The Correlation of p53, CK13, CK17, and Ki67 Immunostaining Patterns in Assisting the Histopathologic Grading of Oral Epithelial Dysplasia

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Dr. Julia Yu-Fong Chang , Dr. Yi-Ping Wang
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Abstract

Introduction

Different markers, such as p53, CK13, CK17, and Ki67, have been used to assist in the histopathologic grading of oral epithelial dysplasia (OED). This study aims to evaluate the correlation between these markers and histopathologic grading.

Materials and Methods

This retrospective study included 65 OED cases: 15 with mild dysplasia, 31 with moderate dysplasia, and 19 with severe dysplasia. Patient age, gender, lesion location, histopathologic grading, and expression patterns of p53, CK13, CK17, and Ki67 immunohistochemical studies were reviewed and analyzed.

Results

In our cases, half of the mild dysplasia and all of the moderate and severe dysplasia cases showed a reverse CK13/CK17 staining pattern. An increased number of Ki67-positive cells, located upward, were frequently associated with moderate and severe dysplasia cases. However, mutated p53 staining patterns were correlated with severe dysplasia (16/19; 84.2%). All our mild dysplasia cases showed a wild-type p53 staining pattern, and fewer than one-third (7/31; 22.6%) of moderate dysplasia cases revealed a mutated p53 staining pattern. The staining patterns were not associated with patient age and gender. Lesions at the ventral and lateral border of the tongue and soft palate were mainly associated with a mutated p53 staining pattern (12/14; 85.7% and 3/3; 100%, respectively). Only 17.5% (7/40) of the lesions on the buccal mucosa were associated with mutated p53.

Conclusions

The alteration in the CK13/17 staining pattern can be used to detect differentiation changes in early OED. Mutation of p53 is most likely a later event and is associated with more advanced OED.

p53、CK13、CK17 和 Ki67 免疫染色模式在辅助口腔上皮增生症组织病理学分级中的相关性
导言p53、CK13、CK17和Ki67等不同标记物已被用于辅助口腔上皮发育不良(OED)的组织病理学分级。本研究旨在评估这些标记物与组织病理学分级之间的相关性:15 例轻度发育不良,31 例中度发育不良,19 例重度发育不良。回顾并分析了患者的年龄、性别、病变位置、组织病理学分级以及p53、CK13、CK17和Ki67免疫组化研究的表达模式。中度和重度发育不良病例常伴有Ki67阳性细胞数量增加,且位于上部。然而,突变的 p53 染色模式与重度发育不良相关(16/19;84.2%)。我们的所有轻度发育不良病例都显示出野生型 p53 染色模式,只有不到三分之一(7/31;22.6%)的中度发育不良病例显示出突变的 p53 染色模式。染色模式与患者的年龄和性别无关。舌和软腭腹侧和外侧边缘的病变主要与突变的p53染色模式有关(分别为12/14;85.7%和3/3;100%)。结论 CK13/17染色模式的改变可用于检测早期OED的分化变化。CK13/17染色模式的改变可用于检测早期OED的分化变化,而p53突变很可能发生在晚期,并与更晚期的OED相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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