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低级别胶质瘤的临床前模型

Preclinical Models of Low-Grade Gliomas.

作者信息

Dasgupta Pushan, Balasubramanyian Veerakumar, de Groot John F, Majd Nazanin K

机构信息

Department of Neurology, Dell Medical School, University of Texas at Austin, Austin, TX 78712, USA.

Department of Neuro-Oncology, UT MD Anderson Cancer Center, Houston, TX 77030, USA.

出版信息

Cancers (Basel). 2023 Jan 18;15(3):596. doi: 10.3390/cancers15030596.

Abstract

Diffuse infiltrating low-grade glioma (LGG) is classified as WHO grade 2 astrocytoma with isocitrate dehydrogenase (IDH) mutation and oligodendroglioma with IDH1 mutation and 1p/19q codeletion. Despite their better prognosis compared with glioblastoma, LGGs invariably recur, leading to disability and premature death. There is an unmet need to discover new therapeutics for LGG, which necessitates preclinical models that closely resemble the human disease. Basic scientific efforts in the field of neuro-oncology are mostly focused on high-grade glioma, due to the ease of maintaining rapidly growing cell cultures and highly reproducible murine tumors. Development of preclinical models of LGG, on the other hand, has been difficult due to the slow-growing nature of these tumors as well as challenges involved in recapitulating the widespread genomic and epigenomic effects of IDH mutation. The most recent WHO classification of CNS tumors emphasizes the importance of the role of IDH mutation in the classification of gliomas, yet there are relatively few IDH-mutant preclinical models available. Here, we review the in vitro and in vivo preclinical models of LGG and discuss the mechanistic challenges involved in generating such models and potential strategies to overcome these hurdles.

摘要

弥漫性浸润性低级别胶质瘤(LGG)被分类为具有异柠檬酸脱氢酶(IDH)突变的世界卫生组织(WHO)2级星形细胞瘤以及具有IDH1突变和1p/19q共缺失的少突胶质细胞瘤。尽管与胶质母细胞瘤相比,LGG的预后较好,但它们总是会复发,导致残疾和过早死亡。对于LGG,发现新的治疗方法的需求尚未得到满足,这就需要与人类疾病高度相似的临床前模型。由于易于维持快速生长的细胞培养物和高度可重复的小鼠肿瘤,神经肿瘤学领域的基础科学研究大多集中在高级别胶质瘤上。另一方面,由于这些肿瘤生长缓慢以及在重现IDH突变的广泛基因组和表观基因组效应方面存在挑战,LGG临床前模型的开发一直很困难。世界卫生组织最新的中枢神经系统肿瘤分类强调了IDH突变在胶质瘤分类中的重要作用,但可用的IDH突变临床前模型相对较少。在这里,我们回顾了LGG的体外和体内临床前模型,并讨论了生成此类模型所涉及的机制挑战以及克服这些障碍的潜在策略。

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