3] St Richards Hosp, Dept Oral & Maxillofacial Surg, Chichester PO19 4SE, W Sussex, England
来源
EUROPEAN JOURNAL OF SURGICAL ONCOLOGY | 2003年 / 29卷 / 07期
关键词
nitric oxide; bone; metastasis;
D O I
10.1016/S0748-7983(03)00105-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aims: The signalling molecule nitric oxide (NO), produced predominantly in cancer by the enzyme inducible NO synthase (iNOS), has been implicated in the pathophysiology of many human tumours. The increased NO concentrations found in many human cancers may facilitate both angiogenesis and tumour dissemination. NO also plays a concentration-dependent role in bone re-modelling by acting on osteoclasts. Although iNOS has been studied extensively in most primary tumours, there are no reports that have investigated its expression in metastatic bone disease. Methods: An immunohistochemical study was performed using a monoclonal antibody to iNOS in 27 cases of breast, renal and lung bone metastases, biopsied at the time of treatment for pathological fracture. Results: iNOS expression was found in 14 cases and was predominantly localised to tumour cells in the metastatic deposits. A significant difference was found between iNOS expression in metastases and adjacent bone (p < 0.001), where immunostaining was rarely seen and confined to immune cells. No microscopic differences in bone architecture could be seen between iNOS positive and negative metastases, and no correlations were found between iNOS expression and clinico-pathological variables. Conclusions: iNOS expression is not a pathognomonic finding in bone metastasis. Its role in the behaviour of bone metastases requires further investigation. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:619 / 623
页数:5
相关论文
共 25 条
[1]   P53 and vascular endothelial growth factor regulate tumor growth of NOS2-expressing human carcinoma cells [J].
Ambs, S ;
Merriam, WG ;
Ogunfusika, MO ;
Bennett, WP ;
Ishibe, N ;
Hussain, SP ;
Tzeng, EE ;
Geller, DA ;
Billiar, TR ;
Harris, CC .
NATURE MEDICINE, 1998, 4 (12) :1371-1376
[2]  
Brennan PA, 2001, HEAD NECK-J SCI SPEC, V23, P217, DOI 10.1002/1097-0347(200103)23:3<217::AID-HED1021>3.0.CO
[3]  
2-#
[4]   Nitric oxide is a regulator of bone remodelling [J].
Chae, HJ ;
Park, RK ;
Chung, HT ;
Kang, JS ;
Kim, MS ;
Choi, DY ;
Bang, BG ;
Kim, HR .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1997, 49 (09) :897-902
[5]   Nitric oxide acts in conjunction with proinflammatory cytokines to promote cell death in osteoblasts [J].
Damoulis, PD ;
Hauschka, PV .
JOURNAL OF BONE AND MINERAL RESEARCH, 1997, 12 (03) :412-422
[6]   CYTOKINES INDUCE NITRIC-OXIDE PRODUCTION IN MOUSE OSTEOBLASTS [J].
DAMOULIS, PD ;
HAUSCHKA, PV .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 201 (02) :924-931
[7]  
DONG ZY, 1994, CANCER RES, V54, P789
[8]  
DuenasGonzalez A, 1997, MODERN PATHOL, V10, P645
[9]   Tumor cell nitric oxide inhibits cell growth in vitro, but stimulates tumorigenesis and experimental lung metastasis in vivo [J].
Edwards, P ;
Cendan, JC ;
Topping, DB ;
Moldawer, LL ;
MacKay, S ;
Copeland, EM ;
Lind, DS .
JOURNAL OF SURGICAL RESEARCH, 1996, 63 (01) :49-52
[10]   WHAT IS THE EVIDENCE THAT TUMORS ARE ANGIOGENESIS DEPENDENT [J].
FOLKMAN, J .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1990, 82 (01) :4-6