探索以 TRPS1::PLAG1 基因融合为特征的皮肤混合瘤的分子图谱。

IF 5.6 2区 医学 Q1 ONCOLOGY The Journal of Pathology Pub Date : 2024-10-29 DOI:10.1002/path.6359
Ziyad Alsugair, Marie Donzel, Nicolas Macagno, Juliet Tantot, Olivier Harou, Maxime Battistella, Pierre Sohier, Thibault Kervarrec, Arnaud de la Fouchardière, Brigitte Balme, Anne Champagnac, Marie-Delphine Lanic, Jonathan Lopez, Marick Laé, Françoise Descotes, Franck Tirode, Daniel Pissaloux, Brice Thamphya, Valérie Costes-Martineau, Nazim Benzerdjeb
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引用次数: 0

摘要

在某些面部区域发现的多形性腺瘤(PA)和皮肤混合瘤(CMT)在组织学上具有相似性,这给诊断带来了挑战。分子研究结果显示,PA 和 CMT 具有共同的遗传特征,尤其是 PLAG1 基因重排。虽然分子上的区别受到的关注有限,但我们的观察结果表明,有多例 CMT 携带 TRPS1::PLAG1 融合基因。这一临床经验促使我们研究 TRPS1::PLAG1 融合对确定肿瘤来源的潜在诊断作用。我们从法国医疗机构获得了两组数据,包括 46 例 CMT 和 45 例唾液腺 PA,并由各亚专科的专家进行了审查。通过 RNA 测序分析,确定了携带 PLAG1 的病例的分子特征。收集了临床、病理和分子数据。在这项研究中,CMT病例表现出复发性基因融合,主要是TRPS1::PLAG1(74%)。这些肿瘤具有共同的组织学特征,包括55%的病例为输卵管分化,不同比例的病例为鳞状化生。与此相反,PA 病例的基因融合涉及 PLAG1 与各种基因伙伴的融合,只有一例确定了 TRPS1::PLAG1。在转录组水平上也观察到 TRPS1::PLAG1 CMT 与其他肿瘤之间存在这种差异。然而,TRPS1 免疫染色与 TRPS1::PLAG1 融合并不相关。总之,我们报告称,复发性 TRPS1::PLAG1 融合型 CMT 表现出相似的组织学特征,包括约半数病例伴有鳞状化生的输卵管分化。这种融合的检测对于正确识别这些肿瘤的来源很有价值。© 2024 大不列颠及爱尔兰病理学会。
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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Exploring the molecular landscape of cutaneous mixed tumors characterized by TRPS1::PLAG1 gene fusion

The histological similarities between pleomorphic adenomas (PAs) and cutaneous mixed tumors (CMTs) found in certain facial regions can create a diagnostic challenge. Molecular findings reveal common genetic profiles, particularly PLAG1 rearrangements in both PA and CMT. Although molecular distinctions have received limited attention, our observations indicate multiple cases of CMTs carrying the TRPS1::PLAG1 fusion. This clinical experience has driven our investigation into the potential diagnostic utility of TRPS1::PLAG1 fusions for determining tumor origin. Two cohorts consisting of 46 cases of CMT and 45 cases of PA of the salivary glands were obtained from French institutions and reviewed by specialists in each subspecialty. RNA sequencing analysis was conducted to identify the molecular features of cases harboring PLAG1. Clinical, pathological, and molecular data were collected. In this study, cases of CMT exhibited recurrent gene fusions, primarily TRPS1::PLAG1 (74%). These tumors shared characteristic histological features, including tubuloductal differentiation in 55% of cases and squamous metaplasia in varying proportions. In contrast, cases of PA had gene fusions involving PLAG1 with various gene partners, with only one case in which TRPS1::PLAG1 was identified. This disparity was also observed at the transcriptomic level between TRPS1::PLAG1 CMTs and other tumors. However, TRPS1 immunostaining did not correlate with TRPS1::PLAG1 fusion. In conclusion, we report that recurrent TRPS1::PLAG1 fusion CMTs exhibit similar characteristic histological features, including tubuloductal differentiation that is associated with squamous metaplasia in around half of cases. Detection of this fusion could be valuable in correctly identifying the origin of these tumors. © 2024 The Pathological Society of Great Britain and Ireland.

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来源期刊
The Journal of Pathology
The Journal of Pathology 医学-病理学
CiteScore
14.10
自引率
1.40%
发文量
144
审稿时长
3-8 weeks
期刊介绍: The Journal of Pathology aims to serve as a translational bridge between basic biomedical science and clinical medicine with particular emphasis on, but not restricted to, tissue based studies. The main interests of the Journal lie in publishing studies that further our understanding the pathophysiological and pathogenetic mechanisms of human disease. The Journal of Pathology welcomes investigative studies on human tissues, in vitro and in vivo experimental studies, and investigations based on animal models with a clear relevance to human disease, including transgenic systems. As well as original research papers, the Journal seeks to provide rapid publication in a variety of other formats, including editorials, review articles, commentaries and perspectives and other features, both contributed and solicited.
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