PARPi-FL - a Fluorescent PARP1 Inhibitor for Glioblastoma Imaging

被引:53
作者
Irwin, Christopher P. [1 ]
Portorreal, Yasiri [1 ]
Brand, Christian [1 ]
Zhang, Yachao [1 ]
Desai, Pooja [1 ]
Salinas, Beatriz [1 ]
Weber, Wolfgang A. [2 ,3 ]
Reiner, Thomas [1 ,4 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Radiol, Radiochem & Imaging Sci Serv, New York, NY 10065 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Radiol, Mol Imaging & Therapy Serv, New York, NY 10065 USA
[3] Mem Sloan Kettering Canc Ctr, Mol Pharmacol & Chem Program, New York, NY 10065 USA
[4] Mem Sloan Kettering Canc Ctr, Ctr Mol Imaging & Nanotechnol, New York, NY 10065 USA
来源
NEOPLASIA | 2014年 / 16卷 / 05期
关键词
RESECTION; SURVIVAL; GLIOMA; EXTENT; EXPRESSION; OLAPARIB; GUIDANCE; SURGERY;
D O I
10.1016/j.neo.2014.05.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
New intravital optical imaging technologies have revolutionized our understanding of mammalian biology and continue to evolve rapidly. However, there are only a limited number of imaging probes available to date. In this study, we investigated in mouse models of glioblastoma whether a fluorescent small molecule inhibitor of the DNA repair enzyme PARP1, PARPi-FL, can be used as an imaging agent to detect glioblastomas in vivo. We demonstrated that PARPi-FL has appropriate biophysical properties, low toxicity at concentrations used for imaging, high stability in vivo, and accumulates selectively in glioblastomas due to high PARP1 expression. Importantly, subcutaneous and orthotopic glioblastoma xenografts were imaged with high contrast clearly defining tumor tissue from normal surrounding tissue. This research represents a step toward exploring and developing PARPi-FL as an optical intraoperative imaging agent for PARP1 in the clinic.
引用
收藏
页码:432 / 440
页数:9
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