An Inhibitor of Urokinase and Tissue Plasminogen Activators in Dunning R3327H Prostate Tumors of Rats Treated with D-Trp6-LH-RH
- 1 January 1985
- journal article
- research article
- Published by S. Karger AG in Hormone Research
- Vol. 21 (2) , 124-135
- https://doi.org/10.1159/000180036
Abstract
The antifibrinolytic activity of cytosol from Dunning R3327H rat prostate tumors was studied. The prostate tumors from rats treated with D-Trp6-LH-RH had 2.5 times lower plasminogen activator activity than tumors from untreated rats. This was due to the presence of an inhibitor of plasminogen activator as well as a reduction in residual activity of plasminogen activator(s). Only the cytosolic extracts from prostate tumors of rats treated with D-Trp6-LH-RH contained this inhibitor. The purified inhibitor (m.w. 21,000), formed a complex with urokinase and partially purified plasminogen activator(s) from prostate tumors of untreated as well as D-Trp6-LH-RH treated rats. The increase in antifibrinolytic activity after treatment with LH-RH analogs may be an important factor in reducing the invasiveness of the prostate tumor.Keywords
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