[Thrombin induced tumour growth - pharmacological control].
Hamostaseologie. 2007 May; 27(2):105-10.H

Abstract

The central enzyme of blood coagulation, the serine proteinase thrombin, is capable to modify the growth of tumour cells by interaction with protease activated receptors 1 and 4 of the tumour cells. Thrombin is permanently available in tumour micro environment; meizothrombin is generated from prothrombin at a tumour specific activation complex and can influence tumour cell growth via PAR-1 and 7-transdomain protein receptor signalling pathway, too. PEG-coupled direct thrombin inhibitors that possess special pharmacokinetic characteristics and that have been designed for long lasting efficacy in extracellular space, control serine proteinase activity in tumour micro environment and therefore they own a high potential anti-tumour efficacy. In xenographic tumour models this new substance class has shown a significant carcinostatic effect.

Authors+Show Affiliations

Nowak G
AG Pharmakologische Hämostaseologie, Medizinische Fakultät, Friedrich-Schiller-Universität Jena, Drackendorfer Str. 1, 07747 Jena.
Lopez M
No affiliation info available
Zieger M
No affiliation info available

MeSH

Amino Acid SequenceCell DivisionHirudinsHumansModels, MolecularMolecular Sequence DataNeoplasmsProtein ConformationReceptor, PAR-1Receptors, ThrombinSignal TransductionThrombin

Pub Type(s)

English Abstract
Journal Article

Language

ger

PubMed ID

17479173