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从实验室到临床:白蛋白结合剂改善癌症放射性配体疗法。

Bench to Bedside: Albumin Binders for Improved Cancer Radioligand Therapies.

机构信息

Laboratory of Molecular Imaging and Nanomedicine (LOMIN), National Institute of Biomedical Imaging and Bioengineering (NIBIB) , National Institutes of Health (NIH) , Bethesda , Maryland 20892 , United States.

Department of Molecular Oncology , BC Cancer , Vancouver , British Columbia V5Z 1L3 , Canada.

出版信息

Bioconjug Chem. 2019 Mar 20;30(3):487-502. doi: 10.1021/acs.bioconjchem.8b00919. Epub 2019 Jan 23.

Abstract

Radioligand therapy (RLT) relies on the use of pharmacophores to selectively deliver ionization energy to cancers to exert its tumoricidal effects. Cancer cells that are not directly targeted by a radioconjugate remain susceptible to RLT because of the crossfire effect. This is significant given the inter- and intra-heterogeneity of tumors. In recent years, reversible albumin binders have been used as simple "add-ons" for radiopharmaceuticals to modify pharmacokinetics and to enhance therapeutic efficacy. In this Review, we discuss recent advances in albumin binder platforms used in RLT, with an emphasis on 4-( p-iodophenyl)butyric acid and Evans blue derivatives. We focus on four biological systems pertinent to oncology that utilize this class of compounds: folate receptor, integrin αvβ3, somatostatin receptor, and prostate-specific membrane antigen. Finally, we offer our perspectives on albumin binders for RLT, highlighting future areas of research that will help propel the technology further for clinical use.

摘要

放射性配体治疗 (RLT) 依赖于药理学基团的使用,以选择性地将电离能输送到癌症中,从而发挥其杀肿瘤作用。由于交火效应,未被放射性缀合物直接靶向的癌细胞仍然容易受到 RLT 的影响。考虑到肿瘤的异质性和内在异质性,这一点非常重要。近年来,可逆的白蛋白结合物已被用作放射性药物的简单“附加物”,以改变药代动力学并增强治疗效果。在这篇综述中,我们讨论了 RLT 中使用的白蛋白结合物平台的最新进展,重点介绍了 4-(对碘苯基)丁酸和 Evans 蓝衍生物。我们关注了四个与肿瘤学相关的生物学系统,这些系统利用了这一类化合物:叶酸受体、整合素 αvβ3、生长抑素受体和前列腺特异性膜抗原。最后,我们对 RLT 的白蛋白结合物提出了看法,强调了有助于推动该技术进一步临床应用的未来研究领域。

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