A Protocol for the Generation of Treatment-naïve Biopsy-derived Diffuse Intrinsic Pontine Glioma and Diffuse Midline Glioma Models.

Matt C Biery, Alyssa Noll, Carrie Myers, Shelli M Morris, Conrad A Winter, Fiona Pakiam, Bonnie L Cole, Samuel R Browd, James M Olson, Nicholas A Vitanza
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Abstract

Diffuse intrinsic pontine glioma (DIPG) is a universally fatal tumor of the brainstem, most commonly affecting young children. Due to its location, surgical resection is not achievable, but consideration of a biopsy has become standard practice at children's hospitals with the appropriate neurosurgical expertise. While the decision to obtain a biopsy should be directed by the presence of atypical radiographic features that call the diagnosis of DIPG into question or the requirement of biopsy tissue for clinical trial enrollment, once this precious tissue is available its use for research should be considered. The majority of DIPG and diffuse midline glioma, H3 K27M-mutant (DMG) models are autopsy-derived or genetically-engineered, each of which has limitations for translational studies, so the use of biopsy tissue for laboratory model development provides an opportunity to create unique model systems. Here, we present a detailed laboratory protocol for the generation of treatment-naïve biopsy-derived DIPG/DMG models.

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生成未经治疗的活检衍生弥漫性内侧脑桥胶质瘤和弥漫性中线胶质瘤模型的方案。
弥漫性桥脑胶质瘤(DIPG)是一种普遍致命的脑干肿瘤,最常见于幼儿。由于其位置特殊,无法进行手术切除,但在具备相应神经外科专业知识的儿童医院,考虑进行活检已成为标准做法。在决定是否进行活检时,应考虑是否存在非典型放射学特征,从而对 DIPG 的诊断提出质疑,或者是否需要活检组织用于临床试验,一旦获得了这些珍贵的组织,就应考虑将其用于研究。大多数DIPG和弥漫中线胶质瘤、H3 K27M突变体(DMG)模型都来自尸检或基因工程,这两种模型在转化研究中都有局限性,因此使用活检组织进行实验室模型开发为创建独特的模型系统提供了机会。在此,我们介绍了一种生成未经治疗的活检衍生 DIPG/DMG 模型的详细实验室方案。
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