Reverse correlation of E-cadherin and snail expression in oral squamous cell carcinoma cells in vitro

被引:272
作者
Yokoyama, K [1 ]
Kamata, N [1 ]
Hayashi, E [1 ]
Hoteiya, T [1 ]
Ueda, N [1 ]
Fujimoto, R [1 ]
Nagayama, M [1 ]
机构
[1] Univ Tokushima, Sch Dent, Dept Oral & Maxillofacial Surg 1, Tokushima 770, Japan
关键词
SCC; invasion; E-cadherin; catenin; snail;
D O I
10.1016/S1368-8375(00)00059-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
The loss of E-cadherin expression has been shown to correlate to the invasion and metastasis of many types of carcinomas. We established E-cadherin positive (HOC719-PE) and negative (HOC719-NE) clones from an oral squamous cell carcinoma (SCC). HOC719-PE cells showed epithelial morphology with E-cadherin expression in the cell membrane, whereas HOC719-NE cells demonstrated fibroblastic morphology without E-cadherin expression. In invasion assay and three dimensional culture, HOC719-NE showed much higher invasive ability than HOC719-PE cells. These cells expressed similar levels of mRNAs for alpha- and beta -catenin. However, HOC719-NE cells, bur not HOC719-PE cells, showed strong expression of snail, a transcription factor implicated in the differentiation of epithelial cells into mesenchymal phenotype. This reverse expression of snail and E-cadherin was further observed in other SCC cells including HOC313, and TSU cells that we previously reported to show no expression of E-cadherin protein. These results indicated that the expression of snail has a key role for the acquisition of more invasive and metastatic phenotypes of SCC and the clones we reported here will be useful tools for understanding the mechanism of the transition from epithelial to mesenchymal SCC cells. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:65 / 71
页数:7
相关论文
共 40 条
[1]
The transcription factor Snail is a repressor of E-cadherin gene expression in epithelial tumour cells [J].
Batlle, E ;
Sancho, E ;
Franci, C ;
Domínguez, D ;
Monfar, M ;
Baulida, J ;
de Herreros, AG .
NATURE CELL BIOLOGY, 2000, 2 (02) :84-89
[2]
THE E-CADHERIN PROMOTER - FUNCTIONAL-ANALYSIS OF A G.C-RICH REGION AND AN EPITHELIAL CELL-SPECIFIC PALINDROMIC REGULATORY ELEMENT [J].
BEHRENS, J ;
LOWRICK, O ;
KLEINHITPASS, L ;
BIRCHMEIER, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (24) :11495-11499
[3]
LIVING TISSUE FORMED INVITRO AND ACCEPTED AS SKIN-EQUIVALENT TISSUE OF FULL THICKNESS [J].
BELL, E ;
EHRLICH, HP ;
BUTTLE, DJ ;
NAKATSUJI, T .
SCIENCE, 1981, 211 (4486) :1052-1054
[4]
Localization of matrix metalloproteinase MMP-2 to the surface of invasive cells by interaction with integrin alpha v beta 3 [J].
Brooks, PC ;
Stromblad, S ;
Sanders, LC ;
vonSchalscha, TL ;
Aimes, RT ;
StetlerStevenson, WG ;
Quigley, JP ;
Cheresh, DA .
CELL, 1996, 85 (05) :683-693
[5]
TRANSCRIPTIONAL REGULATION OF THE HUMAN E-CADHERIN GENE IN HUMAN PROSTATE-CANCER CELL-LINES - CHARACTERIZATION OF THE HUMAN E-CADHERIN GENE PROMOTER [J].
BUSSEMAKERS, MJG ;
GIROLDI, LA ;
VANBOKHOVEN, A ;
SCHALKEN, JA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 203 (02) :1284-1290
[6]
The transcription factor Snail controls epithelial-mesenchymal transitions by repressing E-cadherin expression [J].
Cano, A ;
Pérez-Moreno, MA ;
Rodrigo, I ;
Locascio, A ;
Blanco, MJ ;
del Barrio, MG ;
Portillo, F ;
Nieto, MA .
NATURE CELL BIOLOGY, 2000, 2 (02) :76-83
[7]
The metalloproteinase matrilysin is a target of β-catenin transactivation in intestinal tumors [J].
Crawford, HC ;
Fingleton, BM ;
Rudolph-Owen, LA ;
Goss, KJH ;
Rubinfeld, B ;
Polakis, P ;
Matrisian, LM .
ONCOGENE, 1999, 18 (18) :2883-2891
[8]
LINEAR ORGANIZATION OF THE LIVER-CELL ADHESION MOLECULE L-CAM [J].
CUNNINGHAM, BA ;
LEUTZINGER, Y ;
GALLIN, WJ ;
SORKIN, BC ;
EDELMAN, GM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (18) :5787-5791
[9]
DOKI Y, 1993, CANCER RES, V53, P3421
[10]
EWING CM, 1995, CANCER RES, V55, P4813