Feng Guanying, Guo Yibo, Chen Mingtao, Zhang Yu, Liu Zheqi, Sun Chen, Hu Xin, Lin Chengzhong, Liu Yu, Wu Yue, Wu Hao, Yang Xi, Wang Yang, Ye Jinhai, Liu Jiannan, Wang Xu, Ji Tong, Zhang Chenping
Department of Oral Maxillofacial-Head Neck Oncology, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
College of Stomatology, Shanghai Jiao Tong University, Shanghai, China.
Oral Dis. 2025 Apr;31(4):1140-1153. doi: 10.1111/odi.15214. Epub 2024 Dec 5.
To investigate the cellular components and immunological characteristics of the head and neck rhabdomyosarcoma (RMS) microenvironment.
We conducted single-cell transcriptomics to analyze the cellular components of the RMS microenvironment. CellChat was utilized for analyzing intercellular interactions. The cancer genome atlas database was used for validation. CIBERSORT was applied for immune infiltration profiling. Functional enrichment analyses were performed using the Kyoto Encyclopedia of Genes and Genomes. Gene set scores were calculated using single-sample gene set enrichment analysis. Subcutaneous allograft models and bulk RNA sequencing were used for validation. Flow cytometry and immunohistochemistry were used to identify M2-like macrophages.
Our findings revealed an extremely low presence of neutrophils in RMS samples compared with normal sample. RMS sample with high Schwann cell infiltration exhibited an increase in M2-like macrophage infiltration. Receptor-ligand pairs, specifically MIF-CD74 and PTN-SDC3, were identified between Schwann cells and M2-like macrophages. In the RMS sample characterized by significant Schwann cell infiltration, M2-like macrophages demonstrate robust expression of axon guidance factors and are enriched in the axon guidance pathway.
Our study provides valuable insights into the microenvironment and immunological characteristics of RMS, offering crucial information for further research and potential therapeutic strategies.
探讨头颈部横纹肌肉瘤(RMS)微环境的细胞成分和免疫特征。
我们进行了单细胞转录组学分析以研究RMS微环境的细胞成分。利用CellChat分析细胞间相互作用。使用癌症基因组图谱数据库进行验证。应用CIBERSORT进行免疫浸润分析。使用京都基因与基因组百科全书进行功能富集分析。使用单样本基因集富集分析计算基因集分数。采用皮下异种移植模型和批量RNA测序进行验证。通过流式细胞术和免疫组织化学鉴定M2样巨噬细胞。
我们的研究结果显示,与正常样本相比,RMS样本中嗜中性粒细胞的含量极低。雪旺细胞浸润程度高的RMS样本中M2样巨噬细胞浸润增加。在雪旺细胞和M2样巨噬细胞之间鉴定出受体-配体对,特别是MIF-CD74和PTN-SDC3。在以显著雪旺细胞浸润为特征的RMS样本中,M2样巨噬细胞表现出轴突导向因子的强烈表达,并在轴突导向通路中富集。
我们的研究为RMS的微环境和免疫特征提供了有价值的见解,为进一步研究和潜在治疗策略提供了关键信息。