Development of [(18)F]DASA-10 for enhanced imaging of pyruvate kinase M2

开发 [(18)F]DASA-10 用于增强丙酮酸激酶 M2 的成像

阅读:1

Abstract

PURPOSE: The aim of this study was to develop a positron emission tomography (PET) radiotracer for measuring pyruvate kinase M2 (PKM2) with improved physicochemical and pharmacokinetic properties compared to [(18)F]DASA-23. EXPERIMENTAL DESIGN: First, we synthesized [(18)F]DASA-10 and tested its uptake and retention compared to [(18)F]DASA-23 in human and mouse glioma cell lines. We then confirmed the specificity of [(18)F]DASA-10 by transiently modulating the expression of PKM2 in DU145 and HeLa cells. Next, we determined [(18)F]DASA-10 pharmacokinetics in healthy nude mice using PET imaging and subsequently assessed the ability of [(18)F]DASA-10 versus [(18)F]DASA-23 to enable in vivo detection of intracranial gliomas in syngeneic C6 rat models of glioma. RESULTS: [(18)F]DASA-10 demonstrated excellent cellular uptake and retention with values significantly higher than [(18)F]DASA-23 in all cell lines and timepoints investigated. [(18)F]DASA-10 showed a 73 % and 65 % reduced uptake respectively in DU145 and HeLa cells treated with PKM2 siRNA as compared to control siRNA treated cells. [(18)F]DASA-10 showed favorable biodistribution and pharmacokinetic properties and a significantly improved tumor-to-brain ratio in rat C6 glioma models relative to [(18)F]DASA-23 (3.2 ± 0.8 versus 1.6 ± 0.3, p = 0.01). CONCLUSION: [(18)F]DASA-10 is a new PET radiotracer for molecular imaging of PKM2 with potential to overcome the prior limitations observed with [(18)F]DASA-23. [(18)F]DASA-10 shows promise for clinical translation to enable imaging of brain malignancies owing to its low background signal in the healthy brain.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。