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No differences in caspase-3 and Bax expression in atrophic-erosive vs. reticular oral lichen planus

Authors :
Antonio Bascones-Martínez
Germán Esparza-Gómez
Julián Campo-Trapero
Cristina Bascones-Ilundain
José Antonio Gil-Montoya
Miguel Ángel González-Moles
Jorge Cano-Sánchez
Source :
Journal of the European Academy of Dermatology and Venereology. :070725185059001
Publication Year :
2007
Publisher :
Wiley, 2007.

Abstract

Background Caspase-3 (CPP32) and Bax expression levels in oral lichen planus (OLP) lesions are considered reliable markers of apoptosis. The malignant transformation of OLP remains a very controversial matter. The objective of this study was to compare histological and apoptotic phenomena between atrophic-erosive and reticular forms of OLP. Methods Analysis was conducted of biopsy samples from 18 patients with reticular and 14 with atrophic-erosive OLP. Conventional histology techniques were used to quantify histological markers of OLP and peroxidase/anti-peroxidase techniques to determine apoptosis markers caspase-3 (CPP32) and Bax. Results More Civatte bodies and lymphocyte exocytosis were observed in atrophic-erosive than reticular OLP samples, without any statistical difference. No statistical significant differences in caspase-3 expression were found between these OLP forms in suprabasal layer (58.3% vs. 43.8%), basal layer (83.3% vs. 68.8%) or infiltrate (69.2% vs. 46.6%). Bax expression was relatively infrequent, and no differences were observed between atrophic-erosive and reticular forms. Conclusions The low frequency of apoptotic phenomena (caspase-3 and Bax) in epithelial cells of OLP may create a favourable substrate for malignant transformation. However, there does not seem to be an association with the clinical form (atrophic-erosive or reticular).

Details

ISSN :
14683083 and 09269959
Database :
OpenAIRE
Journal :
Journal of the European Academy of Dermatology and Venereology
Accession number :
edsair.doi.dedup.....1cd7e734d9b398e877ac91b34f20b1a9
Full Text :
https://doi.org/10.1111/j.1468-3083.2007.02387.x