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Characterization Of Cells Recovered From The Xenotransplanted Ng97 Human-derived Glioma Cell Line Subcultured In A Long-term In Vitro.

机译:从异体移植的Ng97人源性胶质瘤细胞系中长期体外传代回收的细胞的表征。

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摘要

In order to elucidate tumoral progression and drug resistance, cultured cell lines are valuable tools applied on tumor related assays provided they are well established and characterized. Our laboratory settled the NG97 cell line derived from a human astrocytoma grade III, which started to develop and express important phenotypical characteristics of an astrocytoma grade IV after injection in the flank of nude mice. Astrocytomas are extremely aggressive malignancies of the Central Nervous System (CNS) and account for 46% of all primary malignant brain tumors. Progression to worse prognosis occurs in 85% of the cases possibly due to changes in cell tumor microenvironment and through biological pathways that are still unclear. This work focused on characterizing the NG97 cell line specifically after being recovered from the xenotransplant, who maintained their undifferentiated characteristics along the following 60th passages in vitro. These cells were subcultivated to evaluate the possible contribution of these undifferentiated characteristics to the malignant progression phenotype. These characteristics were the expression of molecules involved in the processes of migration, dedifferentiation and chromosomal instability. Results showed that NG97(ht) had an decrease in doubling time through sub cultivation, which was characterized by a converse modulation between the expression of glial fibrillary acidic protein (GFAP) and vimentin. In addition, beta1 integrins were present in intermediate levels while alpha5 integrins had a high expression profile as well as fibronectin and laminin. Cytogenetic analysis of NG97(ht) revealed several chromosomal abnormalities, 89% of the cells showed to be hyperdiploid and the modal number was assigned to be 63. Several acrocentric chromosomes were visualized and at least 30 figures were attributed to be murine. These findings suggest a possible fusion between the original NG97 cells with stromal murine cells in the xenotransplant. In this study the NG97(ht) cells were characterized to embryonic recovery patterns of intermediate filaments, adhesion molecules expression, chromosomal imbalances and murine chromosomes. In the latter case, these presumably chromosomes were originated as fusions between murine stroma cells and NG97 cell lineage in the xenotransplant. Our results emphasize important queries about astrocytomas tumor progression.
机译:为了阐明肿瘤的进展和耐药性,培养的细胞系是建立在肿瘤相关测定中的有价值的工具,条件是它们已得到很好的建立和表征。我们的实验室解决了源自人类星形细胞瘤III级的NG97细胞系的问题,该细胞系在裸鼠腹侧注射后开始发展并表达了星形细胞瘤IV级的重要表型特征。星形细胞瘤是中枢神经系统(CNS)极具侵略性的恶性肿瘤,占所有原发性恶性脑肿瘤的46%。在85%的病例中可能发生预后恶化,这可能是由于细胞肿瘤微环境的变化以及尚不清楚的生物学途径所致。这项工作着重于表征NG97细胞系,特别是从异种移植物中回收后,其在随后的第60代中保持了未分化的特性。将这些细胞传代培养,以评估这些未分化特征对恶性进展表型的可能贡献。这些特征是参与迁移,去分化和染色体不稳定过程的分子表达。结果表明,NG97(ht)通过亚培养具有倍增时间的减少,其特征在于神经胶质纤维酸性蛋白(GFAP)和波形蛋白之间的逆向调控。此外,beta1整联蛋白以中等水平存在,而alpha5整联蛋白以及纤连蛋白和层粘连蛋白具有高表达谱。 NG97(ht)的细胞遗传学分析显示了几个染色体异常,其中89%的细胞显示为超二倍体,并且模态编号为63。可视化了多个顶心染色体,并且至少有30个数字被归因于鼠。这些发现表明异种移植中原始NG97细胞与基质鼠细胞之间可能融合。在这项研究中,NG97(ht)细胞的特征在于中间细丝的胚胎恢复模式,粘附分子表达,染色体失衡和鼠染色体。在后一种情况下,这些推测的染色体起源于异种移植物中鼠基质细胞与NG97细胞谱系之间的融合。我们的结果强调了有关星形细胞瘤肿瘤进展的重要问题。

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