Noninvasive positron emission tomography and fluorescence imaging of CD133+ tumor stem cells

被引:77
作者
Gaedicke, Simone [1 ]
Braun, Friederike [2 ,4 ]
Prasad, Shruthi [1 ,4 ]
Machein, Marcia [3 ]
Firat, Elke [1 ]
Hettich, Michael [1 ,4 ]
Gudihal, Ravindra [5 ]
Zhu, Xuekai [1 ]
Klingner, Kerstin [6 ]
Schueler, Julia [6 ]
Herold-Mende, Christel C. [7 ]
Grosu, Anca-Ligia [1 ,8 ]
Behe, Martin [2 ,9 ]
Weber, Wolfgang [2 ,8 ,10 ]
Maecke, Helmut [2 ,8 ]
Niedermann, Gabriele [1 ,8 ]
机构
[1] Univ Hosp Freiburg, Dept Radiat Oncol, D-79106 Freiburg, Germany
[2] Univ Hosp Freiburg, Dept Nucl Med, D-79106 Freiburg, Germany
[3] Univ Hosp Freiburg, Dept Neurosurg, D-79106 Freiburg, Germany
[4] Univ Freiburg, Fac Biol, D-79104 Freiburg, Germany
[5] Agilent Technol India Pvt Ltd, Bangalore 560048, Karnataka, India
[6] Oncotest, D-79108 Freiburg, Germany
[7] Univ Heidelberg Hosp, Dept Neurosurg, D-69120 Heidelberg, Germany
[8] German Consortium Translat Canc Res, D-69120 Heidelberg, Germany
[9] Paul Scherrer Inst, Univ Zurich Hosp, Swiss Fed Inst Technol, Ctr Radiopharmaceut Sci, CH-5232 Villigen, Switzerland
[10] Mem Sloan Kettering Canc Ctr, Mol Imaging & Therapy Serv, New York, NY 10065 USA
关键词
cancer stem cells; CSCs; glioblastoma; CLINICAL-IMPLICATIONS; HEMATOPOIETIC STEM; CANCER; GLIOBLASTOMA; GROWTH; AC133; POPULATION; EXPRESSION; THERAPY; MARKER;
D O I
10.1073/pnas.1314189111
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A technology that visualizes tumor stem cells with clinically relevant tracers could have a broad impact on cancer diagnosis and treatment. The AC133 epitope of CD133 currently is one of the best-characterized tumor stem cell markers for many intra-and extracranial tumor entities. Here we demonstrate the successful noninvasive detection of AC133(+) tumor stem cells by PET and near-infrared fluorescence molecular tomography in subcutaneous and orthotopic glioma xenografts using antibody-based tracers. Particularly, microPET with Cu-64-NOTA-AC133 mAb yielded high-quality images with outstanding tumor-to-background contrast, clearly delineating subcutaneous tumor stem cell-derived xenografts from surrounding tissues. Intracerebral tumors as small as 2-3 mm also were clearly discernible, and the microPET images reflected the invasive growth pattern of orthotopic cancer stem cell-derived tumors with low density of AC133(+) cells. These data provide a basis for further preclinical and clinical use of the developed tracers for high-sensitivity and high-resolution monitoring of AC133(+) tumor stem cells.
引用
收藏
页码:E692 / E701
页数:10
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