Ahlaam Hosny Nassef, Hamed Mohamed Anwar Fouad, H. Raslan, A. M. Zahran, Ahmed Mohammad Hussein
{"title":"KIAA0101 IMMUNOHISTOCHEMICAL EXPRESSION IN DIAGNOSTIC DILEMMA BETWEEN AMELOBLASTOMA AND AMELOBLASTIC CARCINOMA (IN VITRO STUDY)","authors":"Ahlaam Hosny Nassef, Hamed Mohamed Anwar Fouad, H. Raslan, A. M. Zahran, Ahmed Mohammad Hussein","doi":"10.21608/adjalexu.2023.244645.1427","DOIUrl":null,"url":null,"abstract":"INTRODUCTION: Odontogenic tumors are a variety of oral lesions with clinical and histological variability. Some are benign, while others, like ameloblastoma, show infiltrative behavior. The most aggressive destructive odontogenic tumor is ameloblastic carcinoma. Diagnostic challenges arise in differentiating a malignant type from a classic benign ameloblastoma due to overlapping clinicopathologic features, prompting the use of immunohistochemical methods. KIAA0101, a nucleoprotein, is crucial for cell proliferation regulation, and its expression as a prognostic marker is being extensively researched in various human tumor sorts. However, its role in odontogenic tumors still needs more diagnostic research to be approved. Aim of the study: Evaluation of KIAA0101 immunoexpression in ameloblastoma and ameloblastic carcinoma. MATERIAL AND METHODS: Sixty blocks of human odontogenic tissues, divided equally into enamel organs (serving as a normal control), ameloblastoma, and ameloblastic carcinoma, were included in the study. Sections were stained with hematoxylin and eosin to determine an accurate histopathological diagnosis. Immunohistochemical analysis using the KIAA0101 antibody was performed using universal immunostaining techniques. RESULTS: Different immunoexpression of KIAA0101 were expressed in enamel organs, ameloblastoma, and ameloblastic carcinoma. The enamel organs showed the lowest expression levels, while the highest were detected in ameloblastic carcinoma. CONCLUSION : KIAA0101 produced a valuable indicator for tissue proliferation in ameloblastoma and ameloblastic carcinoma","PeriodicalId":7723,"journal":{"name":"Alexandria Dental Journal","volume":"122 21","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-07-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Alexandria Dental Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21608/adjalexu.2023.244645.1427","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
INTRODUCTION: Odontogenic tumors are a variety of oral lesions with clinical and histological variability. Some are benign, while others, like ameloblastoma, show infiltrative behavior. The most aggressive destructive odontogenic tumor is ameloblastic carcinoma. Diagnostic challenges arise in differentiating a malignant type from a classic benign ameloblastoma due to overlapping clinicopathologic features, prompting the use of immunohistochemical methods. KIAA0101, a nucleoprotein, is crucial for cell proliferation regulation, and its expression as a prognostic marker is being extensively researched in various human tumor sorts. However, its role in odontogenic tumors still needs more diagnostic research to be approved. Aim of the study: Evaluation of KIAA0101 immunoexpression in ameloblastoma and ameloblastic carcinoma. MATERIAL AND METHODS: Sixty blocks of human odontogenic tissues, divided equally into enamel organs (serving as a normal control), ameloblastoma, and ameloblastic carcinoma, were included in the study. Sections were stained with hematoxylin and eosin to determine an accurate histopathological diagnosis. Immunohistochemical analysis using the KIAA0101 antibody was performed using universal immunostaining techniques. RESULTS: Different immunoexpression of KIAA0101 were expressed in enamel organs, ameloblastoma, and ameloblastic carcinoma. The enamel organs showed the lowest expression levels, while the highest were detected in ameloblastic carcinoma. CONCLUSION : KIAA0101 produced a valuable indicator for tissue proliferation in ameloblastoma and ameloblastic carcinoma