Comparison of the value of PCNA and Ki-67 as markers of cell proliferation in ameloblastic tumors

被引:187
|
作者
Bologna-Molina, Ronell [1 ,2 ]
Mosqueda-Taylor, Adalberto [3 ]
Molina-Frechero, Nelly [3 ]
Mori-Estevez, Ana-Dolores [4 ]
Sanchez-Acuna, Guillermo [5 ]
机构
[1] UJED, Res Dept, Sch Dent, Durango, Mexico
[2] Univ Republ UDELAR, Sch Dent, Montevideo, Uruguay
[3] Univ Autonoma Metropolitana, Hlth Care Dept, Mexico City, DF, Mexico
[4] Hosp Univ Gral Calixto Garcia La Havana, Dept Pathol, Havana, Cuba
[5] Hosp Univ Gral Calixto Garcia La Havana, Maxillofacial Dept, Havana, Cuba
来源
MEDICINA ORAL PATOLOGIA ORAL Y CIRUGIA BUCAL | 2013年 / 18卷 / 02期
关键词
Ameloblastomas; ameloblastic carcinoma; PCNA; Ki-67; cell proliferation markers; LYMPH-NODE METASTASIS; NUCLEAR ANTIGEN; CARCINOMA; EXPRESSION; PROTEINS; SURVIVAL; CANCER; BCL-2; HEAD; KI67;
D O I
10.4317/medoral.18573
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objectives: The aim of this study was to compare among PCNAand Ki-67 as the most reliable immunohistochemical marker for evaluating cell proliferation in ameloblastic tumors. Study Design: Observational, retrospective, and descriptive study of a large series of ameloblastic tumors, composed of 161 ameloblastomas and four ameloblastic carcinomas, to determine and compare PCNA and Ki-67 expression using immunohistochemistry techniques. Results: When analyzing Ki-67 positivity, the desmoplastic ameloblastoma demonstrated a significantly lower proliferation rate (1.9%) compared with the solid/multicystic and unicystic ameloblastomas and ameloblastic carcinomas (p<0.05), whereas the ameloblastic carcinomas displayed a significantly higher rate compared with all of the other ameloblastomas (48.7%) (p<0.05). When analyzing cell proliferation with PCNA, we found significant differences only between the ameloblastic carcinomas (93.3%) and the desmoplastic ameloblastomas (p<0.05). When differences between the immunopositivity for PCNA and Ki-67 were compared, the percentages were higher for PCNA in all types of ameloblastomas and ameloblastic carcinomas. In all cases, the percentages were greater than 80%, whereas the immunopositivity for Ki-67 was significantly lower; for example, the ameloblastic carcinoma expressed the highest positivity and only reached 48.7%, compared to 93.3% when we used PCNA. Conclusions: In the present study, when we used the proliferation cell marker Ki-67, the percentages of positivity were more specific and varied among the different types of ameloblastomas, suggesting that Ki-67 is a more specific marker for the proliferation of ameloblastic tumor cells.
引用
收藏
页码:E174 / E179
页数:6
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