The Synthesis and Initial Evaluation of MerTK Targeted PET Agents

被引:1
|
作者
Wang, Li [1 ,2 ]
Zhou, Yubai [3 ]
Wu, Xuedan [1 ,2 ]
Ma, Xinrui [1 ,2 ]
Li, Bing [3 ]
Ding, Ransheng [3 ]
Stashko, Michael A. [3 ]
Wu, Zhanhong [1 ,2 ]
Wang, Xiaodong [3 ]
Li, Zibo [1 ,2 ]
机构
[1] Univ North Carolina Chapel Hill, Biomed Res Imaging Ctr, Dept Radiol, Chapel Hill, NC 27514 USA
[2] Univ North Carolina Chapel Hill, UNC Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27514 USA
[3] Univ North Carolina Chapel Hill, Ctr Integrat Chem Biol & Drug Discovery, Div Chem Biol & Med Chem, Eshelman Sch Pharm, Chapel Hill, NC 27599 USA
来源
MOLECULES | 2022年 / 27卷 / 05期
关键词
MerTK; positron emission tomography; fluorine-18; radiolabeling; cancer; TYROSINE KINASE; THERAPEUTIC TARGET; UNC2025;
D O I
10.3390/molecules27051460
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MerTK (Mer tyrosine kinase), a receptor tyrosine kinase, is ectopically or aberrantly expressed in numerous human hematologic and solid malignancies. Although a variety of MerTK targeting therapies are being developed to enhance outcomes for patients with various cancers, the sensitivity of tumors to MerTK suppression may not be uniform due to the heterogeneity of solid tumors and different tumor stages. In this report, we develop a series of radiolabeled agents as potential MerTK PET (positron emission tomography) agents. In our initial in vivo evaluation, [F-18]-MerTK-6 showed prominent uptake rate (4.79 +/- 0.24%ID/g) in B16F10 tumor-bearing mice. The tumor to muscle ratio reached 1.86 and 3.09 at 0.5 and 2 h post-injection, respectively. In summary, [F-18]-MerTK-6 is a promising PET agent for MerTK imaging and is worth further evaluation in future studies.
引用
收藏
页数:11
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