Cerebral Cavernous Malformation: From Mechanism to Therapy.
Circ Res
; 129(1): 195-215, 2021 06 25.
Article
em En
| MEDLINE
| ID: mdl-34166073
ABSTRACT
Cerebral cavernous malformations are acquired vascular anomalies that constitute a common cause of central nervous system hemorrhage and stroke. The past 2 decades have seen a remarkable increase in our understanding of the pathogenesis of this vascular disease. This new knowledge spans genetic causes of sporadic and familial forms of the disease, molecular signaling changes in vascular endothelial cells that underlie the disease, unexpectedly strong environmental effects on disease pathogenesis, and drivers of disease end points such as hemorrhage. These novel insights are the integrated product of human clinical studies, human genetic studies, studies in mouse and zebrafish genetic models, and basic molecular and cellular studies. This review addresses the genetic and molecular underpinnings of cerebral cavernous malformation disease, the mechanisms that lead to lesion hemorrhage, and emerging biomarkers and therapies for clinical treatment of cerebral cavernous malformation disease. It may also serve as an example for how focused basic and clinical investigation and emerging technologies can rapidly unravel a complex disease mechanism.
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Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Veias Cerebrais
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Hemangioma Cavernoso do Sistema Nervoso Central
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Mutação
Limite:
Animals
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Humans
Idioma:
En
Revista:
Circ Res
Ano de publicação:
2021
Tipo de documento:
Article