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DOI 10.1111/j.1365-2303.2007.00467.x

Медицинская библиотека · Cytopathology : official journal of the British Society for Clinical Cytology · 2007

Altered expression of adhesion molecules in inflammatory cervical smears.

Politi E N, Lazaris A C, Kehriotis M, Papathomas T G, Nikolakopoulou E, Koutselini H

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Аннотация

OBJECTIVE

The aim of the present study was to evaluate the expression of pan-cadherin and beta-catenin in cervical smears with various types of infectious agents.

PATIENTS AND

METHODS

Cervical smears obtained from 53 women, aged 21-65 years, with a diagnosis of specific inflammation were examined in our study. Eighteen subjects were infected by Candida albicans, 18 by Gardnerella vaginalis, nine by Bacteroides spp. and eight by Chlamydia trachomatis. All infectious agents found in the smears were at the same time confirmed by the microbiological laboratory methods. We performed a biotin-streptavidin-peroxidase immunocytochemical method using anti-beta-catenin (Clone 12F7) and anti-pan-cadherin (pan, polyclonal) antibodies.

RESULTS

Aberrant expression of pan-cadherin was found in the cytoplasmic membrane of glandular, metaplastic, superficial and intermediate squamous cells in all types of infections. With regard to beta-catenin, this was expressed in majority (90%) of glandular and metaplastic cells in all types of infections and in a small proportion (15%) of superficial and intermediate squamous cells in infections caused by C. albicans and G. vaginalis.

CONCLUSION

Our data show that infectious agents may cause alterations in the expression and distribution of these adhesive molecules, which can be recognized in cervical smears. Additional studies in larger sets of patients should help clarify this issue further.

Для цитирования: Politi E N, Lazaris A C, Kehriotis M, Papathomas T G, Nikolakopoulou E, Koutselini H. Altered expression of adhesion molecules in inflammatory cervical smears.. Cytopathology : official journal of the British Society for Clinical Cytology. 2007. DOI: 10.1111/j.1365-2303.2007.00467.x.

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