A comparative evaluation of various invasion assays testing colon carcinoma cell lines

被引:32
作者
de Both, NJ
Vermey, M
Dinjens, WN
Bosman, FT
机构
[1] Erasmus Univ, Med Ctr, Dept Pathol, Josephine Nefkens Inst, NL-3000 DR Rotterdam, Netherlands
[2] Univ Lausanne, Dept Pathol, CH-1011 Lausanne, Switzerland
关键词
Matrigel; confluent fibroblast layers; chicken hearts; orthotopic transplantation;
D O I
10.1038/sj.bjc.6690790
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Various colon carcinoma cell lines were tested in different invasion assays, i.e. invasion into Matrigel, into confluent fibroblast layers and into chicken heart tissue. Furthermore, invasive capacity and metastatic potential were determined in nude mice. The colon carcinoma cells used were the human cell lines Caco-2, SW-480, SW-620 and HT-29, and the murine lines Colon-26 and -38. None of the human colon carcinoma cells migrated through porous membranes coated with Matrigel; of the murine lines, only Colon-26 did. When incubated in a mixture of Matrigel and culture medium non-invading cells formed spheroid cultures, whereas invading cells showed a stellate outgrowth. Only the heterogeneously shaped (epithelioid and stellate) cells of SW-480 and SW-620 and the spindle-shaped cells of Colon-26 invaded clearly confluent skin and colon fibroblasts as well as chicken heart tissue. However, when transplanted into the caecum of nude and syngeneic mice, all the lines tested were invasive with the exception of Caco-2 cells. We conclude that the outcome of in vitro tests measuring the invasive capacity of neoplastic cells is largely dependent on the test system used. invasive capacity in vitro is strongly correlated with cells having a spindle cell shape, vimentin expression and E-cadherin down regulation. In contrast, HT-29 and Colon-38 cells having an epithelioid phenotype were clearly invasive and metastatic in vivo, but not in vitro. (C) 1999 Cancer Research Campaign.
引用
收藏
页码:934 / 941
页数:8
相关论文
共 32 条
[1]  
ALBINI A, 1987, CANCER RES, V47, P3239
[2]  
Boyer B, 1996, CURR TOP MICROBIOL, V213, P179
[3]   A NEW ANIMAL-MODEL FOR HUMAN-COLON CANCER METASTASIS [J].
BRESALIER, RS ;
RAPER, SE ;
HUJANEN, ES ;
KIM, YS .
INTERNATIONAL JOURNAL OF CANCER, 1987, 39 (05) :625-630
[4]  
Chao C, 1996, CANCER RES, V56, P4811
[5]  
CORBETT TH, 1975, CANCER RES, V35, P2434
[6]  
DeBoth NJ, 1997, INT J CANCER, V72, P1137, DOI 10.1002/(SICI)1097-0215(19970917)72:6<1137::AID-IJC32>3.0.CO
[7]  
2-Z
[8]   IN-VIVO AND IN-VITRO INVASION IN RELATION TO PHENOTYPIC CHARACTERISTICS OF HUMAN COLORECTAL-CARCINOMA CELLS [J].
DEVRIES, JE ;
DINJENS, WNM ;
DEBRUYNE, GK ;
VERSPAGET, HW ;
VANDERLINDEN, EPM ;
DEBRUINE, AP ;
MAREEL, MM ;
BOSMAN, FT ;
TENKATE, J .
BRITISH JOURNAL OF CANCER, 1995, 71 (02) :271-277
[9]  
EWING CM, 1995, CANCER RES, V55, P4813
[10]   MODULATION OF THE INVASIVE PHENOTYPE OF HUMAN COLON-CARCINOMA CELLS BY ORGAN SPECIFIC FIBROBLASTS OF NUDE-MICE [J].
FABRA, A ;
NAKAJIMA, M ;
BUCANA, CD ;
FIDLER, IJ .
DIFFERENTIATION, 1992, 52 (01) :101-110