唾液酸细胞癌中的 PON3::LCN1 和 HTN3::MSANTD3 基因融合与 NR4A3/NR4A2 表达

Lijing Zhu, Lisha Sun, Ye Zhang, Xiaoxiao Liu, XueFen Li, Zheng Zhou, Yajuan Cui, Chuan-Xiang Zhou, Tie-Jun Li
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引用次数: 0

摘要

唾液腺醋酸细胞癌(AciCC)是一种低级别癌症,其特征是转录因子核受体亚家族 4 A 组 3(NR4A3)的过度表达。AciCC 一直是一些分子研究项目的主题。本研究深入研究了AciCC的分子图谱,以确定更多的改变并探讨其临床意义。本研究对 41 例 AciCC 和 11 例分泌性癌 (SC) 样本进行了 RNA 测序和标记物 NR4A3/NR4A2、DOG-1、S100 和乳球蛋白的免疫组化染色。在 35 个 AciCC 中发现了 NR4A3,其余 6 个样本为 NR4A3 阴性和 NR4A2 阳性;SC 样本始终为 NR4A3 阴性。在9/41(21.9%)例AciCC中检测到了一种新型融合,即PON3外显子1-LCN1外显子5,表现出一种典型的组织学模式,即浆液细胞成分与夹层导管样成分一起呈固态片状生长。对 39 名患者进行了中位 59 个月的临床随访,结果显示了不同的预后结果:34例患者无疾病迹象,而其余5例患者预后较差,包括局部复发、淋巴结和远处转移以及疾病相关死亡,其中4例患者携带PON3::LCN1融合基因。此外,在 7/41 例 AciCC 患者中反复发现了 HTN3::MSANTD3 融合。SC患者缺乏这两种融合。免疫组化发现不同样本中DOG-1、S100和mammaglobin的表达存在差异,这为了解它们在AciCC中的作用提供了细微的线索。这项研究强调了PON3::LCN1和HTN3::MSANTD3融合是AciCC中反复出现的分子事件,具有潜在的诊断和预后作用,并推动了对靶向治疗策略的进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PON3::LCN1 and HTN3::MSANTD3 Gene Fusions With NR4A3/NR4A2 Expression in Salivary Acinic Cell Carcinoma.
Acinic cell carcinoma of the salivary gland (AciCC) is a low-grade carcinoma characterized by the overexpression of the transcription factor nuclear receptor subfamily 4 group A member 3 (NR4A3). AciCC has been the subject of a few molecular research projects. This study delves into AciCC's molecular landscape to identify additional alterations and explore their clinical implications. RNA sequencing and immunohistochemical staining for markers NR4A3/NR4A2, DOG-1, S100, and mammaglobin were utilized on 41 AciCCs and 11 secretory carcinoma (SC) samples. NR4A3 was evident in 35 AciCCs, while the residual 6 were NR4A3-negative and NR4A2-positive; SC samples were consistently NR4A3-negative. A novel fusion, PON3 exon 1-LCN1 exon 5, was detected in 9/41 (21.9%) AciCCs, exhibiting a classical histologic pattern with serous cell components growing in solid sheets alongside the intercalated duct-like component. Clinical follow-up of 39 patients over a median of 59 months revealed diverse prognostic outcomes: 34 patients exhibited no disease evidence, whereas the remaining 5 experienced poorer prognosis, involving local recurrence, lymph node, and distant metastasis, and disease-associated death, 4 of which harbored the PON3::LCN1 fusion. In addition, the HTN3::MSANTD3 fusion was recurrently identified in 7/41 AciCC cases. SC patients lacked both fusions. Immunohistochemistry uncovered differential expression of DOG-1, S100, and mammaglobin across samples, providing nuanced insights into their roles in AciCC. This study accentuates PON3::LCN1 and HTN3::MSANTD3 fusions as recurrent molecular events in AciCC, offering potential diagnostic and prognostic utility and propelling further research into targeted therapeutic strategies.
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