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An (18)F-Labeled Poly(ADP-ribose) Polymerase Positron Emission Tomography Imaging Agent

[Image: see text] 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 d...

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Detalles Bibliográficos
Autores principales: Zmuda, Filip, Blair, Adele, Liuzzi, Maria Clara, Malviya, Gaurav, Chalmers, Anthony J., Lewis, David, Sutherland, Andrew, Pimlott, Sally L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6007963/
https://www.ncbi.nlm.nih.gov/pubmed/29630818
http://dx.doi.org/10.1021/acs.jmedchem.8b00138
Descripción
Sumario:[Image: see text] 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.