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Single-cell RNA reveals a tumorigenic microenvironment in the interface zone of human breast tumors.
Yang, Wei; Xu, Meiyu; Xu, Shuoqi; Guan, Qingxian; Geng, Shuaiming; Wang, Juanhong; Wei, Wei; Xu, Hongwei; Liu, Ying; Meng, Yong; Gao, Ming-Qing.
Afiliación
  • Yang W; College of Life Sciences, Northwest University, Xi'an, China.
  • Xu M; College of Life Sciences, Northwest University, Xi'an, China.
  • Xu S; College of Life Sciences, Northwest University, Xi'an, China.
  • Guan Q; College of Life Sciences, Northwest University, Xi'an, China.
  • Geng S; College of Life Sciences, Northwest University, Xi'an, China.
  • Wang J; Department of Pathology, Xi'an No.3 Hospital, The Affiliated Hospital of Northwest University, Xi'an, China.
  • Wei W; Department of Pathology, Xi'an No.3 Hospital, The Affiliated Hospital of Northwest University, Xi'an, China.
  • Xu H; Basic Medical College, Qingdao University, Qingdao, China.
  • Liu Y; Basic Medical College, Qingdao University, Qingdao, China.
  • Meng Y; School of Medicine, Northwest University, Xi'an, China.
  • Gao MQ; School of Medicine, Northwest University, Xi'an, China. gaomingqing@nwu.edu.cn.
Breast Cancer Res ; 25(1): 100, 2023 08 29.
Article en En | MEDLINE | ID: mdl-37644609
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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias de la Mama / Carcinoma Tipo de estudio: Prognostic_studies Límite: Female / Humans Idioma: En Revista: Breast Cancer Res Asunto de la revista: NEOPLASIAS Año: 2023 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias de la Mama / Carcinoma Tipo de estudio: Prognostic_studies Límite: Female / Humans Idioma: En Revista: Breast Cancer Res Asunto de la revista: NEOPLASIAS Año: 2023 Tipo del documento: Article País de afiliación: China
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