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放射性标记肽的体外与体内数据的相关性及其在肿瘤靶向中的应用。

Correlation between in vitro and in vivo Data of Radiolabeled Peptide for Tumor Targeting.

机构信息

Department of Radiopharmacy, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran.

Student Research Committee, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran.

出版信息

Mini Rev Med Chem. 2019;19(12):950-960. doi: 10.2174/1389557519666190304120011.

Abstract

Tumor-targeting peptides have been generally developed for the overexpression of tumor specific receptors in cancer cells. The use of specific radiolabeled peptide allows tumor visualization by single photon emission computed tomography (SPECT) and positron emission tomography (PET) tools. The high affinity and specific binding of radiolabeled peptide are focusing on tumoral receptors. The character of the peptide itself, in particular, its complex molecular structure and behaviors influence on its specific interaction with receptors which are overexpressed in tumor. This review summarizes various strategies which are applied for the expansion of radiolabeled peptides for tumor targeting based on in vitro and in vivo specific tumor data and then their data were compared to find any correlation between these experiments. With a careful look at previous studies, it can be found that in vitro unblock-block ratio was unable to correlate the tumor to muscle ratio and the success of radiolabeled peptide for in vivo tumor targeting. The introduction of modifiers' approaches, nature of peptides, and type of chelators and co-ligands have mixed effect on the in vitro and in vivo specificity of radiolabeled peptides.

摘要

肿瘤靶向肽通常是为了在癌细胞中过表达肿瘤特异性受体而开发的。使用特定的放射性标记肽可以通过单光子发射计算机断层扫描 (SPECT) 和正电子发射断层扫描 (PET) 工具来可视化肿瘤。放射性标记肽的高亲和力和特异性结合集中在肿瘤受体上。肽本身的特性,特别是其复杂的分子结构和行为,影响其与肿瘤中过表达的受体的特异性相互作用。本综述总结了基于体外和体内特定肿瘤数据应用于扩展放射性标记肽以用于肿瘤靶向的各种策略,然后比较它们的数据以发现这些实验之间的任何相关性。仔细研究以前的研究,可以发现体外非阻断-阻断比无法与肿瘤与肌肉比以及放射性标记肽在体内肿瘤靶向中的成功相关联。修饰剂方法、肽的性质以及螯合剂和共配体的类型对放射性标记肽的体外和体内特异性都有混合影响。

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