Distinct immune microenvironment of lung adenocarcinoma in never-smokers from smokers

被引:12
|
作者
Luo, Wenxin [1 ]
Zeng, Zhen [2 ,3 ]
Jin, Yang [1 ,2 ,3 ]
Yang, Lan
Fan, Ting [2 ,3 ]
Wang, Zhoufeng [4 ]
Pan, Yitong [2 ,3 ,4 ]
Yang, Ying [4 ]
Yao, Menglin [4 ]
Li, Yangqian [4 ]
Xiao, Xue [4 ]
Wang, Gang [4 ]
Wang, Chengdi [1 ]
Chang, Shuai [5 ]
Che, Guowei [5 ]
Zhang, Li [4 ]
Li, Yalun [1 ]
Peng, Yong [2 ,3 ]
Li, Weimin [1 ]
机构
[1] Sichuan Univ, West China Hosp, Dept Resp & Crit Care Med, Inst Resp Hlth,Precis Med Ctr,Precis Med Key Lab S, Chengdu 610041, Peoples R China
[2] Sichuan Univ, Canc Ctr, Lab Mol Oncol, West China Hosp,Dept Biotherapy,Frontiers Sci Ctr, Chengdu 610041, Peoples R China
[3] Sichuan Univ, West China Hosp, State Key Lab Biotherapy, Chengdu 610041, Peoples R China
[4] Sichuan Univ, Precis Med Key Lab Sichuan Prov, Frontiers Sci Ctr Dis Related Mol Network, Precis Med Ctr,West China Hosp, Chengdu 610041, Peoples R China
[5] Sichuan Univ, West China Hosp, Dept Thorac Surg, Chengdu 610041, Peoples R China
基金
中国国家自然科学基金;
关键词
MHC CLASS-I; COLORECTAL-CANCER; TISSUE-RESIDENT; CELLS; MACROPHAGES; CLASSIFICATION; EXPRESSION; LANDSCAPE;
D O I
10.1016/j.xcrm.2023.101078
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Lung cancer in never-smokers (LCINS) presents clinicopathological and molecular features distinct from that in smokers. Tumor microenvironment (TME) plays important roles in cancer progression and therapeutic response. To decipher the difference in TME between never-smoker and smoker lung cancers, we conduct single-cell RNA sequencing on 165,753 cells from 22 treatment-naive lung adenocarcinoma (LUAD) patients. We find that the dysfunction of alveolar cells induced by cigarette smoking contributes more to the aggres-siveness of smoker LUADs, while the immunosuppressive microenvironment exerts more effects on never -smoker LUADs' aggressiveness. Moreover, the SPP1hi pro macrophage is identified to be another indepen-dent source of monocyte-derived macrophage. Importantly, higher expression of immune checkpoint CD47 and lower expression of major histocompatibility complex (MHC)-I in cancer cells of never-smoker LUADs imply that CD47 may be a better immunotherapy target for LCINS. Therefore, this study reveals the difference of tumorigenesis between never-smoker and smoker LUADs and provides a potential immunotherapy strat-egy for LCINS.
引用
收藏
页数:24
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