Forced expression of ΔN-TCF-1B in colon cancer derived cell lines is accompanied by the induction of CEACAM5/6 and mesothelin

被引:18
作者
Liebig, B
Brabletz, T
Staege, MS
Wulfänger, J
Riemann, D
Burdach, S
Ballhausen, WG
机构
[1] Univ Halle Wittenberg, Klin & Poliklin Innere Med 1, Sekt Mol Gastroenterol Onkol, Dept Internal Med 1,Sect Mol GI Oncol, D-06120 Halle Saale, Germany
[2] Univ Erlangen Nurnberg, Dept Pathol, D-8520 Erlangen, Germany
[3] Univ Halle Wittenberg, Dept Paediat, D-06120 Halle Saale, Germany
[4] Univ Halle Wittenberg, Inst Immunol, D-06120 Halle Saale, Germany
[5] Tech Univ Munich, Div Paediat Haematol Oncol, D-8000 Munich, Germany
[6] Tech Univ Munich, Canc Ctr, D-8000 Munich, Germany
关键词
CEACAM; colorectal cancer; high mobility group-box; mesothelin/MPF; T-cell factor; Wnt pathway;
D O I
10.1016/j.canlet.2004.10.013
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The colon cancer cell lines HT29 and SW480 were transfected with an N-terminal beta-catenin binding site-deficient high mobility group (HMG)-box T-cell factor I (Delta N-TCF-1) construct to identify differentially expressed genes. Oligonucleotide HG-U133A microarray expression profiling revealed increased mRNA levels of carcinoembryonic antigen-related cell adhesion molecule (CEACAM) 5, 6 and mesothelin in transfectants positive for nuclear Delta N-TCF-1B. Increased amounts of CEACAM5 (CEA) were detectable in membrane-associated compartments, particularly in cholesterol-enriched microdomains. Similarly, mesothelin was demonstrated as an uncleaved membrane-bound constituent. The identified markers were examined in specimens of 46 colorectal carcinomas (CRC) by immunohistochemistry. Patchy areas of increased CEACAM5/6 staining were seen at the tumour-host front in all samples studied. Twenty-eight (58%) of these cases showed over-expression of mesothelin in a small fraction of tumor cells displaying dedifferentiation and dissemination at the invasion front. We conclude that forced expression of Delta N-TCF-1B in HT29 and SW480 is associated with up-regulation of GPI-anchored adhesion molecules, which were assigned to the tumour-host front in CRC patients. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:159 / 167
页数:9
相关论文
共 22 条
[1]   Convenient and versatile subcellular extraction procedure, that facilitates classical protein expression profiling and functional protein analysis [J].
Abdolzade-Bavil, A ;
Hayes, S ;
Goretzki, L ;
Kröger, M ;
Anders, J ;
Hendriks, R .
PROTEOMICS, 2004, 4 (05) :1397-1405
[2]   Linking colorectal cancer to Wnt signaling [J].
Bienz, M ;
Clevers, H .
CELL, 2000, 103 (02) :311-320
[3]   β-catenin regulates the expression of the matrix metalloproteinase-7 in human colorectal cancer [J].
Brabletz, T ;
Jung, A ;
Dag, S ;
Hlubek, F ;
Kirchner, T .
AMERICAN JOURNAL OF PATHOLOGY, 1999, 155 (04) :1033-1038
[4]   All Tcf HMG box transcription factors interact with Groucho-related co-repressors [J].
Brantjes, H ;
Roose, J ;
van de Wetering, M ;
Clevers, H .
NUCLEIC ACIDS RESEARCH, 2001, 29 (07) :1410-1419
[5]   Molecular cloning of mesothelin, a differentiation antigen present on mesothelium, mesotheliomas, and ovarian cancers [J].
Chang, K ;
Pastan, I .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (01) :136-140
[6]   Large-scale molecular and tissue microarray analysis of mesothelin expression in common human carcinomas [J].
Frierson, HF ;
Moskaluk, CA ;
Powell, SM ;
Zhang, H ;
Cerilli, LA ;
Stoler, MH ;
Cathro, H ;
Hampton, GM .
HUMAN PATHOLOGY, 2003, 34 (06) :605-609
[7]   The Wnt signalling pathway [J].
Huelsken, J ;
Behrens, J .
JOURNAL OF CELL SCIENCE, 2002, 115 (21) :3977-3978
[8]   Deregulated expression of the human tumor marker CEA and CEA family member CEACAM6 disrupts tissue architecture and blocks colonocyte differentiation [J].
Ilantzis, C ;
Demarte, L ;
Screaton, RA ;
Stanners, CP .
NEOPLASIA, 2002, 4 (02) :151-163
[9]   ESTABLISHMENT OF MOUSE-CELL LINES WHICH CONSTITUTIVELY SECRETE LARGE QUANTITIES OF INTERLEUKIN-2, INTERLEUKIN-3, INTERLEUKIN-4 OR INTERLEUKIN-5, USING MODIFIED CDNA EXPRESSION VECTORS [J].
KARASUYAMA, H ;
MELCHERS, F .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1988, 18 (01) :97-104
[10]   BILIARY ADENOCARCINOMA - CHARACTERIZATION OF 3 NEW HUMAN-TUMOR CELL-LINES [J].
KNUTH, A ;
GABBERT, H ;
DIPPOLD, W ;
KLEIN, O ;
SACHSSE, W ;
BITTERSUERMANN, D ;
PRELLWITZ, W ;
ZUMBUSCHENFELDE, KHM .
JOURNAL OF HEPATOLOGY, 1985, 1 (06) :579-596