Hopes on immunotherapy targeting B7-H3 in neuroblastoma.
B7-H3
CAR therapy
CD276
Immune checkpoint protein
Immunotherapy
Neuroblastoma
Journal
Translational oncology
ISSN: 1936-5233
Titre abrégé: Transl Oncol
Pays: United States
ID NLM: 101472619
Informations de publication
Date de publication:
Jan 2023
Jan 2023
Historique:
received:
20
08
2022
revised:
29
09
2022
accepted:
25
10
2022
pubmed:
4
11
2022
medline:
4
11
2022
entrez:
3
11
2022
Statut:
ppublish
Résumé
Neuroblastoma is one of the most aggressive cancer forms in children, with highly heterogenous clinical manifestations ranging from spontaneous regression to high metastatic capacity. High-risk neuroblastoma has the highest mortality rates of all pediatric cancers, highlighting the urgent need for effective novel therapeutic interventions. B7-H3 immune checkpoint protein is highly expressed in neuroblastoma, and it is involved in oncogenic signaling, tumor cell plasticity, and drug resistance. Immunotherapies based on immune checkpoint inhibition have improved patient survival in several human cancers, and recent reports provide preclinical evidence on the benefits of targeting B7-H3 in neuroblastoma, with emphasis on novel CAR T/NK-cell approaches. Here, we summarize the current status of neuroblastoma targeted therapies, with a focus on B7-H3 as a promising novel immunoregulatory therapeutic target for high-risk neuroblastoma.
Identifiants
pubmed: 36327699
pii: S1936-5233(22)00239-X
doi: 10.1016/j.tranon.2022.101580
pmc: PMC9636568
pii:
doi:
Types de publication
Journal Article
Langues
eng
Pagination
101580Informations de copyright
Copyright © 2022. Published by Elsevier Inc.
Déclaration de conflit d'intérêts
Declaration of Competing Interest The authors declare no conflict of interest.