PROLIFERATIVE ACTIVITY OF CALCIFYING ODONTOGENIC CYSTS AS EVALUATED BY PROLIFERATING CELL NUCLEAR ANTIGEN LABELING INDEX

Citation
T. Takata et al., PROLIFERATIVE ACTIVITY OF CALCIFYING ODONTOGENIC CYSTS AS EVALUATED BY PROLIFERATING CELL NUCLEAR ANTIGEN LABELING INDEX, Pathology international, 48(11), 1998, pp. 877-881
Citations number
26
Categorie Soggetti
Pathology
Journal title
ISSN journal
13205463
Volume
48
Issue
11
Year of publication
1998
Pages
877 - 881
Database
ISI
SICI code
1320-5463(1998)48:11<877:PAOCOC>2.0.ZU;2-R
Abstract
The calcifying odontogenic cyst (COC) presents with diverse histologic al features; thus, several subclassifications have been proposed. To e valuate the significance of the various histological features and subt ypes of COC from the perspective of proliferative activity, the prolif erating cell nuclear antigen (PCNA) labeling index (LI; the percentage of positive nuclei) was assessed immunohistochemically in 25 cases of COC (21 benign and four malignant). All of the benign cases were of t he cystic variety and further subclassified into non-proliferative sub type (NPS; four cases); proliferative subtype (PS; eight cases); and C OC associated with odontoma (COCaO, nine cases). The PCNA LI of the ma lignant COC (65.2 +/- 5.6) was significantly higher than that of the b enign COC (11.6 +/- 9.0; P = 0.002). Non-proliferative subtype (6.8 +/ - 2.8) showed the lowest PCNA LI and PS (17.2 +/- 11.2) the highest of among the three subtypes of benign cystic COC (P = 0.028). In nine ca ses of COCaO, six showed epithelial lining of the non-proliferative ty pe as NPS and the other three had lining with proliferative features a s PS. The PCNA LI of the latter COCaO group (14.3 +/- 6.6) was signifi cantly higher than that of the former (6.1 +/- 4.3; P = 0.05), as seen between PS and NPS. These results demonstrate that PCNA LI is a possi ble parameter for differentiating malignant COC from benign COC and, w hatever the subtypes, the proliferative features in the lining are the main factor influencing the proliferating activity of COC.