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在人小细胞肺癌裸鼠原位模型中使用生物发光成像和计算机断层扫描监测肿瘤进展。

Monitoring of tumour progression using bioluminescence imaging and computed tomography scanning in a nude mouse orthotopic model of human small cell lung cancer.

机构信息

Inserm U618, Université François Rabelais, IFR 135, F-37032 Tours, France.

出版信息

Lung Cancer. 2012 Jul;77(1):70-6. doi: 10.1016/j.lungcan.2012.01.009. Epub 2012 Feb 8.

Abstract

Human small cell lung carcinoma (SCLC) is the most aggressive type of lung cancer but no clinically relevant animal model has been developed to date. Such a model would be valuable to study the molecular aspects of tumour progression and to test the effectiveness of new treatment agents. We generated a reproducible and reliable nude mouse orthotopic model of human SCLC with NCI-H209 tumour cells genetically modified to express firefly luciferase. Cells were analysed for long-term stability of bioluminescence and a clone was passaged twice subcutaneously to enhance tumorigenicity. Cells resuspended in Matrigel and/or EDTA RPMI medium containing a (99m)Tc-labelled tin colloid used as tracer were implanted intrabronchially with a catheter inserted into the trachea and positioned in the main bronchus using X-ray-guided imaging. Deposition of cells into the lung was then assessed by scintigraphy. The growth of the primary tumour was sensitively and non-invasively followed by bioluminescence imaging that allowed real-time monitoring of tumour progression in the same animals over a 2-12-week period. Additional 3D bioluminescence imaging and computed tomography scanning were used to document tumour location and measurements that were confirmed by histological analyses. In conclusion, this original nude mouse orthotopic model resembles various stages of human small cell lung cancer, and therefore could be used to evaluate new treatment strategies.

摘要

人小细胞肺癌(SCLC)是最具侵袭性的肺癌类型,但迄今为止尚未开发出具有临床相关性的动物模型。这样的模型对于研究肿瘤进展的分子方面以及测试新治疗药物的有效性将非常有价值。我们使用 NCI-H209 肿瘤细胞生成了一种可重复且可靠的裸鼠原位人 SCLC 模型,这些细胞经过基因修饰后表达萤火虫荧光素酶。对细胞进行了长期生物发光稳定性分析,并通过皮下传代两次来增强其致瘤性。将细胞悬浮在 Matrigel 和/或 EDTA RPMI 培养基中,其中含有用作示踪剂的 (99m)Tc 标记锡胶体,通过插入气管的导管将其支气管内植入,然后使用 X 射线引导成像将其定位在主支气管中。然后通过闪烁扫描术评估细胞在肺部的沉积情况。通过生物发光成像来敏感、无创地监测原发性肿瘤的生长,该成像可以在同一动物中实时监测肿瘤在 2-12 周期间的进展情况。还使用了额外的 3D 生物发光成像和计算机断层扫描来记录肿瘤的位置和测量值,并通过组织学分析进行了确认。总之,这种原始的裸鼠原位模型类似于人小细胞肺癌的各个阶段,因此可用于评估新的治疗策略。

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