Why the study?
What is the role of thrombin in the pathophysiology and clinical course of glioblastomas?
What is the role of thrombin in the pathophysiology and clinical course of glioblastomas?
This review highlights the detrimental role of thrombin in the pathogenesis and progression of glioblastoma, suggesting it as a potential area for further research.
Thrombin's CNS roles suggest potential targets in neurodegeneration and stroke; leaves open therapeutic translation pending prospective studies.
Prothrombin and its active derivative thrombin are key members of the coagulation system. The only site of extra-hepatic thrombin expression is the central nervous system (CNS), where it is involved in brain development, protection, and regeneration. Thrombin affects various degenerative and ischemic CNS diseases like Alzheimer's, multiple sclerosis, cerebral ischemia, and hemorrhage in a dose dependent manner. Additionally, the association of thrombin with various malignancies has recently become evident. Thrombin facilitates the interaction between tumor cells with platelets, endothelial cells, and the adhesion to matrix proteins in various tumor types. Consequently, thrombin enables tumor cell seeding and metastasis, resulting in increased tumor cell growth and angiogenesis. Despite the exceptional position of thrombin in the CNS, its involvement in brain tumor course and development has so far been largely neglected. Over the last decade, several studies found a detrimental effect of thrombin in the most devastating of all primary brain tumors, glioblastomas (GBM). This review highlights the current knowledge on the involvement of thrombin in the pathophysiology and clinical course of GBMs.
No takes yet. Share an insight, caveat, or question.
Krenzlin et al. (2017) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: