Liu Bing, Wang Chen, Fang Zhanjie, Bai Jing, Qian Ying, Ma Yuanyuan, Ruan Xiuyan, Yan Shi, Li Shaolei, Wang Yaqi, Dong Bin, Yang Xin, Li Meng, Xia Xuefeng, Qu Hongzhu, Fang Xiangdong, Wu Nan
Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Thoracic Surgery II, Peking University Cancer Hospital & Institute, Beijing, China.
CAS Key Laboratory of Genome Sciences and Information, Beijing Key Laboratory of Genome and Precision Medicine Technologies, Beijing Institute of Genomics, Chinese Academy of Sciences/China National Center for Bioinformation, Beijing, China.
Front Cell Dev Biol. 2022 Aug 15;10:927300. doi: 10.3389/fcell.2022.927300. eCollection 2022.
Pure ground glass nodules (GGNs) and solid nodules (SNs) represent early and relatively late stages of lung adenocarcinoma (LUAD) in radiology, respectively. The cellular and molecular characteristics of pure GGNs and SNs have not been comprehensively elucidated. Additionally, the mechanism driving the progression of lung adenocarcinoma from pure GGN to SN in radiology is also elusive. In this study, by analyzing the single-cell transcriptomic profiles of 76,762 cells from four pure GGNs, four SNs, and four normal tissues, we found that anti-tumor immunity mediated by NK and CD8+T cells gradually weakened with the progression of LUAD and humoral immunity mediated by plasma B cells was more active in SNs. Additionally, the proliferation ability of some special epithelial cell increased during the progression process from pure GGN to SN. Furthermore, stromal cells and M2 macrophages could assist the progression of LUAD. Through comprehensive analyses, we revealed dynamic changes in cellular components and intercellular interactions during the progression of LUAD. These findings could facilitate our understanding of LUAD and discovery of novel therapeutic targets.
纯磨玻璃结节(GGNs)和实性结节(SNs)在放射学上分别代表肺腺癌(LUAD)的早期和相对晚期阶段。纯GGNs和SNs的细胞和分子特征尚未得到全面阐明。此外,放射学上驱动肺腺癌从纯GGN进展为SN的机制也尚不明确。在本研究中,通过分析来自四个纯GGN、四个SN和四个正常组织的76762个细胞的单细胞转录组图谱,我们发现由自然杀伤细胞(NK)和CD8+T细胞介导的抗肿瘤免疫随着LUAD的进展逐渐减弱,而由浆B细胞介导的体液免疫在SN中更活跃。此外,一些特殊上皮细胞的增殖能力在从纯GGN到SN的进展过程中有所增加。此外,基质细胞和M2巨噬细胞可促进LUAD的进展。通过综合分析,我们揭示了LUAD进展过程中细胞成分和细胞间相互作用的动态变化。这些发现有助于我们对LUAD的理解和发现新的治疗靶点。