Transcriptomic comparative study between canalicular adenoma and HMGA2::WIF1 canalicular-like pleomorphic adenoma

IF 5.4 2区 医学 Q1 ONCOLOGY
The Journal of Pathology Pub Date : 2026-07-07 Epub Date: 2026-04-29 DOI:10.1002/path.70070
Ziyad Alsugair, Anne Champagnac, Maxime Fieux, Pierre Philouze, Philippe Ceruse, Brice Thamphya, Daniel Pissaloux, Franck Tirode, Nazim Benzerdjeb
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引用次数: 0

Abstract

Canalicular adenoma (CA) is a benign salivary gland tumor predominantly affecting the upper lip and is characterized by monomorphic epithelial cells arranged in branching cords within a loose and vascularized stroma. Unlike pleomorphic adenoma (PA), CA lacks a chondroid matrix and exhibits specific histological features, such as high cuboidal to columnar cells arranged in one to two cell layers. A recently identified PA subtype, named ‘HMGA2-canalicular-like PA’, mimics the morphology of CA but affects major salivary glands, and harbors the HMGA2::WIF1 fusion. Immunohistochemical markers including SOX10 positivity and p40/p63 negativity are shared between these entities, raising questions about their molecular differences. Therefore, the current study aimed to extensively compare the molecular profiles of CAs and HMGA2-canalicular-like PAs to better understand the mechanisms underlying their oncogenesis. In the present study, CAs and the HMGA2-canalicular-like PAs mostly shared similar histology and immunostaining, while the clinical presentations regarding tumor site and transcriptomic profiles were different. A novel finding was the overexpression of SOX2 in patients diagnosed with CA, in comparison to those diagnosed with HMGA2-canalicular-like PA. The CAs displayed significantly higher enrichment of hallmarks for Hedgehog signaling, IL2/STAT5 signaling, and apical surface, and significantly lower enrichment of hallmarks for apoptosis and mitotic spindle. Additionally, Gene Ontology enrichment analysis displayed significant enrichment of biological process for CAs in comparison to HMGA2-canalicular-like PAs for myofibril assembly, muscle filament sliding, actin–myosin filament sliding, and sarcomere organization. CAs and HMGA2-canalicular-like PAs exhibited similar histology and immunostaining but differed significantly in tumor site and transcriptomic profiles. The latter revealed significant activation of muscle-related transcriptional pathways, and overexpression of SOX2 in CAs. © 2026 The Author(s). The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.

Abstract Image

管状腺瘤与HMGA2::WIF1管状多形性腺瘤的转录组学比较研究。
小管腺瘤(CA)是一种主要影响上唇的良性唾液腺肿瘤,其特征是在疏松的血管化基质内单形上皮细胞呈分支索状排列。与多形性腺瘤(PA)不同,CA缺乏软骨样基质,并表现出特定的组织学特征,如排列在一到两层细胞中的高立方体到柱状细胞。最近发现的一种PA亚型,名为“HMGA2-小管样PA”,模仿CA的形态,但影响主要唾液腺,并具有HMGA2::WIF1融合。包括SOX10阳性和p40/p63阴性在内的免疫组织化学标记在这些实体之间是共享的,这引发了关于它们的分子差异的问题。因此,本研究旨在广泛比较CAs和hmga2小管样PAs的分子谱,以更好地了解它们的肿瘤发生机制。在本研究中,ca与hmga2小管样PAs在组织学和免疫染色上大多相似,但在肿瘤部位和转录组谱方面的临床表现不同。一项新的发现是,与那些诊断为hmga2管样PA的患者相比,SOX2在CA患者中过表达。结果表明,这些CAs的Hedgehog信号、il - 2/STAT5信号和根尖表面的信号显著增加,而凋亡和有丝分裂纺锤体的信号显著减少。此外,Gene Ontology富集分析显示,与hmga2 -小管样PAs相比,CAs在肌原纤维组装、肌丝滑动、肌动蛋白-肌球蛋白丝滑动和肌节组织方面的生物过程显著富集。CAs和hmga2小管样PAs具有相似的组织学和免疫染色,但在肿瘤部位和转录组谱上存在显著差异。后者揭示了肌肉相关转录途径的显著激活,以及SOX2在CAs中的过表达。©2026作者。《病理学杂志》由John Wiley & Sons Ltd代表大不列颠和爱尔兰病理学会出版。
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
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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