Julie L. Sutcliffe, Ph.D.

Department of Internal Medicine, Division of Hematology and Oncology, UC Davis
Department of Biomedical Engineering,

IRC Building (#41)
Room 1763
2921 Stockton Blvd
Sacramento, CA 95817

Phone: (916) 734-5536
Fax: (916) 734-7572

Email: jlsutcliffe@ucdavis.edu
WWW: http://bme.ucdavis.edu/sutcliffe/

Development of Novel Imaging Probes and Chemistries for PET

Dr. Sutcliffe’s research involves the design, synthesis and in vivo evaluation of targeted molecular imaging agents with a focus on positron emission tomography (PET). Her group has developed rapid radiolabeling technologies using both solid-phase and solution-phase chemistries to incorporate the short half-life PET radionuclide fluorine-18 into peptides. Peptide based radiopharmaceuticals are gaining extensive attention as targeted molecular imaging agents. It is therefore important that technologies are developed that allow these agents to be synthesized rapidly and screened both in vitro and in vivoto assess their efficacy.

Her group applies radiolabeled peptides to target cell surface receptors in vivo using small animal imaging. Major cell surface receptors of interest include the integrin receptors alpha(v)beta(3) and alpha(v)beta(6). Integrins are cell surface glycoproteins involved in cell-cell and cell- extracellular matrix interactions. Their over expression has been associated with many diseases including cancer. In particular alpha(v)beta(6) is expressed at low or undetectable levels on normal tissue and is upregulated on many cancers including oral squamous cell carcinoma, breast cancer, pancreatic cancer and has recently been identified as a marker of prognosis in colon and lung cancer. In vivo imaging of this receptor could therefore have a significant impact on patient diagnosis, care and management.

Dr Sutcliffe’s group uses two approaches to develop targeted molecular imaging agents to image cell surface receptors: A “rational approach” based on known binding structures and a “random approach” using the one-bead-one-compound molecular library methodology. Peptides are synthesized using standard Fmoc chemistries, screened in vitro for affinity and selectivity and subsequently radiolabeled and screened in vivo using small animal imaging.

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