Related Experiment Video
Updated: May 22, 2025

Three-Dimensional Bone Extracellular Matrix Model for Osteosarcoma
Published on: April 12, 2019
Thrombospondin 1 Promotes Cytoskeleton Remodeling, Dedifferentiation, and Pulmonary Metastasis through ITGA1 and
Enjie Xu1,2, Zhen Huang1,2, Kunpeng Zhu1,2
1Department of Orthopedic Surgery, Shanghai Tenth People's Hospital, School of Medicine, Tongji University, Shanghai, 200072, PR China.
Abstract:
Dedifferentiation of osteosarcoma cells leads to poor prognosis. We plan to identify the key molecules that are involved in cell dedifferentiation and explore how they promote the pulmonary metastasis of osteosarcoma cells. We performed a sphere formation assay and confirmed that the spheroid cells could be redifferentiated into osteoblasts, adipocytes, and chondrocytes in specific medium, and the stem cell-like markers Stro-1 and CD117 were detected on the cell surface, which indicated that the spheroid cells were dedifferentiated cells. Thrombospondin 1 (THBS1) and ITGAs were identified as the key molecules in dedifferentiation through mRNA-seq and analysis, and osteosarcoma patients with higher THBS1 expression had a worse prognosis than those with lower THBS1 expression. THBS1 promotes the accumulation of ITGA1 and ITGA6 on the cell membrane in the early phase of dedifferentiation, thereby increasing the phosphorylation of FAK, RasGRF1, and MLC2 in the cytoplasm and promoting cytoskeleton remodeling. Our results suggest that THBS1 promotes cell dedifferentiation and pulmonary metastasis by promoting cytoskeletal remodeling and that ITGA1 and ITGA6 play important roles in mediating extracellular to intracellular signals; this mediating effect takes place mainly in the early phase of dedifferentiation.
Insights
Thrombospondin 1 (THBS1) drives osteosarcoma cell dedifferentiation and metastasis by promoting cytoskeletal remodeling. This involves ITGA1 and ITGA6, crucial for early-stage signal mediation, impacting patient prognosis.
Area of Science:
- Oncology
- Cell Biology
- Biochemistry
Background:
- Osteosarcoma cell dedifferentiation is linked to poor patient prognosis.
- Identifying key molecules in dedifferentiation is crucial for understanding and targeting pulmonary metastasis.
Purpose of the Study:
- To identify key molecules involved in osteosarcoma cell dedifferentiation.
- To investigate the role of these molecules in promoting pulmonary metastasis.
Main Methods:
- Sphere formation assay to generate and identify dedifferentiated cells.
- mRNA sequencing (mRNA-seq) and bioinformatic analysis to identify key molecules.
- Western blotting or similar techniques to analyze protein phosphorylation and signaling pathways.
Main Results:
- Spheroid cells exhibited stem cell-like markers (Stro-1, CD117) and redifferentiation capacity.
- Thrombospondin 1 (THBS1) and Integrins alpha 1/6 (ITGA1/ITGA6) were identified as key molecules.
- Higher THBS1 expression correlated with worse prognosis in osteosarcoma patients.
- THBS1 promotes ITGA1/ITGA6 accumulation, leading to FAK/RasGRF1/MLC2 phosphorylation and cytoskeleton remodeling.
Conclusions:
- THBS1 promotes osteosarcoma cell dedifferentiation and pulmonary metastasis via cytoskeletal remodeling.
- ITGA1 and ITGA6 mediate extracellular-to-intracellular signaling during early dedifferentiation.
More Related Videos
Related Concept Videos
Intracellular Signaling Affects Focal Adhesions
Some...
Destabilization of Microtubules
Metastasis
Epithelial-to-Mesenchymal Transition
The epithelial-to-mesenchymal transition or EMT is a developmental process commonly observed in wound healing, embryogenesis, and cancer metastasis. EMT is induced by transforming growth factor-beta (TGF-β) or receptor tyrosine kinase (RTK) ligands, which further...
Cytoskeletal Coordination in Cell Migration
Cancer Cell Migration through Invadopodia
TGF - β Signaling Pathway

