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The secretion of urokinase‐like plasminogen activator is inhibited by microtubule‐interacting drugs
Author(s) -
Santibañez Juan F.,
Maccioni Ricardo B.,
Martínez Jorge
Publication year - 1995
Publication title -
cell biochemistry and function
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.933
H-Index - 61
eISSN - 1099-0844
pISSN - 0263-6484
DOI - 10.1002/cbf.290130313
Subject(s) - microtubule , secretion , plasminogen activator , gelatinase , cytoskeleton , tubulin , microbiology and biotechnology , urokinase , extracellular , chemistry , matrix metalloproteinase , biology , biochemistry , cell , endocrinology , genetics
The secretion of proteinases into the extracellular matrix is one of the main features of tumour cells, as related to their invasive behaviour. Considering the role of the microtubule cytoskeleton, and particularly the action of microtubule‐associated protein (MAPs) in mediating protein secretion, the effects of the anti‐microtubule drugs estramustine and taxol, on the secretion of urokinase‐type plasminogen activator (u‐PA) and the 72 kDa gelatinase were investigated. Treatment of 5637 bladder carcinoma cells with estramustine and taxol inhibited u‐PA secretion into the conditioned medium in a drug concentration‐dependent fashion. This inhibition was confirmed by determinations of u‐PA enzymatic activities and by measurements of the levels of immunoreactive activator. Studies using gelatin zymograms also showed an inhibition of another tumoural proteinase namely the 72 kDa gelatinase. Time‐course uptake experiments showed that estramustine was incorporated into the cells, a process which depended on temperature. On the other hand, immunofluorescence studies indicated that the microtubule network was affected by taxol with the formation of bundles of microtubules at different cell domains. Minor effects were visualized after treatment of the cells with estramustine‐phosphate, a drug that blocks primarily the action of microtubule‐associated proteins. The studies provide a way to analyse the relationships between u‐PA secretion and the integrity of the cytoskeletal network.