The commercially available Focus is a dedicated ultra-high-resolution small-animal 3D positron emission tomograph (PET) (Concorde Microsystems) employing lutetium ortho-oxysilicate (LSO) detector blocks. The LSO blocks in the Focus are unique in that the spacing between adjacent crystal elements (approximately 1x1 mm) is significantly narrower than in other systems, yielding significantly improved spatial resolution approximately- 1 mm (volume resolution: 1 mm3 - 10-fold better than current-generation microPETs). We have had 3 years experience with Concorde's older-design R4 microPET -resulting in 23 publications and 25 abstracts. Although very useful, the R4 has serious limitations for quantification in mouse tumor models (xenograft, transgenic, and knock-out). Our microPET users will thus greatly benefit from the state-of-the-art capabilities offered by the Focus - besides providing badly needed additional microPET imaging time for our many funded studies that involve imaging of radiotracers. We believe that we are well suited by experience and expertise to fully exploit the capabilities of the Focus. In addition, a well-established infrastructure is already in place to provide and coordinate the necessary logistical, technical, and scientific components critical to a successful small-animal imaging program. For example, the Cyclotron and Radiochemistry Core Laboratory includes our new (but fully operational) dual-beam, 19/9 Ebco cyclotron, producing a broad array of positron-emitting radionuclides (eg carbon-11, fluorine-18, gallium-66, yttium-86, iodine-124 etc) and radiotracers (e.g. C11-colchicine and -methionine, F18-FMiso, -FEAU, and -FDHT, Ga66-DOTATOC, Y86-DOTA-Biotin, and I124-FIAU and IAZG). Using such multiple radiotracers, regional tumor perfusion, metabolism, receptor and antigen levels, hypoxia, and gene expression can be assessed serially by microPET in the same animal - prior to, during, and after treatment, including the many novel drug, radiation, and radionuclide therapies being developed at MSKCC. In summary, the Animal Imaging Core Facility at MSKCC is being utilized by a continually expanding number of funded investigators and molecular imaging has emerged as a critical component of our research armamentarium. Acquisition of the state-of-the-art Focus will be an invaluable adjunct to resources already in place, and will further enhance our Center-wide, mission-critical capabilities in molecular imaging.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biomedical Research Support Shared Instrumentation Grants (S10)
Project #
1S10RR020892-01
Application #
6877589
Study Section
Special Emphasis Panel (ZRG1-SBIB-H (30))
Program Officer
Tingle, Marjorie
Project Start
2005-01-15
Project End
2007-01-31
Budget Start
2005-01-15
Budget End
2007-01-31
Support Year
1
Fiscal Year
2005
Total Cost
$499,000
Indirect Cost
Name
Sloan-Kettering Institute for Cancer Research
Department
Type
DUNS #
064931884
City
New York
State
NY
Country
United States
Zip Code
10065
Lee, Jason T; Moroz, Maxim A; Ponomarev, Vladimir (2018) Imaging T Cell Dynamics and Function Using PET and Human Nuclear Reporter Genes. Methods Mol Biol 1790:165-180
McDevitt, Michael R; Thorek, Daniel L J; Hashimoto, Takeshi et al. (2018) Feed-forward alpha particle radiotherapy ablates androgen receptor-addicted prostate cancer. Nat Commun 9:1629
Moroz, Maxim A; Zanzonico, Pat; Lee, Jason T et al. (2018) Ex Vivo Radiolabeling and In Vivo PET Imaging of T Cells Expressing Nuclear Reporter Genes. Methods Mol Biol 1790:153-163
Keinänen, Outi; Fung, Kimberly; Pourat, Jacob et al. (2017) Pretargeting of internalizing trastuzumab and cetuximab with a 18F-tetrazine tracer in xenograft models. EJNMMI Res 7:95
Pankov, Dmitry; Sjöström, Ludvig; Kalidindi, Teja et al. (2017) In vivo immuno-targeting of an extracellular epitope of membrane bound preferentially expressed antigen in melanoma (PRAME). Oncotarget 8:65917-65931
Russell, James; Pillarsetty, Nagavarakishore; Kramer, Robin M et al. (2017) In Vitro and In Vivo Comparison of Gemcitabine and the Gemcitabine Analog 1-(2'-deoxy-2'-fluoroarabinofuranosyl) Cytosine (FAC) in Human Orthotopic and Genetically Modified Mouse Pancreatic Cancer Models. Mol Imaging Biol 19:885-892
Lee, Jason T; Zhang, Hanwen; Moroz, Maxim A et al. (2017) Comparative Analysis of Human Nucleoside Kinase-Based Reporter Systems for PET Imaging. Mol Imaging Biol 19:100-108
Brand, Christian; Longo, Valerie A; Groaning, Mike et al. (2017) Development of a New Folate-Derived Ga-68-Based PET Imaging Agent. Mol Imaging Biol 19:754-761
Doran, Michael G; Carnazza, Kathryn E; Steckler, Jeffrey M et al. (2016) Applying ??Zr-Transferrin To Study the Pharmacology of Inhibitors to BET Bromodomain Containing Proteins. Mol Pharm 13:683-8
Thorek, Daniel L J; Watson, Philip A; Lee, Sang-Gyu et al. (2016) Internalization of secreted antigen-targeted antibodies by the neonatal Fc receptor for precision imaging of the androgen receptor axis. Sci Transl Med 8:367ra167

Showing the most recent 10 out of 21 publications