单细胞RNA揭示了人乳腺肿瘤界面区致瘤微环境。

Wei Yang, Meiyu Xu, Shuoqi Xu, Qingxian Guan, Shuaiming Geng, Juanhong Wang, Wei Wei, Hongwei Xu, Ying Liu, Yong Meng, Ming-Qing Gao
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引用次数: 1

摘要

背景:浸润性癌周围的界面区可以被认为是肿瘤微环境的实际组织,肿瘤浸润有先前的改变。然而,界面区微环境的异质性和特征尚未得到彻底探索。方法:在体外研究中,使用单细胞RNA测序(scRNA-seq)来表征来自肿瘤区、正常区和界面区的细胞,肿瘤侵袭前沿和正常区之间有5毫米宽的带。通过scRNA-seq数据分析,我们比较了不同区域的细胞类型及其转录特征。进行假时间、细胞间通讯和通路分析以表征区域特异性微环境。细胞增殖、伤口愈合和克隆形成实验探索了差异表达基因BMPR1B的功能,并通过体内肿瘤模型证实了这一点。结果:筛选得到88548个优质细胞,并进行了鉴定。调节性T细胞、M2巨噬细胞、血管生成相关肥大细胞、DNA修复能力较弱的干细胞、具有血管生成活性的内皮细胞、具有胶原合成的成纤维细胞和具有增殖活性的上皮细胞在界面区形成独特的致瘤微环境。细胞通讯分析显示,与正常区相比,界面区不同细胞类型之间存在特殊的配体-受体对,可保护内皮细胞凋亡,促进上皮细胞增殖和迁移。与正常区相比,高表达的BMPR1B基因促进了癌症细胞在界面区的致瘤能力。结论:我们的工作确定了界面区独特的致瘤微环境,并使我们能够更深入地了解癌症的肿瘤微环境,这将为推进癌症的诊断和治疗提供有用的资源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Single-cell RNA reveals a tumorigenic microenvironment in the interface zone of human breast tumors.

Single-cell RNA reveals a tumorigenic microenvironment in the interface zone of human breast tumors.

Single-cell RNA reveals a tumorigenic microenvironment in the interface zone of human breast tumors.

Single-cell RNA reveals a tumorigenic microenvironment in the interface zone of human breast tumors.

Background: The interface zone, area around invasive carcinoma, can be thought of as the actual tissue of the tumor microenvironment with precedent alterations for tumor invasion. However, the heterogeneity and characteristics of the microenvironment in the interface area have not yet been thoroughly explored.

Methods: For in vitro studies, single-cell RNA sequencing (scRNA-seq) was used to characterize the cells from the tumor zone, the normal zone and the interface zone with 5-mm-wide belts between the tumor invasion front and the normal zone. Through scRNA-seq data analysis, we compared the cell types and their transcriptional characteristics in the different zones. Pseudotime, cell-cell communication and pathway analysis were performed to characterize the zone-specific microenvironment. Cell proliferation, wound healing and clone formation experiments explored the function of differentially expressed gene BMPR1B, which were confirmed by tumor models in vivo.

Results: After screening, 88,548 high-quality cells were obtained and identified. Regulatory T cells, M2 macrophages, angiogenesis-related mast cells, stem cells with weak DNA repair ability, endothelial cells with angiogenic activity, fibroblasts with collagen synthesis and epithelial cells with proliferative activity form a unique tumorigenic microenvironment in the interface zone. Cell-cell communication analysis revealed that there are special ligand-receptor pairs between different cell types in the interface zone, which protects endothelial cell apoptosis and promotes epithelial cell proliferation and migration, compared to the normal zone. Compared with the normal zone, the highly expressed BMPR1B gene promotes the tumorigenic ability of cancer cells in the interface zone.

Conclusions: Our work identified a unique tumorigenic microenvironment of the interface zone and allowed for deeper insights into the tumor microenvironment of breast cancer that will serve as a helpful resource for advancing breast cancer diagnosis and therapy.

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