A pan-cancer single-cell transcriptional analysis of antigen-presenting cancer-associated fibroblasts in the tumor microenvironment

被引:2
|
作者
Chen, Juntao [1 ]
Chen, Renhui [2 ]
Huang, Jingang [3 ]
机构
[1] Sun Yat Sen Univ, Shenshan Med Ctr, Mem Hosp, Shanwei, Peoples R China
[2] Sun Yat Sen Univ, Sun Yat Sen Mem Hosp, Med Res Ctr,Dept Otolaryngol Head & Neck Surg, Guangdong Prov Key Lab Malignant Tumor Epigenet &, Guangzhou, Peoples R China
[3] Sun Yat Sen Univ, Sun Yat Sen Mem Hosp, Med Res Ctr,Guangdong Hong Kong Joint Lab RNA Med, Guangdong Prov Key Lab Malignant Tumor Epigenet &, Guangzhou, Peoples R China
来源
FRONTIERS IN IMMUNOLOGY | 2024年 / 15卷
关键词
antigen-presenting CAFs; single-cell RNA-seq; cancer-associated fibroblasts; tumor microenvironment; CD4+effector T cells; C1Q molecules; EXPRESSION; REVEALS; GLUCOSE; ATLAS;
D O I
10.3389/fimmu.2024.1372432
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Cancer-associated fibroblasts (CAFs) are the primary stromal cells found in tumor microenvironment, and display high plasticity and heterogeneity. By using single-cell RNA-seq technology, researchers have identified various subpopulations of CAFs, particularly highlighting a recently identified subpopulation termed antigen-presenting CAFs (apCAFs), which are largely unknown. Methods: We collected datasets from public databases for 9 different solid tumor types to analyze the role of apCAFs in the tumor microenvironment. Results: Our data revealed that apCAFs, likely originating mainly from normal fibroblast, are commonly found in different solid tumor types and generally are associated with anti-tumor effects. apCAFs may be associated with the activation of CD4+ effector T cells and potentially promote the survival of CD4+ effector T cells through the expression of C1Q molecules. Moreover, apCAFs exhibited highly enrichment of transcription factors RUNX3 and IKZF1, along with increased glycolytic metabolism. Conclusions: Taken together, these findings offer novel insights into a deeper understanding of apCAFs and the potential therapeutic implications for apCAFs targeted immunotherapy in cancer.
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页数:22
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