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Updated: Jan 20, 2026

Induction of Mesenchymal-Epithelial Transitions in Sarcoma Cells
Published on: April 7, 2017
The Tumor Microenvironment of Pediatric Sarcoma: Mesenchymal Mechanisms Regulating Cell Migration and Metastasis
Monika Ehnman1,2, Wiem Chaabane3,4, Felix Haglund3
1Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden. monika.ehnman@ki.se.
Purpose Of Review:
This review presents a selection of regulatory molecules of tumor microenvironmental properties and metastasis. Signaling pathways controlling mesenchymal biology in bone and soft-tissue sarcomas found in children and adolescents are prioritized.
Recent Findings:
The tumor microenvironment of pediatric tumors is still relatively unexplored. Highlighted findings are mainly on deregulated genes associated with cell adhesion, migration, and tumor cell dissemination. How these processes are involved in a mesenchymal phenotype and metastasis is further discussed in relation to the epithelial to mesenchymal transition (EMT) in epithelial tumors. Cell plasticity is emerging as a concept with impact on tumor behavior. Sarcomas belong to a heterogeneous group of tumors where local recurrence and tumor spread pose major challenges despite intense multimodal treatments. Molecular pathways involved in the metastatic process are currently being characterized, and tumor-regulatory properties of structural components, and infiltrating, non-malignant cell types should be further investigated.
Insights
This review explores tumor microenvironment and metastasis in pediatric sarcomas. It highlights molecular pathways controlling cell plasticity and mesenchymal biology, crucial for understanding tumor spread.
Area of Science:
- Pediatric Oncology
- Cancer Metastasis
- Tumor Microenvironment
- Molecular Biology
Background:
- The tumor microenvironment in pediatric cancers remains under-researched.
- Pediatric sarcomas are a heterogeneous group of tumors presenting significant treatment challenges, including local recurrence and metastasis.
Purpose of the Study:
- To review regulatory molecules influencing tumor microenvironmental properties and metastasis in pediatric sarcomas.
- To prioritize signaling pathways governing mesenchymal biology in pediatric bone and soft-tissue sarcomas.
Main Methods:
- Review of current literature on tumor microenvironment and metastasis in pediatric sarcomas.
- Analysis of deregulated genes related to cell adhesion, migration, and dissemination.
- Discussion of mesenchymal phenotype and its relation to epithelial to mesenchymal transition (EMT).
Main Results:
- Identified key deregulated genes involved in cell adhesion, migration, and tumor cell dissemination.
- Explored the role of cell plasticity in pediatric tumor behavior and metastasis.
- Discussed the involvement of mesenchymal biology in pediatric sarcomas and its link to metastasis.
Conclusions:
- Understanding molecular pathways in pediatric sarcoma metastasis is critical.
- Further investigation into tumor-regulatory properties of non-malignant cells and structural components is warranted.
- Cell plasticity is an emerging concept impacting pediatric tumor behavior and treatment strategies.
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