The Met tyrosine kinase receptor in development and cancer

被引:264
作者
Gentile, Alessandra [1 ]
Trusolino, Livio [1 ]
Comoglio, Paolo M. [1 ]
机构
[1] Univ Turin, Sch Med, Div Mol Oncol, Inst Canc Res & Treatment, I-10060 Turin, Italy
关键词
Met; HGF; tyrosine kinase receptor; metastasis; Invasive growth;
D O I
10.1007/s10555-007-9107-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Met is a tyrosine kinase receptor, encoded by an oncogene, whose crucial role has been elucidated during the last two decades. The complex biological program triggered by Met has been dissected and its biological relevance in both physiology and pathology has been proven. Met supports a morphogenetic program, known as invasive growth, taking place both during embryogenesis and adulthood. In tumors Met is often aberrantly activated, giving rise to the pathological counterpart of the invasive growth program: cancer progression towards metastasis. Several approaches have been recently developed to interfere with the tumorigenic and metastatic processes triggered by Met.
引用
收藏
页码:85 / 94
页数:10
相关论文
共 86 条
[1]   The Met kinase inhibitor SU11274 exhibits a selective inhibition pattern toward different receptor mutated variants [J].
Berthou, S ;
Aebersold, DM ;
Schmidt, LS ;
Stroka, D ;
Heigl, C ;
Streit, B ;
Stalder, D ;
Gruber, G ;
Liang, CX ;
Howlett, AR ;
Candinas, D ;
Greiner, RH ;
Lipson, KE ;
Zimmer, Y .
ONCOGENE, 2004, 23 (31) :5387-5393
[2]   Developmental roles of HGF/SF and its receptor, the c-Met tyrosine kinase [J].
Birchmeier, C ;
Gherardi, E .
TRENDS IN CELL BIOLOGY, 1998, 8 (10) :404-410
[3]   Met, metastasis, motility and more [J].
Birchmeier, C ;
Birchmeier, W ;
Gherardi, E ;
Vande Woude, GF .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2003, 4 (12) :915-925
[4]   ESSENTIAL ROLE FOR THE C-MET RECEPTOR IN THE MIGRATION OF MYOGENIC PRECURSOR CELLS INTO THE LIMB BUD [J].
BLADT, F ;
RIETHMACHER, D ;
ISENMANN, S ;
AGUZZI, A ;
BIRCHMEIER, C .
NATURE, 1995, 376 (6543) :768-771
[5]   Cancer and blood coagulation [J].
Boccaccio, C ;
Medico, E .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2006, 63 (09) :1024-1027
[6]   The MET oncogene drives a genetic programme linking cancer to haemostasis [J].
Boccaccio, C ;
Sabatino, G ;
Medico, E ;
Girolami, F ;
Follenzi, A ;
Reato, G ;
Sottile, A ;
Naldini, L ;
Comoglio, PM .
NATURE, 2005, 434 (7031) :396-400
[7]   Induction of epithelial tubules by growth factor HGF depends on the STAT pathway [J].
Boccaccio, C ;
Andò, M ;
Tamagnone, L ;
Bardelli, A ;
Michieli, P ;
Battistini, C ;
Comoglio, PM .
NATURE, 1998, 391 (6664) :285-288
[8]   IDENTIFICATION OF THE HEPATOCYTE GROWTH-FACTOR RECEPTOR AS THE C-MET PROTOONCOGENE PRODUCT [J].
BOTTARO, DP ;
RUBIN, JS ;
FALETTO, DL ;
CHAN, AML ;
KMIECIK, TE ;
VANDEWOUDE, GF ;
AARONSON, SA .
SCIENCE, 1991, 251 (4995) :802-804
[9]   Fully human monoclonal antibodies to hepatocyte growth factor with therapeutic potential against hepatocyte growth factor/c-Met-dependent human tumors [J].
Burgess, T ;
Coxon, A ;
Meyer, S ;
Sun, J ;
Rex, K ;
Tsuruda, T ;
Chen, Q ;
Ho, SY ;
Li, L ;
Kaufman, S ;
McDorman, K ;
Cattley, RC ;
Sun, JL ;
Elliott, G ;
Zhang, K ;
Feng, X ;
Jia, XC ;
Green, L ;
Radinsky, R ;
Kendall, R .
CANCER RESEARCH, 2006, 66 (03) :1721-1729
[10]   HEPATOCYTE GROWTH-FACTOR IS A POTENT ANGIOGENIC FACTOR WHICH STIMULATES ENDOTHELIAL-CELL MOTILITY AND GROWTH [J].
BUSSOLINO, F ;
DIRENZO, MF ;
ZICHE, M ;
BOCCHIETTO, E ;
OLIVERO, M ;
NALDINI, L ;
GAUDINO, G ;
TAMAGNONE, L ;
COFFER, A ;
COMOGLIO, PM .
JOURNAL OF CELL BIOLOGY, 1992, 119 (03) :629-641