Immunohistochemical analysis of the biological potential of odontogenic keratocysts
Language English Country Denmark Media print
Document type Comparative Study, Journal Article
PubMed
16430736
DOI
10.1111/j.1600-0714.2006.00382.x
PII: JOP382
Knihovny.cz E-resources
- MeSH
- Ki-67 Antigen analysis MeSH
- Apoptosis physiology MeSH
- Biomarkers analysis MeSH
- Biology MeSH
- Dentigerous Cyst chemistry pathology MeSH
- Diagnosis, Differential MeSH
- Epithelium chemistry pathology MeSH
- Immunophenotyping MeSH
- Immunohistochemistry MeSH
- Cyclin-Dependent Kinase Inhibitor p27 analysis MeSH
- Protein Kinase Inhibitors analysis MeSH
- Humans MeSH
- Odontogenic Cysts chemistry pathology MeSH
- Prognosis MeSH
- Cell Proliferation MeSH
- Cell Cycle Proteins analysis MeSH
- Apoptosis Regulatory Proteins analysis MeSH
- Proto-Oncogene Proteins c-bcl-2 analysis MeSH
- Radicular Cyst chemistry pathology MeSH
- Receptor, ErbB-2 analysis MeSH
- Basal Cell Nevus Syndrome metabolism pathology MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Comparative Study MeSH
- Names of Substances
- Ki-67 Antigen MeSH
- Biomarkers MeSH
- Cyclin-Dependent Kinase Inhibitor p27 MeSH
- Protein Kinase Inhibitors MeSH
- Cell Cycle Proteins MeSH
- Apoptosis Regulatory Proteins MeSH
- Proto-Oncogene Proteins c-bcl-2 MeSH
- Receptor, ErbB-2 MeSH
BACKGROUND: The aim of this study was to analyse the usefulness of detecting important apoptosis and proliferation markers in assessing the biological potential of odontogenic keratocysts (OKC) and thus selecting the optimal diagnostic algorithm for these lesions. METHODS: Indirect immunohistochemistry and relevant statistical methods were used for analysis of formalin-fixed and paraffin-embedded samples from 98 patients. RESULTS: Nevoid basal cell carcinoma syndrome (NBCCS) keratocysts were characterized by higher expression of Bcl-2, p27Kip1 and c-erbB-2 as well as by lower proliferative activity measured by Ki-67 in basal cell epithelium and by a lower inflammatory response in comparison with sporadic keratocysts. Dentigerous, radicular and non-specified odontogenic cysts differed from both NBCCS and sporadic keratocysts in a wide spectrum of apoptosis and/or cell cycle-related protein expressions, higher proliferation in the basal cell layer, and vice versa, lower proliferation in the suprabasal cell layer. CONCLUSIONS: The NBCCS keratocysts have a different immunophenotype from sporadic keratocysts and both types are distinguishable from dentigerous, radicular and non-specified odontogenic cysts. These findings confirm the separate biological potential of these lesions and the results of the immunohistochemical analysis have diagnostic and prognostic implications.
References provided by Crossref.org
Gorlin-Goltz syndrome with familial manifestation