Abnormal immunoreactivity of the E-cadherin-catenin complex in gastric carcinoma: Relationship with patient survival

被引:240
作者
Jawhari, A
Jordan, S
Poole, S
Browne, P
Pignatelli, M
Farthing, MJG
机构
[1] ST BARTHOLOMEWS HOSP, DEPT MED STAT, LONDON, ENGLAND
[2] ST BARTHOLOMEWS HOSP, DEPT HISTOPATHOL, LONDON, ENGLAND
[3] HAMMERSMITH HOSP, ROYAL POSTGRAD MED SCH, DEPT HISTOPATHOL, LONDON W12 0HS, ENGLAND
关键词
D O I
10.1016/S0016-5085(97)70218-X
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: The E-cadherin-catenin complex plays a critical role in the maintenance of normal tissue architecture, Mutation of any of its components is believed to result in loss of cell-cell adhesion and contribute to neoplasia, The aim of this study was to examine the expression of E-cadherin and alpha-, gamma-, and gamma-catenin ire gastric carcinoma and dysplasia and determine any relationship with tumor characteristics and survival, Methods: Immunoperoxidase staining of E-cadherin and alpha-, beta-, and gamma-catenin was performed using 89 gastric carcinomas, lymph node metastases, and gastric biopsy specimens from 24 patients with dysplasia and 10 healthy controls, Results: Membranous staining was observed in control biopsy specimens for all components of the complex. Up to 57% of gastric dysplasia and 90% of tumors stained abnormally for one or more components of the cadherin-catenin complex, Abnormal E-cadherin and gamma-catenin staining occurred more frequently in diffuse than intestinal tumors (P < 0.0005 and < 0.05, respectively). No association with tumor grade or stage was found, A survival advantage was noted in intestinal and diffuse tumors retaining membranous expression of beta-catenin, independent of tumor type, grade, or stage (P < 0.005), Conclusions: Abnormal expression of the E-cadherin-catenin complex occurs frequently in gastric carcinoma, The close correlation with poor survival suggests that abnormal beta-catenin may be a useful prognostic marker.
引用
收藏
页码:46 / 54
页数:9
相关论文
共 50 条
[1]   EXON SKIPPING IN THE E-CADHERIN GENE TRANSCRIPT IN METASTATIC HUMAN GASTRIC CARCINOMAS [J].
BECKER, KF ;
ATKINSON, MJ ;
REICH, U ;
HUANG, HH ;
NEKARDA, H ;
SIEWERT, JR ;
HOFLER, H .
HUMAN MOLECULAR GENETICS, 1993, 2 (06) :803-804
[2]  
BECKER KF, 1994, CANCER RES, V54, P3845
[3]   LOSS OF EPITHELIAL DIFFERENTIATION AND GAIN OF INVASIVENESS CORRELATES WITH TYROSINE PHOSPHORYLATION OF THE E-CADHERIN BETA-CATENIN COMPLEX IN CELLS TRANSFORMED WITH A TEMPERATURE-SENSITIVE V-SRC GENE [J].
BEHRENS, J ;
VAKAET, L ;
FRIIS, R ;
WINTERHAGER, E ;
VANROY, F ;
MAREEL, MM ;
BIRCHMEIER, W .
JOURNAL OF CELL BIOLOGY, 1993, 120 (03) :757-766
[4]  
BIRCHMEIER W, 1993, SEMIN CANCER BIOL, V4, P231
[5]  
BRINGUIER PP, 1993, CANCER RES, V53, P3241
[6]   DISTINCT CADHERIN CATENIN COMPLEXES IN CA2+-DEPENDENT CELL-CELL ADHESION [J].
BUTZ, S ;
KEMLER, R .
FEBS LETTERS, 1994, 355 (02) :195-200
[7]   IMMUNOHISTOCHEMICAL DEMONSTRATION OF C-ERBB-2 ONCOPROTEIN IN GASTRIC ADENOCARCINOMA - COMPARISON OF CRYOSTAT AND PARAFFIN WAX SECTIONS AND EFFECT OF FIXATION [J].
CHIU, KY ;
LOKE, SL ;
HO, FCS .
JOURNAL OF CLINICAL PATHOLOGY, 1994, 47 (02) :117-121
[8]   PLAKOGLOBIN - A PROTEIN COMMON TO DIFFERENT KINDS OF INTERCELLULAR ADHERING JUNCTIONS [J].
COWIN, P ;
KAPPRELL, HP ;
FRANKE, WW ;
TAMKUN, J ;
HYNES, RO .
CELL, 1986, 46 (07) :1063-1073
[9]   GROWTH-CONTROL FACTORS IN THE GASTROINTESTINAL-TRACT [J].
GOODLAD, RA ;
WRIGHT, NA .
BAILLIERES CLINICAL GASTROENTEROLOGY, 1990, 4 (01) :97-118
[10]   IDENTIFICATION OF A NEURAL ALPHA-CATENIN AS A KEY REGULATOR OF CADHERIN FUNCTION AND MULTICELLULAR ORGANIZATION [J].
HIRANO, S ;
KIMOTO, N ;
SHIMOYAMA, Y ;
HIROHASHI, S ;
TAKEICHI, M .
CELL, 1992, 70 (02) :293-301