Vascular targeting is a promising new strategy for detecting and treating solid tumors but a thorough assessment of the localization and processing of potential tumor targeting probes by tumor vessels is key to prioritizing candidate targets for future basic and clinical study. Imaging in this core will range from the whole body level to the tissue/cell level to subcellular elements and will include both static """"""""snap shots"""""""" as well as dynamic, real-time, continuous visualization of probe targeting and processing. The Imaging Core Facility will provide the necessary equipment and expertise to enable Program Project Investigators to obtain key information about their most promising candidates quickly and in a cost-effective manner. The services provided by the core include: 1) Cutting of tissue sections of human, rat, and mouse samples for light, fluorescence, and electron microscopy; 2) Providing assistance, and/or directly processing, rat and mouse tissue/tumors for localization of targets and targeting probes and evaluation of tissue damage after treatment; 3) Providing supervised or direct assistance in operating the imaging equipment (SPECT camera and light, fluorescence, deconvolution, and electron microscopes); 4) Providing sound expert advise to all PPG participants in performing all aspects of imaging necessary for each of the projects and to assist in imaging data analysis and interpretation; and 5) Producing the probes necessary for the imaging studies, including fluorophore and colloidal gold conjugations, biotinylations, and radioactive labeling. The Imaging Core will be directed by Dr. Jan Schnitzer (Program Director), who has over 20 years experience in all aspects of digital and microscopic imaging, and will be dedicated to providing all participating scientists with an easily accessible, user-friendly, and state-of-the-art facility for imaging the targeting, processing, and efficacy of tumor-homing probes.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA104898-03
Application #
7455276
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2007-05-01
Budget End
2008-04-30
Support Year
3
Fiscal Year
2007
Total Cost
$271,017
Indirect Cost
Name
Sidney Kimmel Cancer Center
Department
Type
DUNS #
789644697
City
San Diego
State
CA
Country
United States
Zip Code
92121
Oh, Phil; Testa, Jacqueline E; Borgstrom, Per et al. (2014) In vivo proteomic imaging analysis of caveolae reveals pumping system to penetrate solid tumors. Nat Med 20:1062-8
Sawada, Junko; Urakami, Takeo; Li, Fangfei et al. (2012) Small GTPase R-Ras regulates integrity and functionality of tumor blood vessels. Cancer Cell 22:235-49
Chrastina, Adrian; Schnitzer, Jan E (2012) Laser-targeted photosensitizer-induced lung injury: noninvasive rat model of pulmonary infarction. Exp Lung Res 38:1-8
Weis, Sara M; Cheresh, David A (2011) ?V integrins in angiogenesis and cancer. Cold Spring Harb Perspect Med 1:a006478
Shields, D J; Murphy, E A; Desgrosellier, J S et al. (2011) Oncogenic Ras/Src cooperativity in pancreatic neoplasia. Oncogene 30:2123-34
Murphy, Eric A; Majeti, Bharat K; Mukthavaram, Rajesh et al. (2011) Targeted nanogels: a versatile platform for drug delivery to tumors. Mol Cancer Ther 10:972-82
Chrastina, Adrian; Massey, Kerri A; Schnitzer, Jan E (2011) Overcoming in vivo barriers to targeted nanodelivery. Wiley Interdiscip Rev Nanomed Nanobiotechnol 3:421-37
Mielgo, Ainhoa; Seguin, Laetitia; Huang, Miller et al. (2011) A MEK-independent role for CRAF in mitosis and tumor progression. Nat Med 17:1641-5
Murphy, Eric A; Shields, David J; Stoletov, Konstantin et al. (2010) Disruption of angiogenesis and tumor growth with an orally active drug that stabilizes the inactive state of PDGFRbeta/B-RAF. Proc Natl Acad Sci U S A 107:4299-304
Akbulut, H; Tang, Y; Akbulut, K G et al. (2010) Addition of adenoviral vector targeting of chemotherapy to the MUC-1/ecdCD40L VPPP vector prime protein boost vaccine prolongs survival of mice carrying growing subcutaneous deposits of Lewis lung cancer cells. Gene Ther 17:1333-40

Showing the most recent 10 out of 38 publications