Progressive loss of PAX9 expression correlates with increasing malignancy of dysplastic and cancerous epithelium of the human oesophagus

被引:63
作者
Gerber, JK
Richter, T
Kremmer, E
Adamski, J
Höfler, H
Balling, R
Peters, H [1 ]
机构
[1] Univ Newcastle Upon Tyne, Int Ctr Life, Inst Human Genet, Newcastle Upon Tyne NE1 3BZ, Tyne & Wear, England
[2] GSF, Natl Res Ctr Environm & Hlth, Inst Expt Genet, Neuherberg, Germany
[3] Tech Univ Munich, Inst Pathol, D-8000 Munich, Germany
[4] GSF, Natl Res Ctr Environm & Hlth, Inst Mol Immunol, Munich, Germany
[5] GSF, Natl Res Ctr Environm & Hlth, Inst Pathol, Neuherberg, Germany
[6] GSF, Natl Res Ctr Environm & Hlth, Inst Mammalian Genet, Neuherberg, Germany
关键词
PAX9; oesophagus; epithelium; dysplasia; carcinoma;
D O I
10.1002/path.1115
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Pax genes encode a family of transcription factors that play key roles in embryonic development. Whereas the functions of Pax genes in the adult organism are largely unknown, upregulated Pax gene expression has been implicated in tumourigenesis. In this study, PAX9-specific monoclonal antibodies have been generated and it has been shown that PAX9 protein is expressed in the normal epithelium of the adult human oesophagus. PAX9 expression was either lost or significantly reduced in the majority of invasive carcinomas and epithelial dysplasias, the latter representing precancerous lesions. Notably, the percentage of PAX9-positive cells within the epithelium decreased with increasing malignancy of the epithelial lesion. These results identify PAX9 as a sensitive marker for deregulated differentiation of oesophageal keratinocytes and indicate a role for PAX9 in the normal differentiation process of internal stratified squamous epithelia. These data suggest that upregulated PAX9 expression is not required for the formation of the majority of squamous cell carcinomas of the human oesophagus. Copyright (C) 2002 John Wiley Sons, Ltd.
引用
收藏
页码:293 / 297
页数:5
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