Different patterns of angiogenesis in sarcomas and carcinomas

Citation
J. Tomlinson et al., Different patterns of angiogenesis in sarcomas and carcinomas, CLIN CANC R, 5(11), 1999, pp. 3516-3522
Citations number
22
Categorie Soggetti
Oncology
Journal title
CLINICAL CANCER RESEARCH
ISSN journal
10780432 → ACNP
Volume
5
Issue
11
Year of publication
1999
Pages
3516 - 3522
Database
ISI
SICI code
1078-0432(199911)5:11<3516:DPOAIS>2.0.ZU;2-H
Abstract
Solid tumors depend on angiogenesis for growth and metastasis, It has been shown that blood vessel density, as determined by counting the number of ca pillaries in clustered bursts, is a significant prognostic factor in carcin omas. It is unclear, however, whether vessel density is a prognostic factor in sarcomas, In this study, we examined angiogenesis in sarcomas of variou s grades and compared their vascular patterns to those of carcinomas. Micro vessels were identified by von Willebrand factor staining. The matrix of mu ltiple sarcoma and breast carcinoma specimens were extracted and subjected to Western analysis of various angiogenic factors and inhibitors. Metallopr oteinase inhibitor presence was also determined by in situ hybridization, I n breast carcinomas, capillaries were clustered in bursts within the stroma of the tumor, whereas the sarcoma capillaries were homogeneously distribut ed in the tumor stroma, Random blood vessel density per high power field in sarcomas did not correlate with patient prognosis. The matrix of sarcomas and carcinomas contained both angiogenic stimulators and inhibitors. Tissue inhibitor of metalloproteinase-l was found predominantly in fibroblasts an d myofibroblasts in the matrix of carcinoma specimens, The difference in th e pattern of angiogenesis in sarcomas and carcinomas may be attributable to the presence of fibroblasts and myofibroblasts in carcinomas, resulting in the compartmentalization of bursts of angiogenic factors. The homogeneous appearance of vessel density in sarcomas observed in the present study woul d be the consequence of the influence of a single compartment.