Roles of Matrix Metalloproteinases and Their Natural Inhibitors in Prostate Cancer Progression

被引:146
作者
Gong, Yixuan [1 ]
Chippada-Venkata, Uma D. [1 ]
Oh, William K. [1 ]
机构
[1] Icahn Sch Med Mt Sinai, Tisch Canc Inst, Div Hematol & Med Oncol, New York, NY 10029 USA
关键词
MMP; TIMP; prostate cancer; PLASMA TISSUE INHIBITOR; IN-SITU HYBRIDIZATION; TUMOR-CELL INVASION; LONG-TERM SURVIVAL; IV COLLAGENASE; GROWTH-FACTOR; ANDROGEN DEPRIVATION; UP-REGULATION; E-CADHERIN; 1-MATRIX METALLOPROTEINASE;
D O I
10.3390/cancers6031298
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Matrix metalloproteinases (MMPs), a group of zinc-dependent endopeptidases involved in the degradation of the extracellular matrix, play an important role in tissue remodeling associated with various physiological processes such as morphogenesis, angiogenesis, and tissue repair, as well as pathological processes including cirrhosis, arthritis and cancer. The MMPs are well established as mediators of tumor invasion and metastasis by breaking down connective tissue barriers. Although there has been a vast amount of literature on the role of MMPs in invasion, metastasis and angiogenesis of various cancers, the role of these endopeptidases in prostate cancer progression has not been systematically reviewed. This overview summarizes findings on the tissue and blood expression of MMPs, their function, regulation and prognostic implication in human prostate cancer, with a focus on MMP-2, -7, -9, MT1-MMP and tissue inhibitor of metalloproteinase 1 (TIMP-1). This review also summarizes the efficacy and failure of early-generation matrix metalloproteinase inhibitors (MMPIs) in the treatment of metastatic prostate cancer and highlights the lessons and challenges for next generation MMPIs.
引用
收藏
页码:1298 / 1327
页数:30
相关论文
共 167 条
[1]   Gene expression of angiogenic factors correlates with metastatic potential of prostate cancer cells [J].
Aalinkeel, R ;
Nair, MPN ;
Sufrin, G ;
Mahajan, SA ;
Chadha, KC ;
Chawda, RP ;
Schwartz, SA .
CANCER RESEARCH, 2004, 64 (15) :5311-5321
[2]   Overexpression of MMP-9 Contributes to Invasiveness of Prostate Cancer Cell Line LNCaP [J].
Aalinkeel, Ravikumar ;
Nair, Bindukumar B. ;
Reynolds, Jessica L. ;
Sykes, Donald E. ;
Mahajan, Supriya D. ;
Chadha, Kailash C. ;
Schwartz, Stanley A. .
IMMUNOLOGICAL INVESTIGATIONS, 2011, 40 (05) :447-464
[3]   High Plasma TIMP-1 and Serum CEA Levels during Combination Chemotherapy for Metastatic Colorectal Cancer Are Significantly Associated with Poor Outcome [J].
Aldulaymi, Bahir ;
Bystrom, Per ;
Berglund, Ake ;
Christensen, Ib J. ;
Brunner, Nils ;
Nielsen, Hans J. ;
Glimelius, Bengt .
ONCOLOGY, 2010, 79 (1-2) :144-149
[4]  
[Anonymous], BONE MARROW RES
[5]  
[Anonymous], MOL CANC
[6]   Membrane type 1 matrix metalloprotease cleaves laminin-10 and promotes prostate cancer cell migration [J].
Bair, EL ;
Chen, ML ;
McDaniel, K ;
Sekiguchi, K ;
Cress, AE ;
Nagle, RB ;
Bowden, GT .
NEOPLASIA, 2005, 7 (04) :380-389
[7]   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
[8]  
Bellmunt Joaquim, 2010, Ther Adv Med Oncol, V2, P189, DOI 10.1177/1758834009359769
[9]   Matrix metalloproteinase-9 triggers the angiogenic switch during carcinogenesis [J].
Bergers, G ;
Brekken, R ;
McMahon, G ;
Vu, TH ;
Itoh, T ;
Tamaki, K ;
Tanzawa, K ;
Thorpe, P ;
Itohara, S ;
Werb, Z ;
Hanahan, D .
NATURE CELL BIOLOGY, 2000, 2 (10) :737-744
[10]   TIMP-1 overexpression promotes tumorigenesis of MDA-MB-231 breast cancer cells and alters expression of a subset of cancer promoting genes in vivo distinct from those observed in vitro [J].
Bigelow, Rebecca L. H. ;
Williams, Briana J. ;
Carroll, Jennifer L. ;
Daves, Lisa K. ;
Cardelli, James A. .
BREAST CANCER RESEARCH AND TREATMENT, 2009, 117 (01) :31-44