Abstract
Poly(ADP-ribose) polymerase (PARP) is involved in repair of DNA breaks and is over-expressed in a wide variety of tumors, making PARP an attractive biomarker for positron emission tomography (PET) and single photon emission computed tomography imaging. Consequently, over the past decade, there has been a drive to develop nuclear imaging agents targeting PARP. Here, we report the discovery of a PET tracer that is based on the potent PARP inhibitor olaparib (1). Our lead PET tracer candidate, [ 18 F]20, was synthesized and evaluated as a potential PARP PET radiotracer in mice bearing subcutaneous glioblastoma xenografts using ex vivo biodistribution and PET-magnetic resonance imaging techniques. Results showed that [ 18 F]20 could be produced in a good radioactivity yield and exhibited specific PARP binding allowing visualization of tumors over-expressing PARP. [ 18 F]20 is therefore a potential candidate radiotracer for in vivo PARP PET imaging.
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CITATION STYLE
Zmuda, F., Blair, A., Liuzzi, M. C., Malviya, G., Chalmers, A. J., Lewis, D., … Pimlott, S. L. (2018). An 18 F-Labeled Poly(ADP-ribose) Polymerase Positron Emission Tomography Imaging Agent. Journal of Medicinal Chemistry, 61(9), 4103–4114. https://doi.org/10.1021/acs.jmedchem.8b00138
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