Expression of Mad, an antagonist of Myc oncoprotein function, in differentiating keratinocytes during tumorigenesis of the skin

被引:27
作者
Lymboussaki, A
Kaipainen, A
Hatva, E
Vastrik, I
Jeskanen, L
Jalkanen, M
Werner, S
Stenback, F
Alitalo, R
机构
[1] HELSINKI UNIV, TRANSPLANTAT LAB, HELSINKI 00014, FINLAND
[2] HELSINKI UNIV, MOL CANC BIOL LAB, HELSINKI 00014, FINLAND
[3] HELSINKI UNIV, DEPT PATHOL, HELSINKI 00014, FINLAND
[4] TURKU UNIV, TURKU 20520, FINLAND
[5] MAX PLANCK INST BIOCHEM, D-82152 MARTINSRIED, GERMANY
[6] UNIV OULU, DEPT PATHOL, OULU 60220, FINLAND
基金
芬兰科学院;
关键词
Myc oncoprotein; Mad; carcinogenesis; differentiation;
D O I
10.1038/bjc.1996.257
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The Myc oncoprotein is associated with cell proliferation and is often down-regulated during cell differentiation. The related Mad transcription factor, which antagonises Myc activity, is highly expressed in epidermal keratinocytes. Mad also inhibits cell proliferation in vitro. To study Mad expression in keratinocyte proliferation and differentiation; we have analysed Mad RNA expression in regenerating and hyperproliferative epidermal lesions and epidermal tumours of varying degrees of differentiation using the RNA in situ hybridisation and RNAase protection techniques. Mad was strongly expressed in differentiating suprabasal keratinocytes in healing dermal wounds and in benign hyperproliferative conditions, but also in squamous cell carcinomas, in which the keratinocytes retain their differentiation potential. However, Mad expression was lost in palisading basal carcinoma cells and poorly differentiated squamous cell carcinomas, which lacked the epithelial differentiation marker syndecan-1. We therefore suggest that Mad expression is closely associated with epithelial cell differentiation, and that this association is retained in epithelial tumours of the skin.
引用
收藏
页码:1347 / 1355
页数:9
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