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Fusion Oncoproteins in Childhood Cancers: Potential Role in Targeted Therapy.

Authors :
Angione SDA
Akalu AY
Gartrell J
Fletcher EP
Burckart GJ
Reaman GH
Leong R
Stewart CF
Source :
The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG [J Pediatr Pharmacol Ther] 2021; Vol. 26 (6), pp. 541-555. Date of Electronic Publication: 2021 Aug 16.
Publication Year :
2021

Abstract

Cancer remains the leading cause of death from disease in children. Historically, in contrast to their adult counterparts, the causes of pediatric malignancies have remained largely unknown, with most pediatric cancers displaying low mutational burdens. Research related to molecular genetics in pediatric cancers is advancing our understanding of potential drivers of tumorigenesis and opening new opportunities for targeted therapies. One such area is fusion oncoproteins, which are a product of chromosomal rearrangements resulting in the fusion of different genes. They have been identified as oncogenic drivers in several sarcomas and leukemias. Continued advancement in the understanding of the biology of fusion oncoproteins will contribute to the discovery and development of new therapies for childhood cancers. Here we review the current scientific knowledge on fusion oncoproteins, focusing on pediatric sarcomas and hematologic cancers, and highlight the challenges and current efforts in developing drugs to target fusion oncoproteins.<br />Competing Interests: Disclosures. The author(s) declare no conflicts or financial interest in any product or service mentioned in the manuscript, including grants, equipment, medications, employment, gifts, and honoraria.<br /> (Copyright. Pediatric Pharmacy Association. All rights reserved. For permissions, email: mhelms@pediatricpharmacy.org 2021.)

Details

Language :
English
ISSN :
1551-6776
Volume :
26
Issue :
6
Database :
MEDLINE
Journal :
The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG
Publication Type :
Academic Journal
Accession number :
34421403
Full Text :
https://doi.org/10.5863/1551-6776-26.6.541