c-Met expression in gastric cancer with liver metastasis

被引:91
作者
Amemiya, H [1 ]
Kono, K [1 ]
Itakura, J [1 ]
Tang, RF [1 ]
Takahashi, A [1 ]
An, FQ [1 ]
Kamei, S [1 ]
Iizuka, H [1 ]
Fujii, H [1 ]
Matsumoto, Y [1 ]
机构
[1] Yamanashi Med Univ, Dept Surg 1, Yamanashi 4093898, Japan
关键词
gastric cancer; stage IV; liver metastasis; c-Met; hepatocyte growth factor; proliferating cell nuclear antigen; prognosis; immunohistochemistry; semiquantitative reverse transcriptase-polymerase; chain reaction;
D O I
10.1159/000065477
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Liver metastasis is one of the poor prognostic factors for gastric cancer. Hepatocyte growth factor (HGF) and its receptor, c-Met, have been reported to be related to the proliferation of carcinoma cells. We examined c-Met and HGF expression in stage IV gastric cancers (n = 121) and compared the results in groups with liver metastasis (n = 47, LM group) and without liver metastasis (n = 74, no-LM group). The survival rate for the LM group was significantly poorer than for the no-LM group (p < 0.01). We found a high frequency of c-Met expression in the LM group compared with the no-LM group at protein level detected by immunohistochemistry (p = 0.0005) and at mRNA level detected by semiquantitative reverse transcriptase-polymerase chain reaction (p = 0.0386) in primary gastric tumors. Furthermore, we evaluated HGF expression in both carcinoma cells and stromal cells in gastric cancers. There was no significant difference in the HGF expression between the LM and noLM groups. The labeling index of proliferating cell nuclear antigen for the carcinomas in the LM group was higher than that in the no-LM group (47.1 +/- 24.5 vs. 26.2 24.5%, p < 0.0001). Thus, the high frequency of c-Met overexpression in carcinoma cells may be involved in the mechanism of liver metastasis in gastric cancers. Moreover, the evaluation of c-Met expression might be a useful indicator of liver metastasis in patients with gastric cancer. Copyright (C) 2002 S. Karger AG, Basel.
引用
收藏
页码:286 / 296
页数:11
相关论文
共 40 条
[21]   Mutant Met-mediated transformation is ligand-dependent and can be inhibited by HGF antagonists [J].
Michieli, P ;
Basilico, C ;
Pennacchietti, S ;
Maffè, A ;
Tamagnone, L ;
Giordano, S ;
Bardelli, A ;
Comoglio, PM .
ONCOGENE, 1999, 18 (37) :5221-5231
[22]   IDENTIFICATION OF A FIBROBLAST-DERIVED EPITHELIAL MORPHOGEN AS HEPATOCYTE GROWTH-FACTOR [J].
MONTESANO, R ;
MATSUMOTO, K ;
NAKAMURA, T ;
ORCI, L .
CELL, 1991, 67 (05) :901-908
[23]  
MORI M, 1993, SURGERY, V113, P683
[24]   PURIFICATION AND SUBUNIT STRUCTURE OF HEPATOCYTE GROWTH-FACTOR FROM RAT PLATELETS [J].
NAKAMURA, T ;
NAWA, K ;
ICHIHARA, A ;
KAISE, N ;
NISHINO, T .
FEBS LETTERS, 1987, 224 (02) :311-316
[25]   PARTIAL-PURIFICATION AND CHARACTERIZATION OF HEPATOCYTE GROWTH-FACTOR FROM SERUM OF HEPATECTOMIZED RATS [J].
NAKAMURA, T ;
NAWA, K ;
ICHIHARA, A .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1984, 122 (03) :1450-1459
[26]  
Natali PG, 1996, INT J CANCER, V69, P212, DOI 10.1002/(SICI)1097-0215(19960621)69:3<212::AID-IJC11>3.3.CO
[27]  
2-X
[28]   HEPATIC RESECTION FOR METASTATIC TUMORS FROM GASTRIC-CANCER - ANALYSIS OF PROGNOSTIC FACTORS [J].
OCHIAI, T ;
SASAKO, M ;
MIZUNO, S ;
KINOSHITA, T ;
TAKAYAMA, T ;
KOSUGE, T ;
YAMAZAKI, S ;
MARUYAMA, K .
BRITISH JOURNAL OF SURGERY, 1994, 81 (08) :1175-1178
[29]   SEQUENCE OF MET PROTOONCOGENE CDNA HAS FEATURES CHARACTERISTIC OF THE TYROSINE KINASE FAMILY OF GROWTH-FACTOR RECEPTORS [J].
PARK, M ;
DEAN, M ;
KAUL, K ;
BRAUN, MJ ;
GONDA, MA ;
VANDEWOUDE, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (18) :6379-6383
[30]  
PONZETTO C, 1991, ONCOGENE, V6, P553