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Glioblastoma models driven by different mutations converge to the proneural subtype

机译:由不同突变驱动的胶质母细胞瘤模型会聚到散装亚型

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摘要

The need of reliable syngeneic animal models for gliomas has been addressed in the last decades by reproducing genetic alterations typical of human glioblastoma in the mouse. Since different alterations underlie different molecular glioblastoma subtypes it is commonly expected that tumors induced by specific alterations represent models of the corresponding subtypes. We tested this assumption by a multilevel analysis ranging from a detailed histopathological analysis to a genome-wide expression profiling by microarray and RNA-seq on gliomas induced by two distinct molecular alterations: the overstimulation of the PDGF- and the EGF- pathways. These alterations are landmarks of proneural and classical glioblastoma subtypes respectively. However, our results consistently showed a strong similarity between the two glioma models. The expression profiles of both models converged toward a signature typical of oligodendrocyte progenitor cells, regardless the wide differentiative potential of the cell of origin. A classification based on similarity with human gliomas profiles revealed that both models belong to the proneural subtype.
机译:通过在小鼠中典型的人胶质母细胞瘤典型的遗传改变来解决过去几十年来解决了Gliomas的可靠同工动物模型的需求。由于不同的改变利于不同的分子胶质母细胞瘤亚型,通常预期由特定改变诱导的肿瘤代表相应亚型的模型。我们通过多级分析测试了这种假设,该假设范围从详细的组织病理学分析到通过微阵列和RNA-SEQ对由两个不同分子改变引起的胶质瘤的基因组表达分析:PDGF和EGF-途径的过度刺激。这些改变分别是散装和古典胶质母细胞瘤亚型的标志性。但是,我们的结果一直在两种胶质瘤模型之间表现出强烈的相似性。两种模型的表达轮廓朝向统一的少压细胞祖细胞细胞统一,无论原产小细胞的宽差潜力如何。基于与人胶质瘤曲线相似性的分类显示,两种模型属于散装亚型。

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