Activation of c-Met (hepatocyte growth factor receptor) in human gastric cancer tissue

被引:69
作者
Inoue, T
Kataoka, H
Goto, K
Nagaike, K
Igami, K
Naka, D
Kitamura, N
Miyazawa, K [1 ]
机构
[1] Univ Tokyo, Dept Mol Pathol, Grad Sch Med, Tokyo 1130033, Japan
[2] Tokyo Inst Technol, Grad Sch Biosci & Biotechnol, Dept Biol Sci, Yokohama, Kanagawa 2268501, Japan
[3] Miyazaki Med Coll, Dept Pathol 2, Kiyotake, Miyazaki 8891692, Japan
[4] Mitsubishi Chem Co, Yokohama Res Ctr, Yokohama, Kanagawa 2278502, Japan
关键词
D O I
10.1111/j.1349-7006.2004.tb02185.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
c-Met is a high-affinity receptor for hepatocyte growth factor (HGF) and plays a crucial role in embryonic development, as well as in the process of tissue repair. Overexpression and amplification of c-Met are often observed in various cancer tissues, especially in gastric carcinoma. It has, however, been unclear whether the overexpression leads to activation of the c-Met receptor. To address this point, we prepared an antibody (anti-phospho-Met) which specifically recognizes c-Met that is phosphorylated at Y1235, a major phosphorylation site of c-Met. Normal as well as cancerous gastric tissue was positive for anti-total-Met staining, whereas only cancerous tissue was strongly positive for antiphospho-Met staining; cells near the basal layer were moderately positive, and the proliferative zone in normal tissue was only weakly positive. Among cancerous tissues from seven patients examined in the present study, those from six patients were strongly positive for phospho-Met staining. These results indicate that c-Met is actually activated in gastric carcinoma tissue, and may trigger proliferation /anti-apoptotic signals.
引用
收藏
页码:803 / 808
页数:6
相关论文
共 28 条
[1]   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
[2]   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
[3]   Mutations in the met oncogene unveil a "dual switch" mechanism controlling tyrosine kinase activity [J].
Chiara, F ;
Michieli, P ;
Pugliese, L ;
Comoglio, PM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (31) :29352-29358
[4]  
Christensen JG, 2003, CANCER RES, V63, P7345
[5]   Helicobacter pylori CagA protein targets the c-Met receptor and enhances the motogenic response [J].
Churin, Y ;
Al-Ghoul, L ;
Kepp, O ;
Meyer, TE ;
Birchmeier, W ;
Naumann, M .
JOURNAL OF CELL BIOLOGY, 2003, 161 (02) :249-255
[6]   MOLECULAR-CLONING OF A NEW TRANSFORMING GENE FROM A CHEMICALLY TRANSFORMED HUMAN CELL-LINE [J].
COOPER, CS ;
PARK, M ;
BLAIR, DG ;
TAINSKY, MA ;
HUEBNER, K ;
CROCE, CM ;
VANDEWOUDE, GF .
NATURE, 1984, 311 (5981) :29-33
[7]  
Danilkovitch-Miagkova A, 2002, J CLIN INVEST, V109, P863
[8]  
FERRACINI R, 1991, J BIOL CHEM, V266, P19558
[9]   The Semaphorin 4D receptor controls invasive growth by coupling with Met [J].
Giordano, S ;
Corso, S ;
Conrotto, P ;
Artigiani, S ;
Gilestro, G ;
Barberis, D ;
Tamagnone, L ;
Comoglio, PM .
NATURE CELL BIOLOGY, 2002, 4 (09) :720-724
[10]   Autoregulatory mechanisms in protein-tyrosine kinases [J].
Hubbard, SR ;
Mohammadi, M ;
Schlessinger, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (20) :11987-11990