SOX10 Expression in Primary Salivary Gland Tumors: A Meta-Analysis.

IF 4.1
Otto Tahvanainen, Henri Lagerstam, David Kalfert, Ivana Kholová
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Abstract

Purpose: Primary salivary gland tumors form a heterogeneous group with diagnostic challenges. Sex-determining region Y-related homeobox 10 (SOX10) is a transcription factor studied in primary salivary gland tumors for over a decade. To date, no systematic review or meta-analysis has been conducted on its expression in salivary gland tumors.

Methods: A PubMed literature search identified all studies in which SOX10 was evaluated by immunohistochemistry in primary salivary gland tumors. Information on SOX10 positivity, staining pattern, percentage of positive cells, and information on the antibody source and clone were tabulated in Microsoft Excel. The meta-analysis was performed with OpenMeta Analyst. The meta-analysis adheres to PRISMA (Preferred Reporting Items for Systematic reviews and Meta-Analyses) guidelines.

Results: The meta-analysis included 35 studies with 1146 histological and 35 cytological samples immunostained with SOX10. The list of SOX10-positive tumors according to our meta-analysis includes pleomorphic adenoma (pooled meta-analytic estimate of SOX10 positivity 95.8%, 95% CI 91.7-99.9%), polymorphous adenocarcinoma (pooled estimate 97.4%, 95% CI 92.3-102.6%), canalicular adenoma (pooled estimate 98.9%, 95% CI 96.4-101.4%), basal cell adenoma (pooled estimate 91.3%, 95% CI 80.2-102.5%), adenoid cystic carcinoma (pooled estimate 96.6%, 95% CI 94.1-99.2%), myoepithelioma (pooled estimate 75.2%, 95% CI 52.0-98.4%), acinic cell carcinoma (pooled estimate 97.4%, 95% CI 94.1-100.6%), intercalated duct type of intraductal carcinoma (pooled estimate 90.8%, 95% CI 75.9-105.8%), and microsecretory carcinoma (pooled estimate 96.1%, 95% CI 87.2-105.0%). Limited evidence suggests that basal cell adenocarcinoma, epithelial-myoepithelial carcinoma, and myoepithelial carcinoma are also SOX10 positive. SOX10-negative entities include Warthin's tumor (pooled estimate 2.3%, 95% CI 0-7.0%), apocrine type of intraductal carcinoma (pooled estimate 10.3%, 95% CI - 10.4-31.1%), salivary duct carcinoma (pooled estimate 3.7%, 95% CI - 0.6-8.1%), and oncocytoma (pooled estimate 8.0%, 95% CI - 2.7-18.7%). Polyclonal antibodies and clones EP268, N-20, and A-2 provided similar results. Clone BC34 stained a lower percentage of SOX10-positive tumors.

Conclusion: This meta-analysis lists SOX10-positive and -negative tumors. This demonstrates the necessity of subtype-specific reporting and stating the antibody clone used in immunohistochemical studies.

原发性唾液腺肿瘤中SOX10的表达:一项meta分析
目的:原发性唾液腺肿瘤是一种异质性的肿瘤,具有诊断挑战性。性别决定区y相关同源盒10 (SOX10)是一个在原发性唾液腺肿瘤中研究了十多年的转录因子。迄今为止,尚未对其在唾液腺肿瘤中的表达进行系统评价或荟萃分析。方法:PubMed文献检索确定了所有用免疫组织化学方法评价原发性唾液腺肿瘤中SOX10的研究。将SOX10阳性信息、染色模式、阳性细胞百分比、抗体来源和克隆信息在Microsoft Excel中制表。meta分析使用OpenMeta Analyst进行。荟萃分析遵循PRISMA(系统评价和荟萃分析首选报告项目)指南。结果:荟萃分析纳入35项研究,1146例组织学和35例细胞学样本进行SOX10免疫染色。根据我们的荟萃分析,SOX10阳性肿瘤包括多形性腺瘤(综合荟萃分析估计SOX10阳性95.8%,95% CI 91.7-99.9%)、多形态腺癌(综合估计97.4%,95% CI 92.3-102.6%)、管状腺瘤(综合估计98.9%,95% CI 96.4-101.4%)、基底细胞腺瘤(综合估计91.3%,95% CI 80.2-102.5%)、腺样囊性癌(综合估计96.6%,95% CI 94.1-99.2%)、肌上皮瘤(综合估计75.2%,(95% CI 52.0-98.4%),腺泡细胞癌(合并估计97.4%,95% CI 94.1-100.6%),导管间插型导管内癌(合并估计90.8%,95% CI 75.9-105.8%)和微分泌性癌(合并估计96.1%,95% CI 87.2-105.0%)。有限的证据表明基底细胞腺癌、上皮-肌上皮癌和肌上皮癌也是SOX10阳性。sox10阴性实体包括Warthin肿瘤(综合估计为2.3%,95% CI为0-7.0%)、大汗液型导管内癌(综合估计为10.3%,95% CI为10.4-31.1%)、唾液管癌(综合估计为3.7%,95% CI为0.6-8.1%)和嗜瘤细胞瘤(综合估计为8.0%,95% CI为2.7-18.7%)。多克隆抗体和克隆EP268、N-20和A-2提供了类似的结果。克隆BC34染色sox10阳性肿瘤的百分比较低。结论:本荟萃分析列出了sox10阳性和阴性的肿瘤。这证明了在免疫组织化学研究中进行亚型特异性报告和说明抗体克隆的必要性。
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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