Sutcliffe, Julie L. - University of California, Davis - Department of Biomedical Engineering

个人简介

Ph.D. in Medicinal Chemistry, 2002, King’s College, London

研究领域

Development of Targeted Molecular Imaging Agents Dr. Sutcliffe’s research involves the design, synthesis and in vivo evaluation of targeted molecular imaging agents with a focus on PET. Her group has developed rapid radiolabeling technologies using both solid-phase and solution-phase chemistries to incorporate the short half-life PET radionuclide 18F 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 vivo to 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.

近期论文

查看导师新发文章（温馨提示：请注意重名现象，建议点开原文通过作者单位确认）

MKJ Gagnon, SH Hausner, J Marik, CK Abbey, JF Marshall, JL Sutcliffe. High-throughput in vivo screening of targeted molecular imaging agents. Proceedings of the National Academy of Sciences. 106(42), 17904-17909. link SH Hausner, J Marik, MKJ Gagnon, JL Sutcliffe. In vivo positron emission tomography (PET) imaging with an alpha(v)beta(6) specific peptide radiolabeled using 18F-“click” chemistry: evaluation and comparison with the corresponding 4-[18F]fluorobenzoyl- and 2-[18F]fluoropropionyl-peptides. Journal of Medicinal Chemistry, 51(19), 5901-4. link CM Parsons, JL Sutcliffe, RJ Bold. Preoperative evaluation of pancreatic adenocarcinoma. Journal of Hepato-Biliary Pancreatic Surgery, 15, 429-35. link SH Hausner, D DiCara, J Marik, JF Marshall, JL Sutcliffe. Use of a peptide derived from foot-and-mouth-disease-virus (FMDV) for the non-invasive imaging of human cancer: Generation and evaluation of [18F]FBA-A20FMDV2 for in vivo imaging of integrin alpha(v)beta(6) expression with Positron Emission Tomography. Cancer Research, 67(16), 7833-40. link J Marik, JL Sutcliffe. Fully automated preparation of n.c.a. 4-[18F]fluorobenzoic acid and N-succinimidyl 4-[18F]fluorobenzoate using Siemens CTI/CPCU chemistry module. Applied Radiation and Isotopes, 65, 199-203. link J Marik, J L Sutcliffe. Click for PET: Rapid preparation of [18F]fluoropeptides using Cu(I) catalyzed 1,3-dipolar cycloaddition. Tetrahedron Letters, 47, 6681-4. J Marik, SH Hausner, LA Fix, MK Gagnon, JL Sutcliffe. Solid phase synthesis of 2-[18F]fluoropropionyl peptides. Bioconjugate Chemistry, 17, 1017-21. link