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PMID: 10541972 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

E-cadherin expression in oesophageal carcinoma treated with high-dose radiotherapy; correlation with pretreatment parameters and treatment outcome.

Journal of cancer research and clinical oncology ·Vol. 125 ·No. 11 ·1999-11-00 ·Pages 641-5

Pomp J, Blom J, van Krimpen C, Zwinderman AH, Immerzeel JJ

Abstract

E-cadherin plays an important role in the cell-cell contact of normal epithelium. Loss of E-cadherin expression may be related to tumour invasiveness and metastatic potential. In a group of patients treated for oesophageal carcinoma by radiotherapy only, we found that immunohistochemically detected p53 expression correlated with reduced survival, mainly because of the occurrence of distant metastases. We questioned whether, in this group of patients, E-cadherin expression was concomitantly altered and served as a predictive factor for the development of distant metastases. Immunostaining for E-cadherin was performed on paraffin- embedded biopsy specimens from patients with adenocarcinoma and squamous cell carcinoma of the oesophagus. E-cadherin status and its correlation with regard to pretreatment parameters and treatment outcome were determined. An aberrant staining pattern of E-cadherin did not correlate with any of the pretreatment parameters. In a univariate analysis, a significantly reduced metastatic potential was found for tumours that had an aberrant cellular staining pattern for E-cadherin, which was strongest for squamous cell carcinomas. However, in a multivariate analysis only p53 status correlated significantly with the occurrence of distant metastases. Although, in univariate analysis, aberrant E-cadherin expression served as a better, rather than a worse prognostic factor, p53 status remained the only significant parameter in multivariate analysis, in this group of patients with oesophageal carcinoma. No relationship between p53 status and E-cadherin expression was found.

MeSH Terms
Adenocarcinoma/metabolism,mortality,radiotherapy Aged Cadherins/biosynthesis Carcinoma, Squamous Cell/metabolism,mortality,radiotherapy Disease-Free Survival Esophageal Neoplasms/metabolism,mortality,radiotherapy Female Follow-Up Studies Humans Immunohistochemistry Male Predictive Value of Tests Survival Rate Treatment Outcome Tumor Suppressor Protein p53/biosynthesis
Chemicals
Cadherins Tumor Suppressor Protein p53
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Pomp J
Department of Radiation Oncology, Reinier de Graaf Group, P.O. Box 5011, 2600 GA, Delft, The Netherlands. POMP@RdGG.nl
Blom J
van Krimpen C
Zwinderman A H
Immerzeel J J
Article Info
Journal
Journal of cancer research and clinical oncology
Abbr.
J Cancer Res Clin Oncol
ISSN
0171-5216
Published
1999-11-00
Pages
641-5
Language
English
Region
Germany
NLM ID
7902060
Subset
IM
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