Kim Hyun Jung, Park Jung Won, Lee Jeong Ho
Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, South Korea.
SoVarGen, Inc., Daejeon, South Korea.
Front Oncol. 2021 Jan 21;10:615400. doi: 10.3389/fonc.2020.615400. eCollection 2020.
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.
胶质母细胞瘤(GBM)是一种侵袭性原发性脑癌,是成人中枢神经系统中最常见的癌症。然而,无法确定其细胞起源一直是阻碍进一步了解GBM的本质和发病机制以及新型治疗靶点开发的一个基本问题。研究人员推测,GBM源于神经干细胞(NSCs)和神经胶质前体细胞中体细胞突变的积累,这些突变赋予了选择性生长优势,导致不受控制的增殖。在这篇综述中,我们概述了关于异柠檬酸脱氢酶(IDH)野生型和IDH突变型GBM发病机制的基因组学观点,以及各种GBM动物模型提出的携带GBM驱动突变的细胞起源。此外,我们还讨论了在IDH野生型或IDH突变型GBM中观察到的不同神经发育程序。对GBM的细胞起源和谱系层次的进一步研究将有助于理解GBM的演变,并有助于开发治疗GBM癌细胞的有效靶点。