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A Comparative Study of Primary and Recurrent Human Glioblastoma Multiforme Using the Small Animal Imaging and Molecular Expressive Profiles

机译:小动物成像和分子表达谱对原发性和复发性人胶质母细胞瘤形态的比较研究

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Purpose: Glioblastoma multiforme (GBM) is the most malignant brain tumor with the characteristics of highly infiltrative growth and recurrent rate. In this study, we used animal imaging and molecular expressive profiles to investigate the characteristics of the primary tumor (GBM-3) cells and recurrent tumor (S1R1) cells from different GBM patients. Procedures: Bioluminescent imaging and 3T magnetic resonance imaging (MRI) were used for assessing the orthotopical tumor development of GBM cells harboring a polycistronic reporter gene system. Western blot analysis and quantitative polymerase chain reaction were used to compare the molecular expressive profiles of two types of GBM cells. Results: S1R1 cells exhibited apparent invasive ability compared to GBM-3 cells using in vitro invasion assay. In vivo bioluminescent imaging showed that intracranial tumors are formed by both types of GBM cells, but the bioluminescent signal was also detected in the lumbar region at late-stage tumor formed by S1R1 cells. The MRI showed that intracranial tumors formed by S1R1 cells were highly infiltrative compared to that formed by GBM-3 cells. Additionally, these two GBM types expressed different patterns of molecules associated with tumor development. Moreover, the suppressive effects of interleukine-23 (IL-23) on xenograft tumors formed by both GBM types were detected using bioluminescent imaging. Conclusion: The current data suggest that the in vivo growth behaviors and therapeutic responses of the primary and recurrent human GBMs were comparable using the reporter gene imaging, and different molecular expressive profiles exist between these two GBM types.
机译:目的:多形性胶质母细胞瘤(GBM)是最恶性的脑肿瘤,具有高度浸润性生长和复发率的特征。在这项研究中,我们使用动物成像和分子表达谱研究了来自不同GBM患者的原发性肿瘤(GBM-3)细胞和复发性肿瘤(S1R1)细胞的特征。程序:使用生物发光成像和3T磁共振成像(MRI)评估具有多顺反子报告基因系统的GBM细胞的原位肿瘤发展。 Western blot分析和定量聚合酶链反应用于比较两种类型的GBM细胞的分子表达谱。结果:使用体外侵袭试验,与GBM-3细胞相比,S1R1细胞表现出明显的侵袭能力。体内生物发光成像显示两种类型的GBM细胞均形成颅内肿瘤,但在S1R1细胞形成的晚期肿瘤的腰椎区域也检测到生物发光信号。 MRI显示,与GBM-3细胞相比,S1R1细胞形成的颅内肿瘤具有较高的浸润性。另外,这两种GBM类型表达与肿瘤发展相关的分子的不同模式。此外,使用生物发光成像检测了白细胞介素23(IL-23)对两种GBM类型形成的异种移植肿瘤的抑制作用。结论:目前的数据表明,使用报告基因成像,原发性和复发性人GBM的体内生长行为和治疗反应具有可比性,并且这两种GBM类型之间存在不同的分子表达谱。

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