The SHH/GLI signaling pathway: a therapeutic target for medulloblastoma.
Animals
Antineoplastic Agents
/ pharmacology
Cerebellar Neoplasms
/ drug therapy
Hedgehog Proteins
/ metabolism
Humans
Immunotherapy
Medulloblastoma
/ drug therapy
Molecular Targeted Therapy
Signal Transduction
/ drug effects
Smoothened Receptor
/ antagonists & inhibitors
Zinc Finger Protein GLI1
/ antagonists & inhibitors
Cancer
drug discovery
gli
hedgehog pathway
immunotherapy
medulloblastoma
multitarget
small molecules
smo
therapeutic target
Journal
Expert opinion on therapeutic targets
ISSN: 1744-7631
Titre abrégé: Expert Opin Ther Targets
Pays: England
ID NLM: 101127833
Informations de publication
Date de publication:
11 2020
11 2020
Historique:
pubmed:
30
9
2020
medline:
22
4
2021
entrez:
29
9
2020
Statut:
ppublish
Résumé
Medulloblastoma (MB) is a heterogeneous tumor of the cerebellum that is divided into four main subgroups with distinct molecular and clinical features. Sonic Hedgehog MB (SHH-MB) is the most genetically understood and occurs predominantly in childhood. Current therapies consist of aggressive and non-targeted multimodal approaches that are often ineffective and cause long-term complications. These problems intensify the need to develop molecularly targeted therapies to improve outcome and reduce treatment-related morbidities. In this scenario, Hedgehog (HH) signaling, a developmental pathway whose deregulation is involved in the pathogenesis of several malignancies, has emerged as an attractive druggable pathway for SHH-MB therapy. This review provides an overview of the advancements in the HH antagonist research field. We place an emphasis on Smoothened (SMO) and glioma-associated oncogene homolog (GLI) inhibitors and immunotherapy approaches that are validated in preclinical SHH-MB models and that have therapeutic potential for MB patients. Literature from Pubmed and data reported on ClinicalTrial.gov up to August 2020 were considered. Extensive-omics analysis has enhanced our knowledge and has transformed the way that MB is studied and managed. The clinical use of SMO antagonists has yet to be determined, however, future GLI inhibitors and multitargeting approaches are promising.
Identifiants
pubmed: 32990091
doi: 10.1080/14728222.2020.1823967
doi:
Substances chimiques
Antineoplastic Agents
0
GLI1 protein, human
0
Hedgehog Proteins
0
SHH protein, human
0
SMO protein, human
0
Smoothened Receptor
0
Zinc Finger Protein GLI1
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM