A new in vitro model for analyzing the biological behavior of well-differentiated squamous cell carcinoma

被引:7
|
作者
Satoh, S
Toda, S
Inokuchi, A
Sugihara, H
机构
[1] Saga Univ, Fac Med, Dept Otolaryngol Head & Neck Surg, Saga 8498501, Japan
[2] Saga Univ, Fac Med, Dept Pathol & Biodefense, Div Cellular & Mol Pathol, Saga 8498501, Japan
关键词
squamous cell carcinoma; proliferation; differentiation; invasion; cancer-stromal cell interaction;
D O I
10.1016/j.prp.2004.09.015
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
A suitable model analyzing the behavior of well-differentiated squamous cell carcinoma has not yet been established. We tried to establish such a system using a reconstructed oral mucosa, in which T3M-1 squamous cell carcinoma cells were cultured on 3T3 fibroblast-containing collagen gel. Fibroblasts promoted the stratification and keratinization of T3M-1 cells. During growth, the Ki-67 index of T3M-1 cells with fibroblasts was higher than that of T3M-1 cells alone. Fibroblasts increased the expression of involucrin, a differentiating marker of keratinocytes, in T3M-1 cells. They also promoted the invasion of T3M-1 cells into the gel. When T3M-1 cells alone were cultured in a fibroblast-conditioned (FC) medium, the fibroblast-induced phenomena mentioned above were almost replicated. In addition, epidermal growth factor (EGF) promoted T3M-1 cells growth, but not the invasion. cDNA microarray analysis showed that FC medium increased the expression of EGF receptor and several other mRNAs of T3M-1 cells. The data suggest that T3M-1 cells, under cancer-stromal fibroblast interaction, undergo invasive growth with their well-differentiated squamous phenotype, and that this interaction may be mediated partly by soluble molecules (e.g., EGF) in an autocrine or paracrine pathway. Our system will probably provide a useful model for analyzing the biological behavior of well-differentiated squamous cell carcinoma. (c) 2004 Elsevier GmbH. All rights reserved.
引用
收藏
页码:27 / 35
页数:9
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