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单细胞 RNA 揭示了人类乳腺肿瘤界面区的肿瘤微环境。

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

机构信息

College of Life Sciences, Northwest University, Xi'an, China.

Department of Pathology, Xi'an No.3 Hospital, The Affiliated Hospital of Northwest University, Xi'an, China.

出版信息

Breast Cancer Res. 2023 Aug 29;25(1):100. doi: 10.1186/s13058-023-01703-7.

Abstract

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.

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,具有肿瘤侵袭的先前改变。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) 对肿瘤区、正常区和肿瘤侵袭前缘与正常区之间有 5-mm 宽带的界面区的细胞进行特征描述。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。进行拟时分析、细胞间通讯和通路分析,以描述特定区域的微环境。通过细胞增殖、伤口愈合和克隆形成实验探索差异表达基因 BMPR1B 的功能,并用体内肿瘤模型进行了验证。

结果

筛选后获得并鉴定了 88548 个高质量细胞。调节性 T 细胞、M2 巨噬细胞、与血管生成相关的肥大细胞、具有弱 DNA 修复能力的干细胞、具有血管生成活性的内皮细胞、具有胶原合成能力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肿瘤发生微环境。细胞间通讯分析表明,界面区不同细胞类型之间存在特殊的配体-受体对,与正常区相比,这些配体-受体对可保护内皮细胞凋亡,并促进上皮细胞增殖和迁移。与正常区相比,高表达的 BMPR1B 基因促进了界面区癌细胞的肿瘤发生能力。

结论

我们的工作确定了界面区独特的肿瘤发生微环境,并深入了解了乳腺癌的肿瘤微环境,这将有助于推进乳腺癌的诊断和治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef78/10463980/377368acb860/13058_2023_1703_Fig1_HTML.jpg

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