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PON3::LCN1and HTN3::MSANTD3Gene Fusions With NR4A3/NR4A2 Expression in Salivary Acinic Cell Carcinoma

Authors :
Zhu, Lijing
Sun, Lisha
Zhang, Ye
Liu, Xiaoxiao
Li, XueFen
Zhou, Zheng
Cui, Yajuan
Zhou, Chuan-Xiang
Li, Tie-jun
Source :
The American Journal of Surgical Pathology; June 2024, Vol. 48 Issue: 6 p681-690, 10p
Publication Year :
2024

Abstract

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, PON3exon 1–LCN1exon 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::LCN1fusion. In addition, the HTN3::MSANTD3fusion 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::LCN1and HTN3::MSANTD3fusions as recurrent molecular events in AciCC, offering potential diagnostic and prognostic utility and propelling further research into targeted therapeutic strategies.

Details

Language :
English
ISSN :
01475185 and 15320979
Volume :
48
Issue :
6
Database :
Supplemental Index
Journal :
The American Journal of Surgical Pathology
Publication Type :
Periodical
Accession number :
ejs66400628
Full Text :
https://doi.org/10.1097/PAS.0000000000002219