| Literature DB >> 33552990 |
Hyun Jung Kim1, Jung Won Park1, Jeong Ho Lee1,2.
Abstract
An aggressive primary brain cancer, glioblastoma (GBM) is the most common cancer of the central nervous system in adults. However, an inability to identify its cell-of-origin has been a fundamental issue hindering further understanding of the nature and pathogenesis of GBM, as well as the development of novel therapeutic targets. Researchers have hypothesized that GBM arises from an accumulation of somatic mutations in neural stem cells (NSCs) and glial precursor cells that confer selective growth advantages, resulting in uncontrolled proliferation. In this review, we outline genomic perspectives on IDH-wildtype and IDH-mutant GBMs pathogenesis and the cell-of-origin harboring GBM driver mutations proposed by various GBM animal models. Additionally, we discuss the distinct neurodevelopmental programs observed in either IDH-wildtype or IDH-mutant GBMs. Further research into the cellular origin and lineage hierarchy of GBM will help with understanding the evolution of GBMs and with developing effective targets for treating GBM cancer cells.Entities:
Keywords: genetically engineered mouse model; glioblastoma; neural stem cells; somatic mutation; subventricular zone
Year: 2021 PMID: 33552990 PMCID: PMC7859479 DOI: 10.3389/fonc.2020.615400
Source DB: PubMed Journal: Front Oncol ISSN: 2234-943X Impact factor: 6.244