The detection of human epidermal growth factor receptor type 2 (HER2) expression in malignant tumors provides important information influencing patient management. Radionuclide in vivo imagi'/> Targeting of HER2-Expressing Tumors with a Site-Specifically 99mTc-Labeled Recombinant Affibody Molecule, ZHER2:2395, with C-Terminally Engineered Cysteine
首页> 外文期刊>The Journal of Nuclear Medicine >Targeting of HER2-Expressing Tumors with a Site-Specifically 99mTc-Labeled Recombinant Affibody Molecule, ZHER2:2395, with C-Terminally Engineered Cysteine
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Targeting of HER2-Expressing Tumors with a Site-Specifically 99mTc-Labeled Recombinant Affibody Molecule, ZHER2:2395, with C-Terminally Engineered Cysteine

机译:用带有C末端工程半胱氨酸的特定位点特异性99mTc标签的重组亲和体分子(ZHER2:2395)靶向表达HER2的肿瘤。

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id="p-1">The detection of human epidermal growth factor receptor type 2 (HER2) expression in malignant tumors provides important information influencing patient management. Radionuclide in vivo imaging of HER2 may permit the detection of HER2 in both primary tumors and metastases by a single noninvasive procedure. Small (7 kDa) high-affinity anti-HER2 Affibody molecules may be suitable tracers for SPECT visualization of HER2-expressing tumors. The use of generator-produced 99mTc as a label would facilitate the prompt translation of anti-HER2 Affibody molecules into use in clinics. >Methods: A C-terminal cysteine was introduced into the Affibody molecule ZHER2:342 to enable site-specific labeling with 99mTc. Two recombinant variants, His6-ZHER2:342-Cys (dissociation constant [KD], 29 pM) and ZHER2:2395-Cys, lacking a His tag (KD, 27 pM), were labeled with 99mTc in yields exceeding 90%. The binding specificity and the cellular processing of Affibody molecules were studied in vitro. Biodistribution and ?3-camera imaging studies were performed in mice bearing HER2-expressing xenografts. >Results: 99mTc-His6-ZHER2:342-Cys was capable of targeting HER2-expressing SKOV-3 xenografts in SCID mice, but the liver radioactivity uptake was high. A series of comparative biodistribution experiments indicated that the presence of the His tag caused elevated accumulation in the liver. 99mTc-ZHER2:2395-Cys, not containing a His tag, showed low uptake in the liver and high and specific uptake in HER2-expressing xenografts. Four hours after injection, the radioactivity uptake values (percentage of injected activity per gram of tissue [%IA/g]) were 6.9 ?± 2.5 (mean ?± SD) %IA/g in LS174T xenografts (moderate level of HER2 expression) and 15 ?± 3 %IA/g in SKOV-3 xenografts (high level of HER2 expression). The corresponding tumor-to-blood ratios were 88 ?± 24 and 121 ?± 24, respectively. Both LS174T and SKOV-3 xenografts were clearly visualized with a clinical ?3-camera 1 h after injection of 99mTc-ZHER2:2395-Cys. >Conclusion: The Affibody molecule 99mTc-ZHER2:2395-Cys is a promising tracer for SPECT visualization of HER2-expressing tumors.
机译:id =“ p-1”>在恶性肿瘤中检测人类表皮生长因子2型受体(HER2)的表达可提供影响患者治疗的重要信息。 HER2的放射性核素体内成像可通过单一非侵入性程序检测原发性肿瘤和转移灶中的HER2。小(7 kDa)高亲和力的抗HER2 Affibody分子可能是合适的示踪剂,用于SPECT可视化表达HER2的肿瘤。使用发电机产生的 99m Tc作为标签,将有助于迅速将抗HER2 Affibody分子转化为临床应用。 >方法:将C端半胱氨酸引入Affibody分子Z HER2:342 中,以实现 99m Tc的位点特异性标记。两个重组变体,His 6 -Z HER2:342 -Cys(解离常数[K D ],29 pM)和Z HER2:2395 -Cys,缺少His标签(K D ,27 pM),用 99m Tc标记,收率超过90%。在体外研究了Affibody分子的结合特异性和细胞加工。在带有表达HER2的异种移植物的小鼠中进行了生物分布和β3相机成像研究。 >结果:: 99m Tc-His 6 -Z HER2:342 -Cys能够靶向表达HER2的SKOV在SCID小鼠中有-3异种移植物,但肝脏放射性摄取较高。一系列比较性的生物分布实验表明,His标签的存在导致肝脏中的积累升高。不包含His标签的 99m Tc-Z HER2:2395 -Cys在肝脏中摄取低,而在表达HER2的异种移植物中摄取高且特异性。注射后四小时,LS174T异种移植物中的放射性吸收值(每克组织注射活性的百分比[%IA / g])为6.9±±2.5(平均值±SD)%IA / g(中等水平的HER2表达)在SKOV-3异种移植物中(HER2的高表达水平)为15?±3%IA / g。相应的肿瘤与血液的比率分别为88±±24和121±±24。注射 99m Tc-Z HER2:2395 -Cys 1小时后,用临床β3-照相机清晰观察到了LS174T和SKOV-3异种移植物。 >结论: Affibody分子 99m Tc-Z HER2:2395 -Cys是用于SPECT可视化表达HER2的肿瘤的有希望的示踪剂。

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