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Factor Xa: at the crossroads between coagulation and signaling in physiology and disease
- Source :
- Trends in Molecular Medicine. 14:429-440
- Publication Year :
- 2008
- Publisher :
- Elsevier BV, 2008.
-
Abstract
- Activated factor Xa (FXa) is traditionally known as an important player in the coagulation cascade responsible for thrombin generation. Long considered a passive bystander, it is now evident that FXa exerts direct effects on a wide variety of cell types via activation of its two main receptors, protease-activated receptor-1 (PAR-1) and PAR-2. Recent findings suggest that PAR-2 plays a crucial role in fibro-proliferative diseases such as fibrosis, tissue remodeling and cancer and point towards FXa as the important mediator coordinating the interface between coagulation and disease progression. Here, we provide an overview of the FXa signaling pathways that mediate its effects in pathophysiology and explore the potential therapeutic implications of targeting FXa; in terms of arresting disease progression, the modulation of FXa activity might be more important than the modulation of FVIIa or thrombin. Non-hemostatic functions of FXa in health and disease: old thoughts and new developments
- Subjects :
- INDUCED DNA-SYNTHESIS
SMOOTH-MUSCLE-CELLS
Biology
Models, Biological
FACTOR PATHWAY INHIBITOR
Tissue factor
Mediator
Thrombin
Bystander effect
medicine
Animals
Humans
Receptor, PAR-2
Receptor, PAR-1
Receptor
Blood Coagulation
Molecular Biology
Protease-activated receptor 2
PROTEASE-ACTIVATED RECEPTOR-2
Neovascularization, Pathologic
BREAST-CANCER CELLS
MOLECULAR-WEIGHT HEPARIN
FACTOR-VIIA
TISSUE-FACTOR
FACTOR CYTOPLASMIC DOMAIN
Cell biology
Coagulation
Factor Xa
Immunology
Molecular Medicine
IDIOPATHIC PULMONARY-FIBROSIS
Signal transduction
Signal Transduction
medicine.drug
Subjects
Details
- ISSN :
- 14714914
- Volume :
- 14
- Database :
- OpenAIRE
- Journal :
- Trends in Molecular Medicine
- Accession number :
- edsair.doi.dedup.....c92b14f490b8e0a5c7b60ecb2b44d162
- Full Text :
- https://doi.org/10.1016/j.molmed.2008.08.001