The Tumor Microenvironment of Pediatric Sarcoma: Mesenchymal Mechanisms Regulating Cell Migration and Metastasis

Curr Oncol Rep. 2019 Aug 15;21(10):90. doi: 10.1007/s11912-019-0839-6.

Abstract

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.

Keywords: CXCR4; EMT; Ewing sarcoma; Extracellular matrix; MET; Metastasis; Osteosarcoma; PDGF; Pediatric sarcoma; Rhabdomyosarcoma; Stroma; TGFβ; Tumor microenvironment.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Cell Movement / physiology
  • Child
  • Epithelial-Mesenchymal Transition
  • Humans
  • Neoplasm Metastasis
  • Sarcoma / immunology
  • Sarcoma / pathology*
  • Signal Transduction
  • Tumor Microenvironment