Expression of Bcl-2 and epithelial growth factor receptor proteins in keratocystic odontogenic tumor in comparison with dentigerous cyst and ameloblastoma
Abstract
Background: Keratocystic odontogenic tumor (KCOT) is a developmental odontogenic cyst on
which various investigations have been focused due to its biological activities, high tendency to recur
and different growth mechanisms in comparison with other cystic lesions. Previous studies have
shown different biological and proliferative activities for the lining epithelium of KCOT. The aim
of this study was immunohistochemical evaluation of Bcl-2 and epidermal growth factor receptor
(EGFR) expression in KCOT compared with dentigerous cyst and ameloblastoma.
Materials and Methods: Formalin-fi xed and paraffi n-embedded tissue sections of 16 cases of
KCOT, 16 cases of dentigerous cyst and 16 cases of ameloblastoma were immunohistochemically
analyzed to determine Bcl-2 and EGFR proteins’ expression. Biotin-Stereotavidin method was used.
It was observed by two oral pathologists separately, and the data were analyzed by Mann–Whitney
and Kruskul–Wallis. P < 0.05 was considered as signifi cant.
Results: Regardless of staining intensity, all cases of ameloblastoma and KCOT except dentigerous
cases were positively stained for Bcl-2. Expression of Bcl-2 was higher in the peripheral layer of
ameloblastoma and basal layer of KCOT. Furthermore, all cases of ameloblastoma and dentigerous
cysts except KCOT samples were positively stained for EGFR. Expression of EGFR was higher in
the peripheral layer of ameloblastoma and basal layer of dentigerous cysts.
Conclusion: According to the expression of — Bcl-2 in ameloblastoma and KCOT, and no
expression of EGFR in KCOT, it can be concluded that the biological activity and growth mechanisms
of KCOT are different compared with other cystic lesions. However, the aggressive potential of
KCOT is not as severe as that of a neoplasm such as ameloblastoma.
Key Words: Ameloblastoma, Bcl-2 protein, dentigerous cyst, epiderm, growth factor, epidermal growth factor receptor, immunohistochemistry, odontogenic tumor
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