Syndecan-1(CD138)和podoplanin在牙源性角化囊性肿瘤、角化牙源性囊肿和含牙囊肿中表达的免疫组化比较研究

Alka Chahar, P. Narain, Naveen Chahar, J. Gupta, Arpita Kabiraj
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引用次数: 0

摘要

背景:由于病理学家之间组织学的重叠,牙源性病变可能会给诊断带来挑战。因此,提供准确诊断的肿瘤标志物很少。Syndecan-1(CD-138)和podoplanin(PDPN)是蛋白聚糖,已被描述为各种牙源性病变的重要诊断和预后标志物。目的:本研究旨在评估和比较syndecan-1(CD-138)和podoplanin在角化囊性牙源性肿瘤、正角化牙源性囊肿(OOC)和齿状囊肿(DC)中的免疫组织化学表达。材料和方法:从科室档案中提取KCOT、OOC和DC的福尔马林固定石蜡包埋组织块。使用旋转切片机制作三个切片,每个切片厚度为3μm,并使用免疫组织化学方法和标准苏木精和伊红染色,用辛迪加-1(CD-138)和足平蛋白(PDPN)对其进行染色。结果:syndecan-1在KCOT中的免疫组织化学表达在6例中呈弱至中度阳性,其中2例呈阳性。在OOC中,3例表现为阴性表达-1,而7例表现为弱至中度阳性。足平蛋白在KCOT中的免疫组织化学表达在4例中观察到弱至中度阳性,其中5例表现出强阳性表达。在OOC中,3例podoplanin免疫组织化学表达阴性,4例强阳性。DC中的足平蛋白免疫反应性有3例为阴性,而5例为弱至中度阳性。结论:syndecan-1和podoplanin的表达之间缺乏显著相关性,这加强了这些蛋白在牙源性病变分化中的确切作用,需要进一步阐明。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A comparative immunohistochemical study of expression of Syndecan-1 (CD138) and podoplanin in keratocystic odontogenic tumor, orthokeratinized odontogenic cyst and dentigerous cyst
Background: Odontogenic lesions can bring about diagnostic challenges due to overlapping histology among pathologists. Thus, there are few tumor markers that provide accurate diagnosis. Syndecan-1 (CD-138) and podoplanin (PDPN) are proteoglycans that have been described as substantial diagnostic and prognostic markers in various odontogenic lesions. Aim: This study aims to evaluate and compare the immunohistochemical expression of syndecan-1 (CD-138) and podoplanin in keratocystic odontogenic tumor, orthokeratinized odontogenic cyst (OOC), and dentigerous cyst (DC). Materials and Methods: The formalin-fixed paraffin-embedded tissue blocks of KCOT, OOC, and DCs were retrieved form the archives of department. Three sections each of 3 μm thickness were made using a rotary microtome and they were stained with syndecan-1 (CD-138) and podoplanin (PDPN) using immunohistochemical methods and standard hematoxylin and eosin stain. Results: Immunohistochemical expression of syndecan-1in KCOT was found to be weakly to moderately positive in 6 cases with 2 cases exhibiting positive expression. In OOC, 3 cases displayed negative expression-1 whereas 7 cases were weakly to moderately positive. Immunohistochemical expression of podoplanin in KCOT was observed to be weakly to moderately positive in 4 cases with 5 cases exhibiting strongly positive expression. In OOC, 3 cases displayed negative immunohistochemical expression for podoplanin and 4 cases were strongly positive. Immunoreactivity for podoplanin in DC was negative in 3 cases whereas 5 cases were weakly to moderately positive. Conclusion: The absence of significant correlation between expression of syndecan-1 and podoplanin reinforces the exact role of these proteins in the differentiation of odontogenic lesions which need to be elucidated further.
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