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Engineering Three-Dimensional Tumor Models to Study Glioma Cancer Stem Cells and Tumor Microenvironment

机译:工程三维肿瘤模型研究胶质瘤癌症干细胞和肿瘤微环境

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摘要

Glioblastoma (GBM) is the most common and devastating primary brain tumor, leading to a uniform fatality after diagnosis. A major difficulty in eradicating GBM is the presence of microscopic residual infiltrating disease remaining after multimodality treatment. Glioma cancer stem cells (CSCs) have been pinpointed as the treatment-resistant tumor component that seeds ultimate tumor progression. Despite the key role of CSCs, the ideal preclinical model to study the genetic and epigenetic landmarks driving their malignant behavior while simulating an accurate interaction with the tumor microenvironment (TME) is still missing. The introduction of three-dimensional (3D) tumor platforms, such as organoids and 3D bioprinting, has allowed for a better representation of the pathophysiologic interactions between glioma CSCs and the TME. Thus, these technologies have enabled a more detailed study of glioma biology, tumor angiogenesis, treatment resistance, and even performing high-throughput screening assays of drug susceptibility. First, we will review the foundation of glioma biology and biomechanics of the TME, and then the most up-to-date insights about the applicability of these new tools in malignant glioma research.
机译:胶质母细胞瘤(GBM)是最常见和最常放的原发性脑肿瘤,导致诊断后均匀的死亡。消除GBM的主要困难是多层阶段治疗后剩余微观残留渗透疾病的主要困难。胶质瘤癌症干细胞(CSCs)已被精确地作为种子抗性肿瘤进展的治疗抗肿瘤成分。尽管CSCS的关键作用,但研究遗传和表观遗传地标在模拟与肿瘤微环境(TME)的准确相互作用的同时驾驶恶性行为的理想临床前模型仍然缺失。三维(3D)肿瘤平台(例如有机体和3D生物印刷)的引入已经允许更好地表示胶质瘤CSC和TME之间的病理物理学相互作用。因此,这些技术使得更详细地研究了胶质瘤生物学,肿瘤血管生成,治疗抗性,甚至进行了药物易感性的高通量筛选测定。首先,我们将审查TME的胶质瘤生物学和生物力学的基础,然后是关于这些新工具在恶性胶质瘤研究中的适用性最新的见解。

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