Elevated Expression of Matrix Metalloproteinase-9 not Matrix Metalloproteinase-2 Contributes to Progression of Extracranial Arteriovenous Malformation

被引:0
作者
Ting Wei
Haihong Zhang
Neslihan Cetin
Emily Miller
Teri Moak
James Y. Suen
Gresham T. Richter
机构
[1] Center for Investigation of Congenital Anomalies of Vascular Development,Department of Pathology
[2] Arkansas Vascular Biology Program,Department of Otolaryngology
[3] Arkansas Children’s Hospital,Head and Neck Surgery
[4] University of Arkansas for Medical Sciences,Division of Pediatric Otolaryngology
[5] Arkansas Children’s Hospital,undefined
[6] University of Arkansas for Medical Sciences,undefined
[7] University of Arkansas,undefined
[8] University of Arkansas for Medical Sciences,undefined
[9] University of Arkansas for Medical Sciences,undefined
[10] Arkansas Children’s Hospital,undefined
来源
Scientific Reports | / 6卷
关键词
D O I
暂无
中图分类号
学科分类号
摘要
Extracranial arteriovenous malformations (AVMs) are rare but dangerous congenital lesions arising from direct arterial-venous shunts without intervening capillaries. Progressive infiltration, expansion and soft tissue destruction lead to bleeding, pain, debilitation and disfigurement. The pathophysiology of AVMs is not well understood. Matrix Metalloproteinases (MMPs) are thought to play an important role in pathologic processes underlying many diseases. This study investigates the expression of MMP-9 and MMP-2 in aggressive extracranial AVMs. The differential expression of MMP-9 and its regulatory factors is also examined. Herein we demonstrate that mRNA and protein expressions of MMP-9, but not MMP-2, are significantly higher in AVM tissues compared to normal tissues. The serum level of MMP-9, but not MMP-2, is also elevated in AVM patients compared to healthy controls. MMP-9/neutrophil gelatinase-associated lipocalin (NGAL) complex is also significantly increased in AVM tissues. The MMP-9/ tissue inhibitor of metalloproteases-1 (TIMP-1) complex presents as a major form detected in normal tissues. The increased and aberrant expression of MMP-9 and specific MMP-9 forms may help explain the constitutive vascular remodeling and infiltrative nature of these lesions. Specific MMP-9 inhibitors would be a promising treatment for AVMs.
引用
收藏
相关论文
共 79 条
[1]  
Richter GT(2011)Pediatric extracranial arteriovenous malformations Curr Opin Otolaryngol Head Neck Surg. 19 455-461
[2]  
Suen JY(2010)Extracranial arteriovenous malformations: natural progression and recurrence after treatment Plast Reconstr Surg. 125 1185-1194
[3]  
Liu AS(2012)The relationship between the MMP system, adrenoceptors and phosphoprotein phosphatases Br J Pharmacol. 166 1225-1243
[4]  
Mulliken JB(2011)Small molecule anti-cancer compounds selectively target the hemopexin domain of matrix metalloproteinase-9 Cancer Res. 71 4977-4988
[5]  
Zurakowski D(2010)P38 mitogen-activated protein kinase-driven MAPKAPK2 regulates invasion of bladder cancer by modulation of MMP2 and MMP9 activity Cancer Res. 70 832-841
[6]  
Fishman SJ(2005)Increased expression of urinary matrix metalloproteinases parallels the extent and activity of vascular anomalies Pediatrics. 116 38-45
[7]  
Greene AK(2006)Chemically modified tetracyclines (CMT-3 and CMT-8) enable control of the pathologic remodellation of human aortic valve stenosis via MMP9 and VEGF inhibition Int J Cardiol. 111 358-364
[8]  
Rietz A(2006)Destroglycan is selectively cleaved at the parenchymal basement membrane at sites of leukocyte extravasation in experimental autoimmune encephalomyelitis J Exp Med. 203 1007-1019
[9]  
Spiers J(1996)Progelatinase B forms from human neutrophils: complex formation of monomer/Lipocalin with TIMP1 Biol Chem. 377 529-533
[10]  
Defour A(2001)The high molecular weight urinary matrix metalloproteinase (MMP) activity is a complex of Gelatinase B/MMP9 and Neutrophil Gelatinase-associated Lipocalin (NGAL). Modulation of MMP-9 activity by NGAL J Bio Chem. 276 37258-37265