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首页> 外文期刊>Korean journal of radiology: official journal of the Korean Radiological Society >Visualization of tumor angiogenesis using MR imaging contrast agent Gd-DTPA-anti-VEGF receptor 2 antibody conjugate in a mouse tumor model
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Visualization of tumor angiogenesis using MR imaging contrast agent Gd-DTPA-anti-VEGF receptor 2 antibody conjugate in a mouse tumor model

机译:使用MR成像造影剂Gd-DTPA-抗VEGF受体2抗体偶联物在小鼠肿瘤模型中可视化肿瘤血管生成

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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.
机译:目的:使用MRI造影剂Gd-DTPA-抗VEGF受体2抗体结合物和4.7-Tesla MRI仪器在小鼠模型中观察肿瘤血管生成。材料和方法:我们设计了靶向肿瘤血管生成的T1造影剂,该造影剂是通过di二亚乙基三胺五乙酸(Gd-DTPA)和抗血管内皮生长因子受体2(VEGFR2)抗体的生物偶联制备的。用4.7-Tesla磁共振成像扫描仪在培养的鼠内皮细胞(MS-1细胞)中检查了试剂复合物与表达VEGFR2的细胞的特异性结合。使用CT-26腺癌肿瘤模型,在8只小鼠中用Gd-DTPA-抗-VEGFR2抗体偶联物对血管生成特异性T1增强进行了成像。作为对照,使用Gd-DTPA-抗大鼠免疫球蛋白G(Gd-DTPA-抗大鼠IgG)在八只小鼠的肿瘤模型中成像。使用Mann-Whitney检验评估统计学显着性。通过免疫组织化学分析检查肿瘤组织。结果:Gd-DTPA-抗VEGFR2抗体偶联物显示出与培养的内皮细胞的主要结合,内皮细胞表达高水平的VEGFR2。与小鼠肿瘤模型中的Gd-DTPA-rat IgG相比,使用Gd-DTPA-抗-VEGFR2抗体偶联物进行的体内T1加权MR成像的信号增强约为三倍(p <0.05)。使用免疫组织化学染色证实了CT-26肿瘤血管中VEGFR2的表达。结论:使用Gd-DTPA-抗-VEGFR2抗体偶联物作为造影剂的MR成像可用于可视化鼠肿瘤模型中的非侵入性肿瘤血管生成。

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