Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3-4
pubmed:dateCreated
2009-1-29
pubmed:abstractText
Protease-activated receptors (PARs) are G-protein-coupled receptors (GPCRs) that are activated by a unique proteolytic mechanism. Besides the important role of blood coagulation factors in preventing bleeding after vascular injury, these serine proteinases actively engage target cells thereby fulfilling critical functions in cell biology. Cellular responses triggered by coagulation factor-induced PAR activation suggest that PARs play an important role in proliferation, survival and/or malignant transformation of tumor cells. Indeed, PAR expression correlates with cancer malignancy and clinical studies show that anticoagulant treatment is beneficial in cancer patients. In this review, we provide an overview on the PAR family, their mode of activation and mechanisms by which PAR signaling is terminated. In addition, we discuss the relationship between blood coagulation and cancer biology focusing on the potential role of PAR-induced modulation of cell survival, apoptosis and tumor growth.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
1424-8840
pubmed:author
pubmed:copyrightInfo
Copyright 2009 S. Karger AG, Basel.
pubmed:issnType
Electronic
pubmed:volume
36
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
137-47
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:19176987-Amino Acid Sequence, pubmed-meshheading:19176987-Animals, pubmed-meshheading:19176987-Apoptosis, pubmed-meshheading:19176987-Blood Coagulation Factors, pubmed-meshheading:19176987-Caspases, pubmed-meshheading:19176987-Cell Division, pubmed-meshheading:19176987-Cell Transformation, Neoplastic, pubmed-meshheading:19176987-Conserved Sequence, pubmed-meshheading:19176987-Enzyme Activation, pubmed-meshheading:19176987-Heterotrimeric GTP-Binding Proteins, pubmed-meshheading:19176987-Humans, pubmed-meshheading:19176987-Mice, pubmed-meshheading:19176987-Mice, Knockout, pubmed-meshheading:19176987-Models, Molecular, pubmed-meshheading:19176987-Molecular Sequence Data, pubmed-meshheading:19176987-Neoplasm Proteins, pubmed-meshheading:19176987-Neoplasms, pubmed-meshheading:19176987-Protein Conformation, pubmed-meshheading:19176987-Protein Structure, Tertiary, pubmed-meshheading:19176987-Receptors, Proteinase-Activated, pubmed-meshheading:19176987-Rhodopsin, pubmed-meshheading:19176987-Sequence Alignment, pubmed-meshheading:19176987-Sequence Homology, Amino Acid, pubmed-meshheading:19176987-Signal Transduction, pubmed-meshheading:19176987-Thrombophilia, pubmed-meshheading:19176987-Thromboplastin
pubmed:year
2008
pubmed:articleTitle
Protease-activated receptors, apoptosis and tumor growth.
pubmed:affiliation
Center for Experimental and Molecular Medicine, Academic Medical Center, Amsterdam, The Netherlands. K.S.Borensztajn@amc.uva.nl
pubmed:publicationType
Journal Article, Review