Slusarenko da Silva Yuri, Naclério-Homem Maria da Graça
School of Dentistry, UniFG University Center (Faculty of Guanambi), Avenida Pedro Felipe Duarte 4911 São Sebastião, Guanambi, Bahia, 46430-000, Brazil.
Department of Oral & Maxillofacial Surgery, Traumatology and Prosthesis - Faculty of Dentistry, University of São Paulo, São Paulo, Brazil.
Oral Maxillofac Surg. 2020 Sep;24(3):277-282. doi: 10.1007/s10006-020-00856-5. Epub 2020 Jun 3.
The purpose of this study is to find out if the biological behavior and the capacity of the odontogenic keratocyst (OKC) in maintaining pathologic cells alive are more similar to the dentigerous cyst or to the ameloblastoma by assessing bcl-2. We searched MEDLINE, Web of Science, and Scopus for immunohistochemical studies reporting OKCs, dentigerous cysts, and ameloblastomas. Risk difference between the lesions expressing bcl-2 was the effect measure and a P value < 0.05 was considered to provide evidence to the effect estimates. OKCs have an estimated difference of 91% in the probability to express the bcl-2 over dentigerous cysts, but there is no difference in the expression of bcl-2 between OKCs and ameloblastomas. The present study demonstrated a great risk difference in the expression of bcl-2 between OKCs and dentigerous cysts and no risk difference between OKCs and ameloblastomas. OKC's growth may indirectly be attributed to the anti-apoptotic effect of bcl-2 in the cystic epithelium and not only to the increase of its intraluminal pressure. Therefore, the classification of this lesion into keratocystic odontogenic tumor should be carefully reconsidered.
本研究的目的是通过评估bcl-2,来确定牙源性角化囊肿(OKC)的生物学行为以及维持病理细胞存活的能力,与含牙囊肿或成釉细胞瘤相比,哪一个更为相似。我们在MEDLINE、科学网和Scopus数据库中检索了报告OKC、含牙囊肿和成釉细胞瘤的免疫组织化学研究。表达bcl-2的病变之间的风险差异为效应量,P值<0.05被认为可为效应估计提供证据。与含牙囊肿相比,OKC表达bcl-2的概率估计差异为91%,但OKC与成釉细胞瘤之间bcl-2的表达没有差异。本研究表明,OKC与含牙囊肿之间bcl-2的表达存在很大的风险差异,而OKC与成釉细胞瘤之间不存在风险差异。OKC的生长可能间接归因于bcl-2在囊性上皮中的抗凋亡作用,而不仅仅是其管腔内压力的增加。因此,应仔细重新考虑将该病变归类为角化囊性牙源性肿瘤。