Hostname: page-component-cd9895bd7-p9bg8 Total loading time: 0 Render date: 2024-12-21T14:00:10.911Z Has data issue: false hasContentIssue false

muc-1 gene expression in head and neck squamous cell carcinomas

Published online by Cambridge University Press:  08 March 2006

J. S. Rubin
Affiliation:
Institute of Laryngology and Otology, Royal National Throat Nose and Ear Hospital, London
B. K. Bloor
Affiliation:
Department of Oral Medicine and Pathology, Guy’s, King’s and St Thomas’ School of Medicine and Dentistry, Guy’s Hospital, London
I. R. Hart
Affiliation:
Richard Dimbleby Department of Cancer Research/CRF Laboratory at St Thomas’ Hospital, London
P. R. Morgan
Affiliation:
Department of Oral Medicine and Pathology, Guy’s, King’s and St Thomas’ School of Medicine and Dentistry, Guy’s Hospital, London

Abstract

Polymorphic epithelial mucin (PEM), the protein product of the gene muc-1, is a surface glycoprotein that is produced by a range of normal epithelial cells, but has been shown to be expressed at high levels in a range of adenocarcinomas. It has not been investigated extensively in head and neck related tissues, and not at all in head and neck squamous cell carcinomas (HNSCC). This immunohistochemical investigation using two monoclonal antibodies to muc-1 represents a baseline study of 18 HNSCC. In 13 cases, the glycoprotein was expressed at varying levels, usually in keratinizing foci. Although less prominent, expression was also present to some degree in nine of 23 control specimens of non-neoplastic mucosa, mostly at an epithelial level early in the parakeratinization process. Both antibodies showed a pattern of staining. The cellular basis for muc-1 expression is speculative at present and although it is at a lower level than in adenocarcinomas, it may help to provide further insight into epithelial cell differentiation in squamous cell carcinomas.

Type
Research Article
Copyright
Royal Society of Medicine Press Limited 2000

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)