The plasminogen-plasminogen activator (PA) system in neuroblastoma : Role of PA inhibitor-1 in metastasis

• Published in: Cancer research (Chicago, Ill.) Ill.), 1999-03, Vol.59 (6), p.1327-1336
• Main Authors: SUGIURA, Y, LIQUN MA, BO SUN, SHIMADA, H, LAUG, W. E, SEEGER, R. C, DECLERCK, Y. A
• Format: Article
• Language: English
• Subjects: Biological and medical sciences; Cell Adhesion - drug effects; Cell Movement - drug effects; Endothelium - metabolism; Fibronectins - physiology; Humans; Medical sciences; Neoplasm Metastasis; Neoplasm Recurrence, Local; Neuroblastoma - metabolism; Neuroblastoma - pathology; Neuroblastoma - secondary; Neurology; Plasminogen - biosynthesis; Plasminogen - physiology; Plasminogen Activator Inhibitor 1 - biosynthesis; Plasminogen Activator Inhibitor 1 - physiology; Plasminogen Activators - biosynthesis; Plasminogen Activators - physiology; RNA, Messenger - biosynthesis; Stromal Cells - metabolism; Tumor Cells, Cultured; Tumors of the nervous system. Phacomatoses; Vitronectin - physiology
• ISSN: 0008-5472; 1538-7445

Proteases of the plasminogen-plasminogen activator (PA) system play an important role in cancer metastasis. We have examined the expression of these proteases and their cell surface receptors and inhibitors in neuroblastoma, a tumor that originates in cells of the neural crest and is the second most common solid tumor in children. This analysis was performed in seven established human cell lines and 20 primary tumor specimens. Urokinase PA and, in particular, tissue-type PA were expressed in cell lines and in tumor tissues; however, their levels of expression did not correlate with clinical stage. There was little evidence suggesting that neuroblastoma cells concentrate PA activity at their cell surface because urokinase-type PA receptor mRNA was detected in two cell lines and in 5 of 20 tumor samples by reverse transcription-PCR only. PA inhibitor (PAI)-2 was absent in all cell lines and tumor tissue samples examined. However, PAI-1, which was not expressed by the cell lines, was expressed by stromal cells and, specifically, endothelial cells in tumor tissue. By extending the analysis of PAI-1 expression in 64 primary tumor specimens, we found that high PAI-1 expression paradoxically correlated with metastatic stage and tumor recurrence. In vitro experiments indicated that the expression of PAI-1 by human microvascular endothelial cells was stimulated in the presence of SK-N-BE(2) human neuroblastoma cells and neuroblastoma culture medium. Recombinant PAI-1 also promoted SK-N-BE(2) cell detachment from vitronectin and migration from vitronectin toward fibronectin. From these data, we conclude that the up-regulation of PAI-1 expression in endothelial cells may promote rather than inhibit metastasis in neuroblastoma.