CLT1-(Gd-DTPA)对小鼠乳腺癌模型肿瘤磁共振分子成像的评价

Pub Date : 2011-01-01
Furong Ye, Eun-Kee Jeong, Denis Parker, Zheng-Rong Lu
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引用次数: 0

摘要

研究了一种肽靶向造影剂CLT1-(Gd-DTPA)在磁共振成像(MRI)中对肿瘤基质中纤维蛋白-纤维连接蛋白复合物的分子成像。在Siemens 3T临床扫描仪上对携带MDA-MB-231人乳腺癌异种移植物的雌性裸鼠进行对比剂评价,临床药物Gd(DTPA-BMA)作为非靶向对照。CLT1-(Gd-DTPA)以0.05 mmol/kg的剂量特异性结合肿瘤组织,在注射后至少60分钟内显著增强肿瘤造影剂。相比之下,一种非靶向造影剂Gd(DTPA-BMA)在注射0.1 mmol/kg剂量后30分钟后迅速从体内清除,肿瘤几乎没有增强。与对照剂相比,CLT1-(Gd-DTPA)在血液和正常组织(包括肝脏和肌肉)中几乎没有非特异性结合,导致正常组织中的非特异性增强。研究表明,CLT1-(Gd-DTPA)可以与肿瘤组织结合,在小鼠乳腺癌模型中导致肿瘤显著增强。这种靶向造影剂有可能用于乳腺癌的磁共振分子成像。
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Evaluation of CLT1-(Gd-DTPA) for Cancer MR Molecular Imaging in a Mouse Breast Cancer Model.

A peptide targeted contrast agent, CLT1-(Gd-DTPA), was investigated for molecular imaging of fibrin-fibronectin complexes in tumor stroma with magnetic resonance imaging (MRI). The contrast agent was evaluated in female nude mice bearing MDA-MB-231 human breast carcinoma xenografts on a Siemens 3T clinical scanner with a clinical agent Gd(DTPA-BMA) as a non-targeted control. CLT1-(Gd-DTPA) specifically bound to tumor tissue and resulted in significant tumor contrast enhancement at a dose of 0.05 mmol/kg for at least 60 minutes after injection. In contrast, a non-targeted contrast agent, Gd(DTPA-BMA), cleared rapidly from the body with little tumor enhancement after 30 minutes post-injection at a dose of 0.1 mmol/kg. CLT1-(Gd-DTPA) had little non-specific binding in blood and normal tissues, including the liver and muscle, resulting in comparable non-specific enhancement in normal tissues as the control agent. The study has shown that CLT1-(Gd-DTPA) can bind to the tumor tissue, resulting in significant tumor enhancement in a mouse breast cancer model. The targeted contrast agent has a potential for MR molecular imaging of breast cancer.

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