Single-Cell Transcriptomic Profiles of Lung Pre-Metastatic Niche Reveal Neutrophil and Lymphatic Endothelial Cell Roles in Breast Cancer.
Yung-Chi HuangChao-Yuan ChangYu-Yuan WuKuan-Li WuYing-Ming TsaiHsiao-Chen LeeEing-Mei TsaiYa-Ling HsuPublished in: Cancers (2022)
The establishment of a pre-metastatic niche (PMN) is critical for cancer metastasis. However, it remains unclear as to which phenotypes induce changes in the PMN. Single-cell transcriptomic profiling of all cells of the lung in cancer-bearing MMTV-PyVT mice revealed an increased infiltration of N2-type neutrophils and classical monocytes associated with chronic inflammation; notably, lung neutrophils isolated from mice with primary cancer exhibited similar N2-type phenotypes and expressed high levels of inflammatory and angiogenic factors. We also discovered a new cluster of Ki67-upregulated lymphatic endothelial cells (ECs) that activated several cell division-related pathways. Receptor-ligand interactions within the lung potentially mediated PMN formation; these were exemplified by the cross talk of lymphatic EC-N2-type neutrophil via S100A6. In vitro study revealed S100A6 impaired EC tight junction and increased the transendothelial migration of neutrophils. Our results highlight the molecular mechanisms that shape lung PMN and inspire preventive strategies for lung metastasis in breast cancer.
Keyphrases
- single cell
- rna seq
- endothelial cells
- papillary thyroid
- high throughput
- lymph node
- squamous cell
- oxidative stress
- induced apoptosis
- mesenchymal stem cells
- type diabetes
- stem cells
- gene expression
- lymph node metastasis
- childhood cancer
- bone marrow
- young adults
- dna methylation
- peripheral blood
- insulin resistance
- endoplasmic reticulum stress
- binding protein
- skeletal muscle
- cell proliferation
- pi k akt