| Literature DB >> 26212031 |
Sangeeta Ray Banerjee1, Ethel J Ngen2, Matthew W Rotz3, Samata Kakkad2, Ala Lisok2, Richard Pracitto2, Mrudula Pullambhatla2, Zhengping Chen2, Tariq Shah2, Dmitri Artemov2, Thomas J Meade3, Zaver M Bhujwalla2, Martin G Pomper2.
Abstract
Magnetic resonance (MR) imaging is advantageous because it concurrently provides anatomic, functional, and molecular information. MR molecular imaging can combine the high spatial resolution of this established clinical modality with molecular profiling in vivo. However, as a result of the intrinsically low sensitivity of MR imaging, high local concentrations of biological targets are required to generate discernable MR contrast. We hypothesize that the prostate-specific membrane antigen (PSMA), an attractive target for imaging and therapy of prostate cancer, could serve as a suitable biomarker for MR-based molecular imaging. We have synthesized three new high-affinity, low-molecular-weight Gd(III) -based PSMA-targeted contrast agents containing one to three Gd(III) chelates per molecule. We evaluated the relaxometric properties of these agents in solution, in prostate cancer cells, and in an in vivo experimental model to demonstrate the feasibility of PSMA-based MR molecular imaging.Entities:
Keywords: cancer; gadolinium; imaging agents; magnetic resonance imaging
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Year: 2015 PMID: 26212031 PMCID: PMC4729199 DOI: 10.1002/anie.201503417
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336