The Power of Human Cancer Genetics as Revealed by Low-Grade Gliomas.
Adult
Age Factors
Brain
/ growth & development
Brain Neoplasms
/ diagnosis
Child
Glioma
/ diagnosis
High-Throughput Nucleotide Sequencing
Humans
Isocitrate Dehydrogenase
/ genetics
Molecular Diagnostic Techniques
Mutation
Neurodevelopmental Disorders
/ genetics
Receptor, Fibroblast Growth Factor, Type 1
/ genetics
raf Kinases
/ genetics
BRAF
DNA methylation
IDH
development
low-grade gliomas
next-generation sequencing
pediatric
Journal
Annual review of genetics
ISSN: 1545-2948
Titre abrégé: Annu Rev Genet
Pays: United States
ID NLM: 0117605
Informations de publication
Date de publication:
03 12 2019
03 12 2019
Historique:
entrez:
4
12
2019
pubmed:
4
12
2019
medline:
9
7
2020
Statut:
ppublish
Résumé
The human brain contains a vast number of cells and shows extraordinary cellular diversity to facilitate the many cognitive and automatic commands governing our bodily functions. This complexity arises partly from large-scale structural variations in the genome, evolutionary processes to increase brain size, function, and cognition. Not surprisingly given recent technical advances, low-grade gliomas (LGGs), which arise from the glia (the most abundant cell type in the brain), have undergone a recent revolution in their classification and therapy, especially in the pediatric setting. Next-generation sequencing has uncovered previously unappreciated diverse LGG entities, unraveling genetic subgroups and multiple molecular alterations and altered pathways, including many amenable to therapeutic targeting. In this article we review these novel entities, in which oncogenic processes show striking age-related neuroanatomical specificity (highlighting their close interplay with development); the opportunities they provide for targeted therapies, some of which are already practiced at the bedside; and the challenges of implementing molecular pathology in the clinic.
Identifiants
pubmed: 31794268
doi: 10.1146/annurev-genet-120417-031642
doi:
Substances chimiques
IDH2 protein, human
EC 1.1.1.41
Isocitrate Dehydrogenase
EC 1.1.1.41
IDH1 protein, human
EC 1.1.1.42.
FGFR1 protein, human
EC 2.7.10.1
Receptor, Fibroblast Growth Factor, Type 1
EC 2.7.10.1
raf Kinases
EC 2.7.11.1
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
483-503Subventions
Organisme : NCI NIH HHS
ID : P01 CA196539
Pays : United States
Organisme : CIHR
ID : MOP-286756
Pays : Canada
Organisme : CIHR
ID : FDN-154307
Pays : Canada