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Immunoexpression of Ki-67 MCM2 and MCM3 in Ameloblastoma and Ameloblastic Carcinoma and Their Correlations with Clinical and Histopathological Patterns

机译:Ki-67MCM2和MCM3在成釉细胞瘤和成膜细胞癌中的免疫表达及其与临床和组织病理学模式的关系

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摘要

Cell proliferation assays are performed using antibodies against nuclear proteins associated with DNA replication. These nuclear proteins have gained special interest to predict the biological and clinical behaviors of various tumors. The aim of this study was to analyze the presence of Ki-67 protein and the minichromosome maintenance-2 (MCM2) and maintenance-3 (MCM3) proteins in ameloblastoma. Materials and Methods. Cell proliferation marker expression levels were assessed via immunohistochemistry in 111 ameloblastoma cases (72 unicystic ameloblastoma samples, 38 solid/multicystic ameloblastoma samples, and 1 ameloblastic carcinoma). The label index was performed as described previously. Results. MCM2 and MCM3 showed higher proliferation indexes in all variants of ameloblastoma compared to the classic marker Ki-67. No correlation between the proliferation index and the clinical and protein expression data was observed. Conclusion. The results suggest that clinical features do not directly affect tumor cell proliferation. Moreover, the high levels of cellular proliferation of MCM2 and MCM3 compared with Ki-67 may indicate that MCM2 and MCM3 are more sensitive markers for predicting the growth rate and eventually might be helpful as a tool for predicting aggressive and recurrent behaviors in these tumors.
机译:使用针对与DNA复制相关的核蛋白的抗体进行细胞增殖测定。这些核蛋白已引起人们对预测各种肿瘤的生物学和临床行为的特殊兴趣。这项研究的目的是分析成釉细胞瘤中Ki-67蛋白和微染色体维持2(MCM2)和维持3(MCM3)蛋白的存在。材料和方法。通过免疫组织化学在111例成釉细胞瘤病例(72个单囊性成釉细胞瘤样品,38个实体/多囊性成釉细胞瘤样品和1个成釉细胞癌)中评估细胞增殖标志物的表达水平。如前所述执行标签索引。结果。与经典标记物Ki-67相比,MCM2和MCM3在成釉细胞瘤的所有变体中均显示出更高的增殖指数。没有观察到增殖指数与临床和蛋白质表达数据之间的相关性。结论。结果表明临床特征并不直接影响肿瘤细胞的增殖。此外,与Ki-67相比,MCM2和MCM3的细胞增殖水平高可能表明MCM2和MCM3是预测生长速率的更敏感标记,最终可能有助于预测这些肿瘤的侵袭性和复发行为。

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