TY - JOUR
T1 - Reimagining pilocytic astrocytomas in the context of pediatric low-grade gliomas
AU - Milde, Till
AU - Rodriguez, Fausto J.
AU - Barnholtz-Sloan, Jill S.
AU - Patil, Nirav
AU - Eberhart, Charles G.
AU - Gutmann, David H.
N1 - Publisher Copyright:
© 2021 The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. All rights reserved. For permissions, please e-mail: [email protected].
PY - 2021/10/1
Y1 - 2021/10/1
N2 - Pediatric low-grade gliomas (pLGGs) are the most common brain tumor in children and are associated with lifelong clinical morbidity. Relative to their high-grade adult counterparts or other malignant childhood brain tumors, there is a paucity of authenticated preclinical models for these pLGGs and an incomplete understanding of their molecular and cellular pathogenesis. While large-scale genomic profiling efforts have identified the majority of pathogenic driver mutations, which converge on the MAPK/ERK signaling pathway, it is now appreciated that these events may not be sufficient by themselves for gliomagenesis and clinical progression. In light of the recent World Health Organization reclassification of pLGGs, and pilocytic astrocytoma (PA), in particular, we review our current understanding of these pediatric brain tumors, provide a conceptual framework for future mechanistic studies, and outline the challenges and pressing needs for the pLGG clinical and research communities.
AB - Pediatric low-grade gliomas (pLGGs) are the most common brain tumor in children and are associated with lifelong clinical morbidity. Relative to their high-grade adult counterparts or other malignant childhood brain tumors, there is a paucity of authenticated preclinical models for these pLGGs and an incomplete understanding of their molecular and cellular pathogenesis. While large-scale genomic profiling efforts have identified the majority of pathogenic driver mutations, which converge on the MAPK/ERK signaling pathway, it is now appreciated that these events may not be sufficient by themselves for gliomagenesis and clinical progression. In light of the recent World Health Organization reclassification of pLGGs, and pilocytic astrocytoma (PA), in particular, we review our current understanding of these pediatric brain tumors, provide a conceptual framework for future mechanistic studies, and outline the challenges and pressing needs for the pLGG clinical and research communities.
KW - BRAF
KW - MEK
KW - cellular senescence
KW - low-grade glioma
KW - neurofibromatosis type 1
KW - pediatric brain tumor
KW - pilocytic astrocytoma
KW - tumor microenvironment
UR - http://www.scopus.com/inward/record.url?scp=85117415127&partnerID=8YFLogxK
U2 - 10.1093/neuonc/noab138
DO - 10.1093/neuonc/noab138
M3 - Article
C2 - 34131743
AN - SCOPUS:85117415127
SN - 1522-8517
VL - 23
SP - 1634
EP - 1646
JO - Neuro-oncology
JF - Neuro-oncology
IS - 10
ER -