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A Comparison of in vivo Tumor-Homing Abilities of Placental-Derived and Bone Marrow-Derived Mesenchymal Stromal Cells in High-Risk Neuroblastoma
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Pediatric Oncology 696 items
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Read the article on jpedsurg.org ↗Article · Sep 2024 · 1 min read
In brief
In brief
This study evaluates placental-derived versus bone marrow-derived mesenchymal stromal cells as potential cellular delivery vehicles for treating high-risk neuroblastoma in children. Using an orthotopic xenograft model, researchers compared the tumor-homing capabilities of both MSC types to determine which shows superior targeting for future therapeutic applications.
- Mesenchymal stromal cells possess innate tumor-homing properties that may enable targeted cellular therapy delivery in neuroblastoma
- Placental-derived MSCs and bone marrow-derived MSCs were compared for tumor-homing efficacy in orthotopic neuroblastoma models
- MSC-based delivery vehicles represent a novel therapeutic approach for high-risk neuroblastoma in pediatric patients
Written by the GCMD Library team from the article.
Neuroblastoma is a highly lethal malignancy of young children. Mesenchymal stromal cells (MSCs) may represent a novel cellular delivery vehicle due to their innate tumor-homing properties. We compared in vivo homing abilities of placental-derived MSCs (PMSCs) and bone marrow-derived MSCs (BM-MSCs) in an orthotopic neuroblastoma xenograft.
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