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Ki-67、MCM2和MCM3在成釉细胞瘤和成釉细胞癌中的免疫表达及其与临床和组织病理学模式的相关性

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

作者信息

Carreón-Burciaga Ramón Gil, González-González Rogelio, Molina-Frechero Nelly, Bologna-Molina Ronell

机构信息

Research Department, School of Dentistry, Universidad Juárez del Estado de Durango (UJED), 34000 Durango, DGO, Mexico.

Health Care Department, Universidad Autónoma Metropolitana, Xochimilco, 04960 Mexico City, DF, Mexico.

出版信息

Dis Markers. 2015;2015:683087. doi: 10.1155/2015/683087. Epub 2015 Dec 28.

DOI:10.1155/2015/683087
PMID:26823641
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4707386/
Abstract

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.

摘要

细胞增殖分析使用针对与DNA复制相关的核蛋白的抗体来进行。这些核蛋白在预测各种肿瘤的生物学和临床行为方面引起了特别关注。本研究的目的是分析成釉细胞瘤中Ki-67蛋白、微小染色体维持蛋白2(MCM2)和维持蛋白3(MCM3)的存在情况。材料与方法。通过免疫组织化学评估111例成釉细胞瘤病例(72例单囊性成釉细胞瘤样本、38例实性/多囊性成釉细胞瘤样本和1例成釉细胞癌)中细胞增殖标志物的表达水平。标记指数如前所述进行测定。结果。与经典标志物Ki-67相比,MCM2和MCM3在成釉细胞瘤的所有变体中显示出更高的增殖指数。未观察到增殖指数与临床及蛋白表达数据之间的相关性。结论。结果表明临床特征不会直接影响肿瘤细胞增殖。此外,与Ki-67相比,MCM2和MCM3的高细胞增殖水平可能表明MCM2和MCM3是预测生长速度更敏感的标志物,最终可能有助于作为预测这些肿瘤侵袭性和复发性行为的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b177/4707386/3c2ae45d7705/DM2015-683087.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b177/4707386/e137d01ee764/DM2015-683087.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b177/4707386/79eddf3adf02/DM2015-683087.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b177/4707386/3c2ae45d7705/DM2015-683087.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b177/4707386/e137d01ee764/DM2015-683087.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b177/4707386/79eddf3adf02/DM2015-683087.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b177/4707386/3c2ae45d7705/DM2015-683087.003.jpg

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