Suppr超能文献

靶向去甲肾上腺素转运体的癌症诊疗新技术——新视野

Norepinephrine Transporter-Targeted Cancer Theranostics-New Horizons.

作者信息

Higuchi Takahiro, Klimek Konrad, Groener Daniel, Chen Xinyu, Werner Rudolf A

机构信息

Clinic for Radiology and Nuclear Medicine, Department of Nuclear Medicine, Goethe University Frankfurt, University Hospital, Frankfurt, Germany.

Nuclear Medicine, Faculty of Medicine, University of Augsburg, Augsburg, Germany.

出版信息

Clin Nucl Med. 2025 Jan 1;50(1):44-51. doi: 10.1097/RLU.0000000000005567. Epub 2024 Nov 19.

Abstract

In the evolving landscape of precision oncology, this review delineates the role of radiopharmaceuticals targeting the norepinephrine transporter (NET), with a particular focus on the current clinical application of 123 I-MIBG diagnostic imaging and 131 I-MIBG therapeutics, in particular for pheochromocytoma, neuroblastoma, or paraganglioma. We will also highlight recently introduced 18 F-labeled NET targeting imaging radiotracers, which would offer unparalleled resolution, enhanced tumor localization, and staging properties. Complementing these novel second-generation PET agents in a theranostic approach, astatine-211 meta-astatobenzylguanidine ( 211 At-MABG) would leverage the advantages of alpha-particles to selectively target and eradicate NET-expressing tumor cells with minimal off-target effects.

摘要

在精准肿瘤学不断发展的背景下,本综述阐述了靶向去甲肾上腺素转运体(NET)的放射性药物的作用,特别关注123I-MIBG诊断成像和131I-MIBG治疗的当前临床应用,尤其是针对嗜铬细胞瘤、神经母细胞瘤或副神经节瘤。我们还将重点介绍最近推出的靶向NET的18F标记成像放射性示踪剂,其具有无与伦比的分辨率、增强的肿瘤定位和分期特性。作为这些新型第二代PET药物在治疗诊断方法中的补充,砹-211间位-砹苄基胍(211At-MABG)将利用α粒子的优势,以最小的脱靶效应选择性地靶向并根除表达NET的肿瘤细胞。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验