Clinical significance of c-met oncogene alterations in human colorectal cancer

被引:56
作者
Umeki, K [1 ]
Shiota, G [1 ]
Kawasaki, H [1 ]
机构
[1] Tottori Univ, Sch Med, Dept Internal Med 2, Yonago, Tottori 683, Japan
关键词
c-met oncogene; amplification; overexpression; colorectal cancer;
D O I
10.1159/000011985
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Abnormalities of the c-met oncogene have been studied in cancers of many organs including thyroid, lung, pancreas, and stomach. However, little is known about the clinical significance of c-met oncogene abnormalities in colorectal cancer. We investigated the amplification and overexpression of the c-met gene in surgically resected samples from 43 patients with colorectal cancer using Southern blot analysis and reverse transcription-polymerase chain reaction (RT-PCR). Four of 33 (12%) samples of colorectal cancer showed amplification of the c-met gene. Twelve of 43 (30%) exhibited overexpression of the c-met gene. The patients with c-met overexpression showed greater tumor size, compared to those without c-met overexpression (p < 0.05). However, there were no differences in clinical stage, histological differentiation, tumor markers, or overall survival between two groups. The findings of the present study suggest that overexpression of c-met gene plays an important role in growth of colorectal cancer.
引用
收藏
页码:314 / 321
页数:8
相关论文
共 30 条
[1]   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
[2]   MUTATION IN THE DNA MISMATCH REPAIR GENE HOMOLOG HMLH1 IS ASSOCIATED WITH HEREDITARY NONPOLYPOSIS COLON-CANCER [J].
BRONNER, CE ;
BAKER, SM ;
MORRISON, PT ;
WARREN, G ;
SMITH, LG ;
LESCOE, MK ;
KANE, M ;
EARABINO, C ;
LIPFORD, J ;
LINDBLOM, A ;
TANNERGARD, P ;
BOLLAG, RJ ;
GODWIN, AR ;
WARD, DC ;
NORDENSKJOLD, M ;
FISHEL, R ;
KOLODNER, R ;
LISKAY, RM .
NATURE, 1994, 368 (6468) :258-261
[3]  
CHAN AML, 1988, ONCOGENE, V2, P593
[4]   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
[5]   OVEREXPRESSION OF THE C-MET/HGF RECEPTOR IN HUMAN THYROID CARCINOMAS DERIVED FROM THE FOLLICULAR EPITHELIUM [J].
DIRENZO, MF ;
OLIVERO, M ;
SERINI, G ;
ORLANDI, F ;
PILOTTI, S ;
BELFIORE, A ;
COSTANTINO, A ;
VIGNERI, R ;
ANGELI, A ;
PIEROTTI, MA ;
COMOGLIO, PM .
JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 1995, 18 (02) :134-139
[6]  
DIRENZO MF, 1991, ONCOGENE, V6, P1997
[7]  
DIRENZO MF, 1995, CANCER RES, V55, P1129
[8]  
DIRENZO MF, 1995, CLIN CANCER RES, V1, P147
[9]   The classification of cancer of the rectum [J].
Dukes, CE .
JOURNAL OF PATHOLOGY AND BACTERIOLOGY, 1932, 35 (03) :323-332
[10]   THE HUMAN MUTATOR GENE HOMOLOG MSH2 AND ITS ASSOCIATION WITH HEREDITARY NONPOLYPOSIS COLON-CANCER [J].
FISHEL, R ;
LESCOE, MK ;
RAO, MRS ;
COPELAND, NG ;
JENKINS, NA ;
GARBER, J ;
KANE, M ;
KOLODNER, R .
CELL, 1993, 75 (05) :1027-1038