Role of TMPRSS4 During Cancer Progression

被引:22
作者
Choi, So-Young [1 ]
Shin, Hyun-Chul [2 ]
Kim, Seon-Young [3 ]
Park, Young Woo [1 ]
机构
[1] KRIBB, Therapeut Antibody Res Ctr, Taejon 305806, South Korea
[2] Korea Natl Univ Educ, Dept Chem, Physiol & Biochem Lab, Cheongwon, South Korea
[3] KRIBB, Funct Genom Res Ctr, Taejon 305806, South Korea
关键词
D O I
10.1358/dnp.2008.21.8.1272135
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Proteases play important roles in the development and homeostasis of an organism. These versatile proteins participate in a variety of biological processes. In addition to these functions, the importance of proteases as a key player in cancer progression has been increasingly recognized. Proteolysis by dysregulated proteases is one of the hallmarks of cancer progression. In many cancers, a variety of functions have been uncovered for the type 11 transmembrane serine proteases (TTSPs), which are recently discovered members of the family of cell-surface associated proteases. In this review, we describe the characteristics of TTSPs and their role in many human cancers. Among the many TTSPs, we discuss TMPRSS4/MT-SP2 in the greatest detail. TMPRSS4 is upregulated in prostate, colon and gastric cancers, and was recently shown to promote tumor growth, invasion, metastasis and the epithelial-mesenchymal transition (EMT). Currently, efforts are being made to understand the pathways through which TMPRSS4 activates the EMT. Recent studies indicate that the EMT induced by TMPRSS4 involves activation of extracellular signal regulated kinase (ERK) 1/2 and mitogen-activated protein kinase (MAPK). The target molecule for TMPRSS4 that initiates the EMT stimulatory pathway is still not defined. Regulation of the EMT by proteases such as TMPRSS4 may provide novel therapeutic targets for a cancer metastasis inhibitor. (C) 2008 Prous Science, S.A.U. or its licensors. All rights reserved.
引用
收藏
页码:417 / 423
页数:7
相关论文
共 73 条
[51]   A novel biomarker for staging human prostate adenocarcinoma: Overexpression of matriptase with concomitant loss of its inhibitor, hepatocyte growth factor activator inhibitor-1 [J].
Saleem, M ;
Adhami, VM ;
Zhong, WX ;
Longley, BJ ;
Lin, CY ;
Dickson, RB ;
Reagan-Shaw, S ;
Jarrard, DF ;
Mukhtar, H .
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2006, 15 (02) :217-227
[52]   The novel serine protease tumor-associated differentially expressed gene-15 (Matriptase/MT-SP1) is highly overexpressed in cervical carcinoma [J].
Santin, AD ;
Cane, S ;
Bellone, S ;
Bignotti, E ;
Palmieri, M ;
De Las Casas, LE ;
Anfossi, S ;
Roman, JJ ;
O'Brien, T ;
Pecorelli, S .
CANCER, 2003, 98 (09) :1898-1904
[53]   The transmembrane protease serine (TMPRSS3/TADG-12) D variant: A potential candidate for diagnosis and therapeutic intervention in ovarian cancer [J].
Sawasaki, T ;
Shigemasa, K ;
Gu, LJ ;
Beard, JB ;
O'Brien, TJ .
TUMOR BIOLOGY, 2004, 25 (03) :141-148
[54]   SMART, a simple modular architecture research tool: Identification of signaling domains [J].
Schultz, J ;
Milpetz, F ;
Bork, P ;
Ponting, CP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (11) :5857-5864
[55]   Expression of the serine protease Desc1 correlates directly with normal keratinocyte differentiation and inversely with head and neck squamous cell carcinoma progression [J].
Sedghizadeh, PP ;
Mallery, SR ;
Thompson, SJ ;
Kresty, L ;
Beck, FM ;
Parkinson, EK ;
Biancamano, J ;
Lang, JC .
HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK, 2006, 28 (05) :432-440
[56]  
Srikantan V, 2002, CANCER RES, V62, P6812
[57]   Proteases in invasion: matrix metalloproteinases [J].
Stetler-Stevenson, WG ;
Yu, AE .
SEMINARS IN CANCER BIOLOGY, 2001, 11 (02) :143-152
[58]   Apoptotic cues from the extracellular matrix: regulators of angiogenesis [J].
Stupack, DG ;
Cheresh, DA .
ONCOGENE, 2003, 22 (56) :9022-9029
[59]   Epithelial-mesenchymal transformation is the mechanism for fusion of the craniofacial primordia involved in morphogenesis of the chicken lip [J].
Sun, DZ ;
Baur, S ;
Hay, ED .
DEVELOPMENTAL BIOLOGY, 2000, 228 (02) :337-349
[60]   Type II transmembrane serine proteases [J].
Szabo, R ;
Wu, QY ;
Dickson, RB ;
Netzel-Arnett, S ;
Antalis, TM ;
Bugge, TH .
THROMBOSIS AND HAEMOSTASIS, 2003, 90 (02) :185-193