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http://dx.doi.org/10.3348/kjr.2010.11.4.449

Visualization of Tumor Angiogenesis Using MR Imaging Contrast Agent Gd-DTPA-anti-VEGF Receptor 2 Antibody Conjugate in a Mouse Tumor Model  

Jun, Hong-Young (Institute for Radiological Imaging Science, Wonkwang University Schoolof Medicine)
Yin, Hong-Hua (Institute for Radiological Imaging Science, Wonkwang University Schoolof Medicine)
Kim, Sun-Hee (Institute for Radiological Imaging Science, Wonkwang University Schoolof Medicine)
Park, Seong-Hoon (Department of Radiology, Wonkwang University School of Medicine)
Kim, Hun-Soo (Department of Pathology, Wonkwang University School of Medicine)
Yoon, Kwon-Ha (Institute for Radiological Imaging Science, Wonkwang University Schoolof Medicine)
Publication Information
Korean Journal of Radiology / v.11, no.4, 2010 , pp. 449-456 More about this Journal
Abstract
Objective: To visualize tumor angiogenesis using the MRI contrast agent, Gd- DTPA-anti-VEGF receptor 2 antibody conjugate, with a 4.7-Tesla MRI instrument in a mouse model. Materials and Methods: We designed a tumor angiogenesis-targeting T1 contrast agent that was prepared by the bioconjugation of gadolinium diethylenetriaminepentaacetic acid (Gd-DTPA) and an anti-vascular endothelial growth factor receptor-2 (VEGFR2) antibody. The specific binding of the agent complex to cells that express VEGFR2 was examined in cultured murine endothelial cells (MS-1 cells) with a 4.7-Tesla magnetic resonance imaging scanner. Angiogenesis-specific T1 enhancement was imaged with the Gd-DTPA-anti-VEGFR2 antibody conjugate using a CT-26 adenocarcinoma tumor model in eight mice. As a control, the use of the Gd-DTPA-anti-rat immunoglobulin G (Gd-DTPA-anti-rat IgG) was imaged with a tumor model in eight mice. Statistical significance was assessed using the Mann-Whitney test. Tumor tissue was examined by immunohistochemical analysis. Results: The Gd-DTPA-anti-VEGFR2 antibody conjugate showed predominant binding to cultured endothelial cells that expressed a high level of VEGFR2. Signal enhancement was approximately three-fold for in vivo T1-weighted MR imaging with the use of the Gd-DTPA-anti-VEGFR2 antibody conjugate as compared with the Gd-DTPA-rat IgG in the mouse tumor model (p < 0.05). VEGFR2 expression in CT-26 tumor vessels was demonstrated using immunohistochemical staining. Conclusion: MR imaging using the Gd-DTPA-anti-VEGFR2 antibody conjugate as a contrast agent is useful in visualizing noninvasively tumor angiogenesis in a murine tumor model.
Keywords
Magnetic resonance (MR) contrast agent; Molecular Imaging; Angiogenesis; Bioconjugation;
Citations & Related Records
Times Cited By KSCI : 2  (Citation Analysis)
Times Cited By Web Of Science : 3  (Related Records In Web of Science)
Times Cited By SCOPUS : 4
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