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An inhibitor of urokinase and tissue plasminogen activators in Dunning R3327H prostate tumors of rats treated with D-Trp6-LH-RH.

作者信息

Hierowski M T, Schally A V

出版信息

Horm Res. 1985;21(2):124-35. doi: 10.1159/000180036.

DOI:10.1159/000180036
PMID:3156799
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.

摘要

相似文献

1
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Horm Res. 1985;21(2):124-35. doi: 10.1159/000180036.
2
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引用本文的文献

1
The primary plasminogen-activator inhibitors in endothelial cells, platelets, serum, and plasma are immunologically related.内皮细胞、血小板、血清和血浆中的主要纤溶酶原激活物抑制剂在免疫学上相关。
Proc Natl Acad Sci U S A. 1985 Dec;82(24):8710-4. doi: 10.1073/pnas.82.24.8710.