A Perspective on the CD47-SIRPA Axis in High-Risk Neuroblastoma.
CD47
GD2
SIRPA
SLAMF7
high-risk neuroblastoma
immunotherapy
macrophages
Journal
Current oncology (Toronto, Ont.)
ISSN: 1718-7729
Titre abrégé: Curr Oncol
Pays: Switzerland
ID NLM: 9502503
Informations de publication
Date de publication:
01 Jun 2024
01 Jun 2024
Historique:
received:
03
05
2024
revised:
29
05
2024
accepted:
31
05
2024
medline:
26
6
2024
pubmed:
26
6
2024
entrez:
26
6
2024
Statut:
epublish
Résumé
Neuroblastoma is a pediatric cancer with significant clinical heterogeneity. Despite extensive efforts, it is still difficult to cure children with high-risk neuroblastoma. Immunotherapy is a promising approach to treat children with this devastating disease. We have previously reported that macrophages are important effector cells in high-risk neuroblastoma. In this perspective article, we discuss the potential function of the macrophage inhibitory receptor SIRPA in the homeostasis of tumor-associated macrophages in high-risk neuroblastoma. The ligand of SIRPA is CD47, known as a "don't eat me" signal, which is highly expressed on cancer cells compared to normal cells. CD47 is expressed on both tumor and stroma cells, whereas SIRPA expression is restricted to macrophages in high-risk neuroblastoma tissues. Notably, high
Identifiants
pubmed: 38920727
pii: curroncol31060243
doi: 10.3390/curroncol31060243
doi:
Substances chimiques
CD47 Antigen
0
Receptors, Immunologic
0
SIRPA protein, human
0
Antigens, Differentiation
0
CD47 protein, human
0
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM