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Original Research

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Expression of E-cadherin in squamous cell carcinomas of the cervix with correlations to clinicopathological features

  • M. Yaldiz1
  • A.U. Hakverdi2,*,
  • G. Bayhan2
  • Z. Akkus3

1Department of Pathology, Turkey

2Department of Obstetrics and Gynecology, Turkey

3Department of Biostatistics, Dicle University, School of Medicine, Diyarbakir, Turkey

DOI: 10.12892/ejgo20050195 Vol.26,Issue 1,January 2005 pp.95-98

Published: 10 January 2005

*Corresponding Author(s): A.U. Hakverdi E-mail:

Abstract

Objective: To evaluate the expression of E-cadherin, a calcium-dependent cell adhesion molecule, in a retrospective analysis of paraffin-embedded tissue specimens of cervical squamous carcinoma and the relationship with histopathological differentiation and lymph node status.

Methods: In this study, we investigated by immunohistochemistry E-cadherin expression in ten normal cervical epithelia and 24 cervical invasive squamous carcinomas.

Results: Normal cervical squamous epithelium showed strong expression of E-cadherin at the membrane of the cell and intercellular junctions. In 24 tumors immunnostained by E-cadherin antibody, 11 (46%) showed preserved expression and 13 (54%) reduced expression. There was no significant correlation between E-cadherin expression and histological differentiation (p = 0.650, p = 0.294). In the status of lymph node metastasis, reduced expression of E-cadherin was seen in 11/15 (73%) with lymph node metastasis versus 2/9 (22%) without lymph node metastasis. There was a significant inverse correlation between E-cadherin expression and lymph node metastasis (p = 0.032).

Conclusion: Reduced E-cadherin expression may be an important factor among a variety of biologic events that occur during the process of metastasis. However, this should be explored by a large scale study.

Keywords

Cervix; Squamous cell carcinoma; E-cadhenn

Cite and Share

M. Yaldiz,A.U. Hakverdi,G. Bayhan,Z. Akkus. Expression of E-cadherin in squamous cell carcinomas of the cervix with correlations to clinicopathological features. European Journal of Gynaecological Oncology. 2005. 26(1);95-98.

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