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Expression of plasminogen activators and plasminogen activator inhibitor 1 in dedifferentiated chondrosarcoma

✍ Scribed by Carsten Häckel; Bogdan Czerniak; Alberto G. Ayala; Kathrin Radig; Albert Roessner


Publisher
John Wiley and Sons
Year
1997
Tongue
English
Weight
474 KB
Volume
79
Category
Article
ISSN
0008-543X

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✦ Synopsis


Background:

The plasminogen activator system plays an important role in different malignant tumors. these enzymes participate in the destruction of intercellular matrices and basement membranes and/or can modulate the growth potency of tumor cells and may even promote metastases. in this study, the expression of three glycoproteins that play a role in the plasminogen activator system as activators of proteolysis-urokinase type plasminogen activator (u-pa), tissue type plasminogen activator (t-pa), and plasminogen activator inhibitor type 1 (pai-1) were studied in various components of dedifferentiated chondrosarcomas of bone.

Methods:

The expression of u-pa, t-pa, and pai-1 was investigated in 10 dedifferentiated chondrosarcomas and 14 conventional chondrosarcomas. the plasminogen activator/inhibitor glycoproteins were visualized immunohistochemically on paraffin sections and the levels of expression were assessed semiquantitatively.

Results:

In dedifferentiated chondrosarcoma, high grade dedifferentiated components displayed strong, diffuse coexpression of u-pa, t-pa, and pai-1. for all glycoproteins studied, the immunoreactivity was significantly increased compared with the reactions in the low grade cartilaginous component of the same tumor and conventional chondrosarcoma. in the latter, u-pa, t-pa, and pai-1 expression was found to be enhanced at invasive foci and in regions of endochondral ossification.

Conclusions:

The current study documents the overexpression of u-pa, t-pa, and pai-1 in dedifferentiated chondrosarcoma and suggests involvement of the plasminogen activator system in the biology of these tumors.


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Plasminogen activator (PA) and PA inhibitor (PAI) were measured in homogenates of leukemia cells. Both PA and PA1 levels were higher in non-lymphobiastic leukemia than in lymphobiastic leukemia. The levels were below the sensitivity of determination in chronic myeiocytic leukemia (CML) but showed si