TY - JOUR
T1 - BRAF and MEK Targeted Therapies in Pediatric Central Nervous System Tumors
AU - Talloa, D.
AU - Triarico, S.
AU - Agresti, P.
AU - Mastrangelo, Stefano
AU - Attina, G.
AU - Romano, A.
AU - Maurizi, Palma
AU - Ruggiero, Antonio
PY - 2022
Y1 - 2022
N2 - BRAF is a component of the MAPK and PI3K/AKT/mTOR pathways that play a crucial role in cellular proliferation, differentiation, migration, and angiogenesis. Pediatric central nervous system tumors very often show mutations of the MAPK pathway, as demonstrated by next-generation sequencing (NGS), which now has an increasing role in cancer diagnostics. The MAPK mutated pathway in pediatric CNS tumors is the target of numerous drugs, approved or under investigation in ongoing clinical trials. In this review, we describe the main aspects of MAPK and PI3K/AKT/mTOR signaling pathways, with a focus on the alterations commonly involved in tumorigenesis. Furthermore, we reported the main available data about current BRAF and MEK targeted therapies used in pediatric low-grade gliomas (pLLGs), pediatric high-grade gliomas (pHGGs), and other CNS tumors that often present BRAF or MEK mutations. Further molecular stratification and clinical trial design are required for the treatment of pediatric CNS tumors with BRAF and MEK inhibitors.
AB - BRAF is a component of the MAPK and PI3K/AKT/mTOR pathways that play a crucial role in cellular proliferation, differentiation, migration, and angiogenesis. Pediatric central nervous system tumors very often show mutations of the MAPK pathway, as demonstrated by next-generation sequencing (NGS), which now has an increasing role in cancer diagnostics. The MAPK mutated pathway in pediatric CNS tumors is the target of numerous drugs, approved or under investigation in ongoing clinical trials. In this review, we describe the main aspects of MAPK and PI3K/AKT/mTOR signaling pathways, with a focus on the alterations commonly involved in tumorigenesis. Furthermore, we reported the main available data about current BRAF and MEK targeted therapies used in pediatric low-grade gliomas (pLLGs), pediatric high-grade gliomas (pHGGs), and other CNS tumors that often present BRAF or MEK mutations. Further molecular stratification and clinical trial design are required for the treatment of pediatric CNS tumors with BRAF and MEK inhibitors.
KW - BRAF
KW - MEK
KW - NGS
KW - central nervous system (CNS) tumors
KW - children
KW - targeted therapies
KW - BRAF
KW - MEK
KW - NGS
KW - central nervous system (CNS) tumors
KW - children
KW - targeted therapies
UR - https://publicatt.unicatt.it/handle/10807/223514
UR - https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85137814168&origin=inward
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85137814168&origin=inward
U2 - 10.3390/cancers14174264
DO - 10.3390/cancers14174264
M3 - Article
SN - 2072-6694
VL - 14
SP - N/A-N/A
JO - Cancers
JF - Cancers
IS - 17
ER -