Dynamic single-cell sequencing unveils the tumor microenvironment evolution of gastric cancer abdominal wall metastases during radiotherapy

被引:0
|
作者
Mao, Qianqian [1 ,2 ,3 ]
Wu, Zhenzhen [1 ]
Lai, Yonghong [1 ]
Wang, Ling [1 ]
Zhao, Qiongzhi [1 ]
Xu, Xi [1 ]
Lu, Xiansheng [4 ]
Qiu, Wenjun [1 ]
Zhang, Zhihua [1 ]
Wu, Jiani [1 ]
Wang, Gaofeng [1 ,5 ,6 ]
Zhou, Rui [1 ]
Wu, Jianhua [1 ]
Sun, Huiying [1 ]
Huang, Na [1 ]
Huang, Xiatong [1 ]
Jiang, Luyang [1 ]
Fang, Yiran [1 ]
Kong, Yuyun [1 ]
Liang, Li [4 ]
Bin, Jianping [7 ]
Liao, Yulin [7 ]
Shi, Min [1 ]
Liao, Wangjun [1 ,2 ,3 ]
Zeng, Dongqiang [1 ,2 ,3 ]
机构
[1] Nanfang Hosp, Dept Oncol, 1838 North Guangzhou Ave, Guangzhou 510515, Guangdong, Peoples R China
[2] South China Univ Technol, Affiliated Hosp 6, Canc Ctr, Sch Med, Foshan, Peoples R China
[3] South China Univ Technol, Affiliated Hosp 6, Sch Med, Foshan Key Lab Translat Med Oncol, Foshan, Peoples R China
[4] Southern Med Univ, Nanfang Hosp, Dept Pathol, Guangzhou, Guangdong, Peoples R China
[5] Southern Med Univ, Nanfang Hosp, Dept Plast & Aesthet Surg, Guangzhou, Guangdong, Peoples R China
[6] Johns Hopkins Univ, Sch Med, Dept Dermatol, Baltimore, MD USA
[7] Southern Med Univ, Nanfang Hosp, Dept Cardiol, Guangzhou, Guangdong, Peoples R China
关键词
gastric cancer; immunomodulation; radiotherapy; single cell sequence; tumor microenvironment; ATLAS;
D O I
10.1111/cas.16308
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Although the combination of immunotherapy and radiotherapy (RT) for the treatment of malignant tumors has shown rapid development, the insight of how RT remodels the tumor microenvironment to prime antitumor immunity involves a complex interplay of cell types and signaling pathways, much of which remains to be elucidated. Four tumor samples were collected from the same abdominal wall metastasis site of the patient with gastric cancer at baseline and during fractionated RT for single-cell RNA and T-cell receptor sequencing. The Seurat analysis pipeline and immune receptor analysis were used to characterize the gastric cancer metastasis ecosystem and investigated its dynamic changes of cell proportion, cell functional profiles and cell-to-cell communication during RT. Immunohistochemical and immunofluorescent staining and bulk RNA sequencing were applied to validate the key results. We found tumor cells upregulated immune checkpoint genes in response to RT. The infiltration and clonal expansion of T lymphocytes declined within tumors undergoing irradiation. Moreover, RT led to the accumulation of proinflammatory macrophages and natural killer T cells with enhanced cytotoxic gene expression signature. In addition, subclusters of dendritic cells and endothelial cells showed decrease in the expression of antigen present features in post-RT samples. More ECM component secreted by myofibroblasts during RT. These findings indicate that RT induced the dynamics of the immune response that should be taken into consideration when designing and clinically implementing innovative multimodal cancer treatment regimens of different RT and immunotherapy approaches. The study characterized the gastric cancer abdominal wall metastasis ecosystem and investigated its dynamic changes of cell proportion, cell functional profiles, and cell-to-cell communication as well as T cell repertoire during radiotherapy.image
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页数:16
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