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多区域采样来源的胶质瘤干细胞中的功能和分子异质性

Functional and Molecular Heterogeneity in Glioma Stem Cells Derived from Multiregional Sampling.

作者信息

Brynjulvsen Marit, Solli Elise, Walewska Maria, Zucknick Manuela, Djirackor Luna, Langmoen Iver A, Mughal Awais Ahmad, Skaga Erlend, Vik-Mo Einar O, Sandberg Cecilie J

机构信息

Vilhelm Magnus Lab, Institute for Surgical Research and Department of Neurosurgery, Oslo University Hospital, Nydalen, P.O. Box 4950, 0424 Oslo, Norway.

Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Blindern, P.O. Box 1112, 0317 Oslo, Norway.

出版信息

Cancers (Basel). 2023 Dec 13;15(24):5826. doi: 10.3390/cancers15245826.

Abstract

Glioblastoma (GBM) is an aggressive and highly heterogeneous primary brain tumor. Glioma stem cells represent a subpopulation of tumor cells with stem cell traits that are presumed to be the cause of tumor relapse. There exists complex tumor heterogeneity in drug sensitivity patterns between glioma stem cell (GSC) cultures derived from different patients. Here, we describe that heterogeneity also exists between GSC cultures derived from multiple biopsies within a single tumor. From biopsies harvested within spatially distinct regions representing the entire tumor mass, we established seven GSC cultures and compared their stem cell properties, mutations, gene expression profiles, and drug sensitivity patterns against 115 different anticancer drugs. The results were compared to 14 GSC cultures derived from other patients. Between the multiregional-derived GSC cultures, we observed only minor differences in their phenotype, proliferative capacity, and global gene expression. Further, they displayed intratumoral heterogeneity in mutational profiles and sensitivity patterns to anticancer drugs. This heterogeneity, however, did not exceed the extensive heterogeneity found between GSC cultures derived from other GBM patients. Our results suggest that the use of GSC cultures from one single focal biopsy may underestimate the overall complexity of the GSC population and display the importance of including GSC cultures reflecting the entire tumor mass in drug screening strategies.

摘要

胶质母细胞瘤(GBM)是一种侵袭性强且高度异质性的原发性脑肿瘤。胶质瘤干细胞代表具有干细胞特征的肿瘤细胞亚群,被认为是肿瘤复发的原因。来自不同患者的胶质瘤干细胞(GSC)培养物在药物敏感性模式方面存在复杂的肿瘤异质性。在此,我们描述了在源自单个肿瘤内多次活检的GSC培养物之间也存在异质性。从代表整个肿瘤块的空间不同区域采集的活检样本中,我们建立了七种GSC培养物,并针对115种不同的抗癌药物比较了它们的干细胞特性、突变、基因表达谱和药物敏感性模式。将结果与来自其他患者的14种GSC培养物进行比较。在多区域来源的GSC培养物之间,我们仅观察到它们在表型、增殖能力和整体基因表达方面存在微小差异。此外,它们在突变谱和对抗癌药物的敏感性模式方面表现出肿瘤内异质性。然而,这种异质性并未超过在源自其他GBM患者的GSC培养物之间发现的广泛异质性。我们的结果表明,使用来自单次局灶活检的GSC培养物可能会低估GSC群体的整体复杂性,并显示出在药物筛选策略中纳入反映整个肿瘤块的GSC培养物的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2b3/10741477/03ca627f4bb7/cancers-15-05826-g002.jpg

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