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Updated: May 21, 2026

MR Molecular Imaging of Prostate Cancer with a Small Molecular CLT1 Peptide Targeted Contrast Agent
Published on: September 3, 2013
Prostate-specific membrane antigen-based imaging
Joseph R Osborne1, Naveed H Akhtar, Shankar Vallabhajosula
1Department of Radiology, Weill Cornell Medical College, New York, NY 10065, USA.
Prostate cancer (CaP) imaging can be improved by targeting prostate-specific membrane antigen (PSMA). New agents, including antibodies and small molecules, show promise for more sensitive and specific CaP detection and management.
Area of Science:
- Oncology
- Radiology
- Molecular Imaging
Background:
- Prostate cancer (CaP) is a common malignancy in North America.
- Conventional imaging lacks specificity for CaP, limiting patient management.
- Prostate-specific membrane antigen (PSMA) is overexpressed in CaP tissue.
Purpose of the Study:
- To explore novel imaging agents targeting PSMA for improved CaP detection.
- To evaluate the potential of antibodies and small molecules for PSMA-targeted imaging.
Main Methods:
- Review of existing PSMA-targeting agents, including antibodies (e.g., Hu mAb J591) and small molecules (e.g., MIP-1072, MIP-1095).
- Discussion of imaging characteristics, target binding, and potential for diagnostic applications using SPECT and PET.
Main Results:
- Humanized monoclonal antibodies (Hu mAb J591) show potential but have limitations in imaging speed.
- Small-molecule inhibitors (MIP-1072, MIP-1095) demonstrate high affinity for PSMA.
- (123)I-MIP-1072 and (123)I-MIP-1095 successfully imaged CaP xenografts, indicating suitability for human trials.
Conclusions:
- PSMA-targeted imaging agents, particularly small molecules, offer significant potential to enhance diagnostic sensitivity and specificity in prostate cancer.
- Further development of these agents could revolutionize CaP imaging and patient management.
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