Single-cell landscape of undifferentiated pleomorphic sarcoma.
Yifei LuDeqian ChenBingnan WangWenjun ChaiMingxia YanYong ChenYong ZhanRan YangEnqing ZhouShuyang DaiYi LiRui DongBiqiang ZhengPublished in: Oncogene (2024)
Undifferentiated pleomorphic sarcoma (UPS) is a highly aggressive malignant soft tissue tumor with a poor prognosis; however, the identity and heterogeneity of tumor populations remain elusive. Here, eight major cell clusters were identified through the RNA sequencing of 79,569 individual cells of UPS. UPS originates from mesenchymal stem cells (MSCs) and features undifferentiated subclusters. UPS subclusters were predicted to exist in two bulk RNA datasets, and had a prognostic value in The Cancer Genome Atlas (TCGA) dataset. The functional heterogeneity of malignant UPS cells and the immune microenvironment were characterized. Additionally, the fused cells were innovatively detected by expressing both monocyte/macrophage markers and other subcluster-associated genes. Based on the ligand-receptor interaction analysis, cellular interactions with epidermal growth factor receptor (EGFR) and vascular endothelial growth factor receptor (VEGFR) were abundant. Furthermore, 73% of patients with UPS (48/66) showed positive EGFR expression, which was associated with a poor prognosis. EGFR blockade with cetuximab inhibited tumor growth in a patient-derived xenograft model. Our transcriptomic studies delineate the landscape of UPS intratumor heterogeneity and serve as a foundational resource for further discovery and therapeutic exploration.
Keyphrases
- single cell
- poor prognosis
- epidermal growth factor receptor
- rna seq
- induced apoptosis
- long non coding rna
- high throughput
- vascular endothelial growth factor
- tyrosine kinase
- mesenchymal stem cells
- small cell lung cancer
- cell cycle arrest
- advanced non small cell lung cancer
- soft tissue
- cell death
- endoplasmic reticulum stress
- squamous cell carcinoma
- binding protein
- small molecule
- signaling pathway
- stem cells
- adipose tissue
- gene expression
- transcription factor
- umbilical cord
- pi k akt
- cell proliferation
- lymph node metastasis
- radiation therapy