Endothelial Cells Potentially Participate in the Metastasis of Triple-Negative Breast Cancer
Yanfei Ma1,2,3, Yanghong Li2,3, Pengwei Guo2,4
1Jinan University, Guangzhou, Guangdong Province, China.
Abstract:
Inhibition of triple-negative breast cancer metastasis has long been a challenge, mainly due to the difficulty in identifying factors that contribute to this process. In this study, freshly isolated triple-negative breast cancer biopsied cells obtained from consenting patients were subjected to flow cytometry and bioinformatic analysis to identify three endothelial cell subclusters: EC (ATP1B3), EC (HSPA1B), and EC (KRT7) in the tumor microenvironment. These endothelial cell subclusters exhibited distinguishing biological features. Based on differentially expressed genes derived from the subclusters, gene set enrichment analysis showed that EC (ATP1B3) and EC (HSPA1B) contribute to the process of metastasis, for example, in fibrosarcoma and anaplastic carcinoma. In this study, we identified the heterogeneity of endothelial cells in the human breast cancer and have provided insights into its role in metastasis.
Insights
Researchers identified distinct endothelial cell subclusters in triple-negative breast cancer. Certain subclusters, EC (ATP1B3) and EC (HSPA1B), are linked to cancer metastasis, offering new insights into tumor progression.
Area of Science:
- Oncology
- Cell Biology
- Cancer Research
Background:
- Triple-negative breast cancer (TNBC) metastasis is difficult to inhibit due to unidentified contributing factors.
- Understanding the tumor microenvironment is crucial for developing effective anti-metastatic strategies.
Purpose of the Study:
- To identify and characterize endothelial cell heterogeneity within the TNBC tumor microenvironment.
- To investigate the role of specific endothelial cell subclusters in promoting cancer metastasis.
Main Methods:
- Freshly isolated TNBC biopsy cells from consenting patients were analyzed.
- Flow cytometry and bioinformatic analyses were employed to identify endothelial cell subclusters.
- Gene set enrichment analysis was performed on differentially expressed genes.
Main Results:
- Three distinct endothelial cell subclusters were identified: EC (ATP1B3), EC (HSPA1B), and EC (KRT7).
- EC (ATP1B3) and EC (HSPA1B) subclusters demonstrated biological features associated with metastasis.
- These subclusters showed enrichment in pathways related to fibrosarcoma and anaplastic carcinoma metastasis.
Conclusions:
- Endothelial cell heterogeneity exists within human breast cancer.
- Specific endothelial cell subclusters, EC (ATP1B3) and EC (HSPA1B), play a role in promoting cancer metastasis.
- These findings provide novel insights into the mechanisms of TNBC metastasis.
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