HGF: a multifunctional growth factor controling cell scattering

被引:127
作者
Stella, MC [1 ]
Comoglio, PM [1 ]
机构
[1] Univ Turin, Sch Med, IRCC, Canc Res Inst, I-10060 Turin, Italy
关键词
HGF/SF; growth factor; signal transduction;
D O I
10.1016/S1357-2725(99)00089-8
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
Hepatocyte Growth Factor, also known as Scatter Factor, is a polypeptide that shows structural homology with enzymes of the blood coagulation cascade. It is a biologically inactive single chain precursor that is then cleaved by specific serine proteases to a fully active alpha beta heterodimer. All the biological responses induced by HGF/SF are elicited by binding to its receptor, a transmembrane tyrosine kinase encoded by the MET proto-oncogene. The signaling cascade triggered by HGF begins with the autophosphorylation of the receptor and is mediated by concomitant activation of different cytoplasmic effecters that bind to the same multifunctional docking site. During development, HGF function is essential: knock-out mice for both ligand and receptor show an embryonic lethal phenotype. HGF/SF displays a unique feature in inducing "branching morphogenesis", a complex program of proliferation and motogenesis in a number of different cell types. Moreover, HGF is involved in the invasive behaviour of several tumor cells both in vivo and in vitro. The role of HGF as putative therapeutical agent in pathologies characterized by massive cell loss or deregulated cell proliferation is under investigation. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1357 / 1362
页数:6
相关论文
共 18 条
[1]  
BARDELLI A, 1997, BIOCHIM BIOPHYS ACTA, V133, P41
[2]  
Chirgadze DY, 1999, NAT STRUCT BIOL, V6, P72
[3]   A point mutation in the MET oncogene abrogates metastasis without affecting transformation [J].
Giordano, S ;
Bardelli, A ;
Zhen, Z ;
Menard, S ;
Ponzetto, C ;
Comoglio, PM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (25) :13868-13872
[4]   A FUNCTIONAL DOMAIN IN THE HEAVY-CHAIN OF SCATTER FACTOR HEPATOCYTE GROWTH-FACTOR BINDS THE C-MET RECEPTOR AND INDUCES CELL-DISSOCIATION BUT NOT MITOGENESIS [J].
HARTMANN, G ;
NALDINI, L ;
WEIDNER, KM ;
SACHS, M ;
VIGNA, E ;
COMOGLIO, PM ;
BIRCHMEIER, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (23) :11574-11578
[5]   HEPATOCYTE GROWTH-FACTOR PREVENTS ACUTE-RENAL-FAILURE AND ACCELERATES RENAL REGENERATION IN MICE [J].
KAWAIDA, K ;
MATSUMOTO, K ;
SHIMAZU, H ;
NAKAMURA, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (10) :4357-4361
[6]   STRUCTURE-FUNCTION ANALYSIS OF HEPATOCYTE GROWTH-FACTOR - IDENTIFICATION OF VARIANTS THAT LACK MITOGENIC ACTIVITY YET RETAIN HIGH-AFFINITY RECEPTOR-BINDING [J].
LOKKER, NA ;
MARK, MR ;
LUIS, EA ;
BENNETT, GL ;
ROBBINS, KA ;
BAKER, JB ;
GODOWSKI, PJ .
EMBO JOURNAL, 1992, 11 (07) :2503-2510
[7]   Uncoupling of Grb2 from the Met receptor in vivo reveals complex roles in muscle development [J].
Maina, F ;
Casagranda, F ;
Audero, E ;
Simeone, A ;
Comoglio, PM ;
Klein, R ;
Ponzetto, C .
CELL, 1996, 87 (03) :531-542
[8]   MOLECULAR-CLONING AND EXPRESSION OF HUMAN HEPATOCYTE GROWTH-FACTOR [J].
NAKAMURA, T ;
NISHIZAWA, T ;
HAGIYA, M ;
SEKI, T ;
SHIMONISHI, M ;
SUGIMURA, A ;
TASHIRO, K ;
SHIMIZU, S .
NATURE, 1989, 342 (6248) :440-443
[9]   SCATTER FACTOR AND HEPATOCYTE GROWTH-FACTOR ARE INDISTINGUISHABLE LIGANDS FOR THE MET RECEPTOR [J].
NALDINI, L ;
WEIDNER, KM ;
VIGNA, E ;
GAUDINO, G ;
BARDELLI, A ;
PONZETTO, C ;
NARSIMHAN, RP ;
HARTMANN, G ;
ZARNEGAR, R ;
MICHALOPOULOS, GK ;
BIRCHMEIER, W ;
COMOGLIO, PM .
EMBO JOURNAL, 1991, 10 (10) :2867-2878
[10]   A MULTIFUNCTIONAL DOCKING SITE MEDIATES SIGNALING AND TRANSFORMATION BY THE HEPATOCYTE GROWTH-FACTOR SCATTER FACTOR-RECEPTOR FAMILY [J].
PONZETTO, C ;
BARDELLI, A ;
ZHEN, Z ;
MAINA, F ;
DALLAZONCA, P ;
GIORDANO, S ;
GRAZIANI, A ;
PANAYOTOU, G ;
COMOGLIO, PM .
CELL, 1994, 77 (02) :261-271