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Molecular imaging of gene therapy for cancer.

机译:癌症基因治疗的分子成像。

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Gene therapy of cancer has been one of the most exciting and elusive areas of scientific and clinical research in the past decade. One of the most critical issues for ensuring success of this therapy is the development of technology for noninvasive monitoring of the location, magnitude and duration of vector-mediated gene expression, as well as the distribution and targeting of vector particles in vivo. In recent years many advances have been made in high-resolution, in vivo imaging methods, including: radionuclide imaging, such as positron emission tomography (PET) and single photon emission tomography (SPECT), magnetic resonance (MR) imaging and spectroscopy, bioluminescence imaging and various fluorescence imaging techniques, including fluorescence-mediated tomography (FMT) and near-infrared fluorescence (NIRF) reflectance imaging. A variety of factors determine the choice of specific imaging system, some of them are the imaging requirements (single or repeated), intended use (animal or human) and spatial requirements (organs versus cellular resolution and depth). This review provides descriptions of modalities applicable to imaging different parameters of vector-mediated gene expression in tumors and stem cell tracking in vivo.
机译:在过去的十年中,癌症的基因治疗一直是科学研究和临床研究中最令人兴奋和难以捉摸的领域之一。确保这种疗法成功的最关键问题之一是开发用于对载体介导的基因表达的位置,大小和持续时间以及体内载体颗粒的分布和靶向进行无创监测的技术。近年来,高分辨率的体内成像方法取得了许多进展,包括:放射性核素成像,例如正电子发射断层扫描(PET)和单光子发射断层扫描(SPECT),磁共振(MR)成像和光谱法,生物发光成像和各种荧光成像技术,包括荧光介导的层析成像(FMT)和近红外荧光(NIRF)反射率成像。各种因素决定了特定成像系统的选择,其中一些因素是成像要求(单次或重复),预期用途(动物或人)和空间要求(器官与细胞分辨率和深度之比)。这篇综述提供了适用于对肿瘤中载体介导的基因表达的不同参数进行成像以及体内干细胞追踪的模式描述。

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