Urokinase (Abbokinase), also called urokinase-type Plasminogen Activator (uPA), is a
serine protease (). Urokinase was originally isolated from human
urine, but is present in several physiological locations, such as blood stream and the
extracellular matrix. The primary physiological substrate is
plasminogen, which is an inactive
zymogen form of the serine protease
plasmin. Activation of plasmin triggers a proteolysis cascade which, depending on the physiological environment participate in
thrombolysis or
extracellular matrix degradation. This links urokinase to vascular diseases and cancer.
Molecular characteristics
Urokinase is a 411
residue protein, consisting of three
domains: the serine protease domain, the
kringle domain and the
growth factor domain. Urokinase is synthesized as a zymogen form (prourokinase or single chain urokinase), and is activated by proteolytic cleavage between L158 and I159. The two resulting chains are kept together by a
disulfide bond.
Interaction partners
The most important inhibitors of urokinase are the
serpins plasminogen activator inhibitor-1 (PAI-1) and
plasminogen activator inhibitor-2 (PAI-2), which inhibits the protease activity irreversibly. In the extracellular matrix urokinase is tethered to the
cell membrane by its interaction to the
urokinase receptor.
Urokinase and cancer
Elevated
expression levels of urokinase and several other components of the
plasminogen activation system are found to be correlated with
tumor malignancy. It is believed that the tissue degradation following plasminogen activation, facilitates tissue invasion and thus contributes to
metastasis. This makes urokinase an attractive
drug target and
inhibitors have been sought to be used as anticancer agents. However incompatibilities between the human and
murine system hampers clinical evaluation of these agents. Through its interaction with the
urokinase receptor, urokinase affects several other aspects of cancer biology such as cells adhesion, migration and cellular
mitotic pathways.
Clinical applications
Urokinase is used clinically as a
thrombolytic agent in the treatment of severe or massive
deep venous thrombosis,
pulmonary embolism,
myocardial infarction, and occluded
intravenous or
dialysis cannulas. It is also administered intrapleurally to improve the drainage of complicated pleural effusions and empyemas. Recently,
Alteplase has replaced urokinase as a thrombolytic drug in infarctation.