首页> 美国卫生研究院文献>Translational Oncology >In Vivo Bioluminescent Imaging of Irradiated Orthotopic Pancreatic Cancer Xenografts in Nonobese Diabetic-Severe Combined Immunodeficient Mice: A Novel Method for Targeting and Assaying Efficacy of Ionizing Radiation
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In Vivo Bioluminescent Imaging of Irradiated Orthotopic Pancreatic Cancer Xenografts in Nonobese Diabetic-Severe Combined Immunodeficient Mice: A Novel Method for Targeting and Assaying Efficacy of Ionizing Radiation

机译:在非肥胖糖尿病-严重合并免疫缺陷小鼠中辐射原位胰腺癌异种移植物的体内生物发光成像:靶向和测定电离辐射功效的新方法

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摘要

Adenocarcinoma of the pancreas is a lethal malignancy, and better models to study tumor behavior in vivo are needed for the development ofmore effective therapeutics. Ionizing radiation is a treatment modality that is commonly used in the clinical setting, in particular, for locally confined disease; however, good model systems to study the effect of ionizing radiation in orthotopic tumors have not been established. In an attempt to create clinically relevant models for studying treatments directed against pancreatic cancer, we have defined a methodology to measure the effect of varying doses of radiation in established human pancreatic cancer orthotopic xenografts using two different pancreatic cancer cell lines (Panc-1 and BXPC3) infected with a lentiviral vector expressing CMV promoter-driven luciferase to allow bioluminescence imaging of live animals in real time. Quantifiable photon emission from luciferase signaling in vivo correlated well with actual tumor growth. Bioluminescence imaging of the established pancreatic xenografts was used to direct delivery of radiation to the orthotopic tumors and minimize off-target adverse effects. Growth delay was observed with schedules in the range of 7.5 Gy in five fractions to 10 Gy in four fractions, whereas doses 3 Gy or higher produced toxic adverse effects. In conclusion, we describe a model in which the effects of ionizing radiation, alone or in combination with other therapeutics, in orthotopic xenografts, can be studied.
机译:胰腺腺癌是一种致命的恶性肿瘤,为开发更有效的治疗方法,需要更好的模型来研究体内肿瘤行为。电离辐射是一种临床常用的治疗方式,特别是局部局限性疾病。但是,尚未建立研究电离辐射在原位肿瘤中作用的良好模型系统。为了创建临床相关模型来研究针对胰腺癌的治疗方法,我们定义了一种方法,用于使用两种不同的胰腺癌细胞系(Panc-1和BXPC3)测量已建立的人胰腺癌原位异种移植物中不同剂量的放射线的影响)感染了表达CMV启动子驱动的荧光素酶的慢病毒载体,从而可以实时对活体动物进行生物发光成像。体内萤光素酶信号传导的可量化光子发射与实际肿瘤生长密切相关。建立的胰腺异种移植物的生物发光成像可用于将放射线直接传递至原位肿瘤,并最大程度地降低脱靶的不良反应。观察到生长延迟的时间表在五个部分的7.5 Gy至四个部分的10 Gy的范围内,而3 Gy或更高剂量会产生毒性不利影响。总之,我们描述了一个模型,其中可以研究电离辐射单独或与其他疗法组合在原位异种移植物中的作用。

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