Sympathetic axonogenesis promotes adenoid cystic carcinoma progression.

IF 12.6 1区 医学 Q1 IMMUNOLOGY
Journal of Experimental Medicine Pub Date : 2025-07-07 Epub Date: 2025-04-24 DOI:10.1084/jem.20242250
Chun-Hao Chen, Boris Reva, Nora Katabi, Avishai Wizel, Hongbo Xu, Alan L Ho, Luc G T Morris, Richard L Bakst, Anuraag S Parikh, Yotam Drier, Sylvie Deborde, Richard J Wong
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引用次数: 0

Abstract

Nerves are integral to the adenoid cystic carcinoma (ACC) microenvironment. The strong association of ACC with perineural invasion (PNI) is considered a hallmark of this disease. In human salivary ACC, we identify intratumoral, small-caliber, disorganized sympathetic nerves not observed in other salivary neoplasms. Norepinephrine or sympathetic ganglia explants enhance ACC proliferation in vitro. Two novel orthotopic ACC patient-derived xenograft (PDX) models recapitulate ACC morphology and demonstrate sympathetic innervation. Pharmacologic or surgical blockade of sympathetic nerves decreases ACC PDX growth. Bulk RNA sequencing of salivary ACC reveals correlations between noradrenergic nerve development signatures and worse patient survival. Metastatic ACC foci exhibit lower nerve signature gene expression levels than primary ACC. Sympathetic innervation in ACC is distinct from PNI and reflects tumor axonogenesis driven by noradrenergic neural development programs. These programs support ACC progression, are associated with poor prognosis, and may be inhibited as a therapeutic strategy.

交感轴突发生促进腺样囊性癌进展。
神经是腺样囊性癌(ACC)微环境的组成部分。ACC与神经周围侵袭(PNI)的强烈关联被认为是该疾病的标志。在人类唾液ACC中,我们发现了肿瘤内,小口径,无序的交感神经,而在其他唾液肿瘤中没有观察到。去甲肾上腺素或交感神经节外植体可促进ACC体外增殖。两种新的原位ACC患者来源的异种移植(PDX)模型概括了ACC的形态并显示了交感神经支配。药物或手术阻断交感神经可减少ACC PDX的生长。唾液ACC的大量RNA测序揭示了去甲肾上腺素能神经发育特征与患者生存差之间的相关性。转移性ACC病灶表现出较原发性ACC低的神经特征基因表达水平。ACC的交感神经支配与PNI不同,反映了由去肾上腺素能神经发育程序驱动的肿瘤轴突发生。这些方案支持ACC进展,与不良预后相关,可作为一种治疗策略加以抑制。
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来源期刊
CiteScore
26.60
自引率
1.30%
发文量
189
审稿时长
3-8 weeks
期刊介绍: Since its establishment in 1896, the Journal of Experimental Medicine (JEM) has steadfastly pursued the publication of enduring and exceptional studies in medical biology. In an era where numerous publishing groups are introducing specialized journals, we recognize the importance of offering a distinguished platform for studies that seamlessly integrate various disciplines within the pathogenesis field. Our unique editorial system, driven by a commitment to exceptional author service, involves two collaborative groups of editors: professional editors with robust scientific backgrounds and full-time practicing scientists. Each paper undergoes evaluation by at least one editor from both groups before external review. Weekly editorial meetings facilitate comprehensive discussions on papers, incorporating external referee comments, and ensure swift decisions without unnecessary demands for extensive revisions. Encompassing human studies and diverse in vivo experimental models of human disease, our focus within medical biology spans genetics, inflammation, immunity, infectious disease, cancer, vascular biology, metabolic disorders, neuroscience, and stem cell biology. We eagerly welcome reports ranging from atomic-level analyses to clinical interventions that unveil new mechanistic insights.
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