Extracellular vesicles in neuroblastoma: role in progression, resistance to therapy and diagnostics.

Front Immunol

Division of Pediatric Hematology and Oncology, Department of Pediatrics, The Pennsylvania State University College of Medicine, Hershey, PA, United States.

Published: April 2024

AI Article Synopsis

  • Neuroblastoma (NB) is the most prevalent solid cancer in children and a leading cause of cancer-related fatalities, especially in advanced stages where treatment often fails.
  • Recent research has shed light on the role of small extracellular vesicles (EVs) in NB's progression, metastasis, and resistance to therapy, highlighting their increasingly recognized significance in the disease.
  • The review discusses findings on how EVs influence NB and explores potential strategies for targeting these vesicles therapeutically or using them as biomarkers for improved diagnosis and treatment.

Article Abstract

Neuroblastoma (NB) is the most common extracranial solid pediatric cancer, and is one of the leading causes of cancer-related deaths in children. Despite the current multi-modal treatment regimens, majority of patients with advanced-stage NBs develop therapeutic resistance and relapse, leading to poor disease outcomes. There is a large body of knowledge on pathophysiological role of small extracellular vesicles (EVs) in progression and metastasis of multiple cancer types, however, the importance of EVs in NB was until recently not well understood. Studies emerging in the last few years have demonstrated the involvement of EVs in various aspects of NB pathogenesis. In this review we summarize these recent findings and advances on the role EVs play in NB progression, such as tumor growth, metastasis and therapeutic resistance, that could be helpful for future investigations in NB EV research. We also discuss different strategies for therapeutic targeting of NB-EVs as well as utilization of NB-EVs as potential biomarkers.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11041043PMC
http://dx.doi.org/10.3389/fimmu.2024.1385875DOI Listing

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