Metallothionein expression correlates with metastatic and proliferative potential in squamous cell carcinoma of the oesophagus

被引:58
作者
Hishikawa, Y [1 ]
Koji, T
Dhar, DK
Kinugasa, S
Yamaguchi, M
Nagasue, N
机构
[1] Shimane Med Univ, Dept Surg 2, Izumo, Shimane 6938501, Japan
[2] Nagasaki Univ, Sch Med, Dept Histol & Cell Biol, Nagasaki 8528523, Japan
关键词
metallothionein; in situ hybridization; oesophageal cancer; metastasis; cell proliferation;
D O I
10.1038/sj.bjc.6690753
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The goal of this study is to clarify whether the expression of metallothionein (MT) could affect the prognosis and the metastatic potential of squamous cell carcinoma (SCC) of the oesophagus. In paraffin-embedded specimens resected from 57 patients, MT mRNA and protein expressions were detected by in situ hybridization and immunohistochemistry respectively. The expression of MT was evaluated in respect of clinicopathologic variables and patients' survival. MT mRNA expression was significantly associated with the proportion of lymph node metastasis (71% in MT mRNA-positive tumours vs 42% in MT mRNA-negative tumours; P = 0.0343) and that of distant metastasis (29% in MT mRNA-positive tumours vs 5% in MT mRNA-negative tumours; P = 0.0452), In respect of MT protein expression, the frequency of distant metastasis was more common in MT-positive tumours than in MT-negative tumours (30% in MT-positive tumours vs 8% in MT-negative tumours; P = 0.0446). The survival rate of the patients with MT protein-negative tumours was significantly better than that of the patients with MT protein-positive tumours (P = 0.0340). There was a positive correlation between the expression of MT protein and that of proliferating cell nuclear antigen (P = 0.0018). Therefore, we conclude that MT expression, both at the mRNA and protein levels, may be a potential marker predicting metastatic and proliferative activities of oesophageal SCC. (C) 1999 Cancer Research Campaign.
引用
收藏
页码:712 / 720
页数:9
相关论文
共 52 条
[1]  
AbdelMageed AB, 1997, CANCER GENE THER, V4, P199
[3]  
ALSHENEBER IF, 1993, CANCER, V71, P1954, DOI 10.1002/1097-0142(19930315)71:6<1954::AID-CNCR2820710605>3.0.CO
[4]  
2-#
[5]  
CHIN JL, 1993, CANCER, V72, P3029, DOI 10.1002/1097-0142(19931115)72:10<3029::AID-CNCR2820721027>3.0.CO
[6]  
2-6
[7]   THE C-FOS PROTEIN INTERACTS WITH C-JUN/AP-1 TO STIMULATE TRANSCRIPTION OF AP-1 RESPONSIVE GENES [J].
CHIU, R ;
BOYLE, WJ ;
MEEK, J ;
SMEAL, T ;
HUNTER, T ;
KARIN, M .
CELL, 1988, 54 (04) :541-552
[8]   LOCALIZATION OF METALLOTHIONEIN IN BREAST CARCINOMAS - AN IMMUNOHISTOCHEMICAL STUDY [J].
FRESNO, M ;
WU, WY ;
RODRIGUEZ, JM ;
NADJI, M .
VIRCHOWS ARCHIV A-PATHOLOGICAL ANATOMY AND HISTOPATHOLOGY, 1993, 423 (03) :215-219
[9]   METALLOTHIONEIN EXPRESSION IN HUMAN BREAST-CANCER [J].
GOULDING, H ;
JASANI, B ;
PEREIRA, H ;
REID, A ;
GALEA, M ;
BELL, JA ;
ELSTON, CW ;
ROBERTSON, JF ;
BLAMEY, RW ;
NICHOLSON, RA ;
SCHMID, KW ;
ELLIS, IO .
BRITISH JOURNAL OF CANCER, 1995, 72 (04) :968-972
[10]   Effect of metallothioneins on transformation of gelatinase A from human fibroblast WI-38 cells [J].
Haga, A ;
Nagase, H ;
Kito, H ;
Sato, T .
CANCER LETTERS, 1996, 105 (02) :175-180