PON3::LCN1 and HTN3::MSANTD3 Gene Fusions With NR4A3/NR4A2 Expression in Salivary Acinic Cell Carcinoma

被引:0
|
作者
Zhu, Lijing [1 ,2 ,3 ,4 ,5 ]
Sun, Lisha [2 ,3 ,4 ,5 ,6 ]
Zhang, Ye [1 ,2 ,3 ,4 ,5 ]
Liu, Xiaoxiao [7 ]
Li, XueFen [6 ]
Zhou, Zheng [1 ,2 ,3 ,4 ,5 ]
Cui, Yajuan [1 ,2 ,3 ,4 ,5 ]
Zhou, Chuan-Xiang [1 ,2 ,3 ,4 ,5 ]
Li, Tie-jun [1 ,2 ,3 ,4 ,5 ]
机构
[1] Peking Univ, Sch & Hosp Stomatol, Dept Oral Pathol, Beijing 100081, Peoples R China
[2] Natl Ctr Stomatol, Beijing, Peoples R China
[3] Natl Clin Res Ctr Oral Dis, Beijing, Peoples R China
[4] Natl Engn Res Ctr Oral Biomat & Digital Med Device, Beijing, Peoples R China
[5] Chinese Acad Med Sci 2019RU034, Res Unit Precis Pathol Diag Tumors Oral & Maxillof, Beijing, Peoples R China
[6] Peking Univ, Sch & Hosp Stomatol, Cent Lab, Beijing, Peoples R China
[7] Shanghai Jiao Tong Univ, Sch Med, Shanghai Peoples Hosp 9, Dept Periodontol, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
acinic cell carcinoma; PON3::LCN1 fusion; HTN3::MSANTD3 fusion; gene fusion; salivary gland neoplasms; GLAND; HEAD; SCAVENGER;
D O I
10.1097/PAS.0000000000002219
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
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.
引用
收藏
页码:681 / 690
页数:10
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