Literature DB >> 2467971

Inhibition of guanidinobenzoatase by a substrate for trypsin-like enzymes.

F S Steven1, M M Griffin, W F Mangel, H Maier, M Altmannsberger.   

Abstract

Guanidinobenzoatase is a proteolytic enzyme capable of degrading fibronectin and is a tumour associated enzyme. Guanidinobenzoatase has been shown to be an arginine selective protease and is distinct from trypsin, plasmin and thrombin, the latter enzymes can be assayed with bis(carbobenzyloxycarbonyl-L-argininamido)-Rhodamine or BZAR. Guanidinobenzoatase is inhibited by BZAR when the enzyme is assayed in free solution and when the enzyme is cell-bound in frozen sections of tumour containing tissues. It is proposed that BZAR and its analogues may be of value in inhibiting tumour cell invasion in vivo and also that the selectivity of BZAR may be used to direct cytotoxic drugs to tumour cells possessing active guanidinobenzoatase.

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Year:  1988        PMID: 2467971     DOI: 10.3109/14756368809040727

Source DB:  PubMed          Journal:  J Enzyme Inhib        ISSN: 1026-5457


  2 in total

1.  The status of trypsin-like enzymes in squamous-cell carcinoma of the head and neck region.

Authors:  F S Steven; L A Williams; H Maier; J Arndt; H Weidauer; A Born
Journal:  J Cancer Res Clin Oncol       Date:  1990       Impact factor: 4.553

2.  A study of guanidinobenzoatase during development of mesothelioma induced in the rat by fibrous erionite.

Authors:  F S Steven; R J Hill
Journal:  Br J Cancer       Date:  1988-11       Impact factor: 7.640

  2 in total

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