Cerebral arteriovenous malformations. Part 1: cellular and molecular biology

被引:58
作者
Moftakhar, Parham [2 ]
Hauptman, Jason S. [1 ]
Malkasian, Dennis [1 ]
Martin, Neil A. [1 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Dept Neurosurg, Los Angeles, CA 90095 USA
[2] Cedars Sinai Med Ctr, Dept Neurosurg, Los Angeles, CA USA
关键词
arteriovenous malformation; molecular biology; vascular biology; ENDOTHELIAL GROWTH-FACTOR; HEREDITARY HEMORRHAGIC TELANGIECTASIA; CENTRAL-NERVOUS-SYSTEM; SMOOTH-MUSCLE-CELLS; RECEPTOR TYROSINE KINASE; SIGNAL-REGULATED KINASE; FOLLOW-UP; MATRIX METALLOPROTEINASES; SPONTANEOUS DISAPPEARANCE; DEVELOPMENTAL EXPRESSION;
D O I
10.3171/2009.2.FOCUS09316
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Object. The scientific understanding of the nature of arteriovenous malformations (AVMs) in the brain is evolving. It is clear from current work that AVMs can undergo a variety of phenomena, including growth, remodeling, and/or regression-and the responsible processes are both molecular and physiological. A review of these complex processes is critical to directing future therapeutic approaches. The authors performed a comprehensive review of the literature to evaluate current information regarding the genetics, pathophysiology, and behavior of AVMs. Methods. A comprehensive literature review was conducted using PubMed to reveal the molecular biology of AVMs as it relates to their complex growth and behavior patterns. Results. Growth factors involved in AVMs include vascular endothelial growth factor, fibroblast growth factor, transforming growth factor beta, angiopoietins, fibronectin, laminin, integrin, and matrix metalloproteinases. Conclusions. Understanding the complicated molecular milieu of developing AVMs is essential for defining their natural history. Growth factors, extracellular matrix proteins, and other molecular markers will be the key to unlocking novel targeted drug treatments for these brain malformations. (DOI: 10.3171/2009.2.FOCUS09316)
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页数:15
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