A Perspective on the CD47-SIRPA Axis in High-Risk Neuroblastoma.


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
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

Pagination

3212-3226

Auteurs

Xao X Tang (XX)

Department of Anatomy and Cell Biology, College of Medicine, University of Illinois at Chicago, Chicago, IL 60612, USA.

Hiroyuki Shimada (H)

Departments of Pathology and Pediatrics, School of Medicine, Stanford University, Stanford, CA 94305, USA.

Naohiko Ikegaki (N)

Department of Anatomy and Cell Biology, College of Medicine, University of Illinois at Chicago, Chicago, IL 60612, USA.

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Classifications MeSH