Pleiotropic roles of matrix metalloproteinases in tumor angiogenesis: Contrasting, overlapping and compensatory functions

被引:176
作者
Deryugina, Elena I. [1 ]
Quigley, James P. [1 ]
机构
[1] Scripps Res Inst, La Jolla, CA 92037 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2010年 / 1803卷 / 01期
关键词
Cancer; Metastasis; Matrix metalloproteinases; Tumor angiogenesis; Angiogenic switch; VEGF; FGF-2; Neutrophil; MMP-9; ENDOTHELIAL-GROWTH-FACTOR; MARROW-DERIVED CELLS; PLASMINOGEN-ACTIVATOR RECEPTOR; HEPARAN-SULFATE PROTEOGLYCANS; INTEGRIN ALPHA(V) SUBUNIT; BREAST-CANCER CELLS; IN-SITU ZYMOGRAPHY; EXTRACELLULAR-MATRIX; PROGENITOR CELLS; UP-REGULATION;
D O I
10.1016/j.bbamcr.2009.09.017
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A number of extensive reviews are available discussing the roles of MMPs in various aspects of cancer progression from benign tumor formation to overt cancer present with deadly metastases. This review will focus specifically on the evidence functionally linking the MMPs and tumor-induced angiogenesis in various in vivo models. Emphasis has been placed on the cellular origin of the MMPs in tumor tissue, the requirement of proMMIP activation and the resulting proteolytic activity for the induction and progression of tumor angiogenesis. and the pleiotropic roles for some of the MMPs. The functional mechanisms of the angiogenic MMPs are discussed as well as their catalytic detection in complex biological systems. In addition, the contribution of active MMPs to metastatic spread and establishment of secondary metastasis will be discussed in view of the findings indicating that MMPs are involved in the preparation of pre-metastatic niches. Finally, the most recent evidence, indicating the pro-metastatic consequences of anti-angiogenic therapies employing MMP inhibitors will be presented as examples highlighting possible outcomes of interfering with the pleiotropic nature of the MMP functionality. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:103 / 120
页数:18
相关论文
共 241 条
[1]   Matrix metalloproteinase-9 from bone marrow-derived cells contributes to survival but not growth of tumor cells in the lung microenvironment [J].
Acuff, HB ;
Carter, KJ ;
Fingleton, B ;
Gorden, DL ;
Matrisian, LM .
CANCER RESEARCH, 2006, 66 (01) :259-266
[2]   Analysis of host- and tumor-derived proteinases using a custom dual species microarray reveals a protective role for stromal matrix metal loproteinase-12 in non-small cell lung cancer [J].
Acuff, Heath B. ;
Sinnamon, Mark ;
Fingleton, Barbara ;
Boone, Braden ;
Levy, Shawn E. ;
Chen, Xiwu ;
Pozzi, Ambra ;
Carbone, David P. ;
Schwartz, Donald R. ;
Moin, Kamiar ;
Sloane, Bonnie F. ;
Matrisian, Lynn M. .
CANCER RESEARCH, 2006, 66 (16) :7968-7975
[3]   Matrix metalloproteinase-9 is required for tumor vasculogenesis but not for angiogenesis: Role of bone marrow-derived myelomonocytic cells [J].
Ahn, G-One ;
Brown, J. Martin .
CANCER CELL, 2008, 13 (03) :193-205
[4]   Inhibition of angiogenesis and tumor metastasis by targeting a matrix immobilized cryptic extracellular matrix epitope in laminin [J].
Akaht, Abebe ;
Roth, Jennifer M. ;
Caunt, Maresa ;
Policarpio, Desiree ;
Liebes, Leonard ;
Brooks, Peter C. .
CANCER RESEARCH, 2007, 67 (09) :4353-4363
[5]   Human neutrophils uniquely release TIMP-free MMP-9 to provide a potent catalytic stimulator of angiogenesis [J].
Ardi, Veronica C. ;
Kupriyanova, Tatyana A. ;
Deryugina, Elena I. ;
Quigley, James P. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (51) :20262-20267
[6]   Neutrophil MMP-9 Proenzyme, Unencumbered by TIMP-1, Undergoes Efficient Activation in Vivo and Catalytically Induces Angiogenesis via a Basic Fibroblast Growth Factor (FGF-2)/FGFR-2 Pathway [J].
Ardi, Veronica C. ;
Van den Steen, Philippe E. ;
Opdenakker, Ghislain ;
Schweighofer, Bernhard ;
Deryugina, Elena I. ;
Quigley, James P. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (38) :25854-25866
[7]   VEGF contributes to postnatal neovascularization by mobilizing bone marrow-derived endothelial progenitor cells [J].
Asahara, T ;
Takahashi, T ;
Masuda, H ;
Kalka, C ;
Chen, DH ;
Iwaguro, H ;
Inai, Y ;
Silver, M ;
Isner, JM .
EMBO JOURNAL, 1999, 18 (14) :3964-3972
[8]   Loss of collagenase-2 confers increased skin tumor susceptibility to male mice [J].
Balbín, M ;
Fueyo, A ;
Tester, AM ;
Pendás, AM ;
Pitiot, AS ;
Astudillo, A ;
Overall, CM ;
Shapiro, SD ;
López-Otín, C .
NATURE GENETICS, 2003, 35 (03) :252-257
[9]   Analyses of all matrix metalloproteinase members in leukocytes emphasize monocytes as major inflammatory mediators in multiple sclerosis [J].
Bar-Or, A ;
Nuttall, RK ;
Duddy, M ;
Alter, A ;
Kim, HJ ;
Ifergan, I ;
Pennington, CJ ;
Bourgoin, P ;
Edwards, DR ;
Yong, VW .
BRAIN, 2003, 126 :2738-2749
[10]   MT1-MMP controls tumor-induced angiogenesis through the release of semaphorin 4D [J].
Basile, John R. ;
Holmbeck, Kenn ;
Bugge, Thomas H. ;
Gutkind, J. Silvio .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (09) :6899-6905