Molecular-based imaging provides new opportunities to assess vital cellular processes in vivo. The ability tomonitor the molecular processes of cancer via non-invasive imaging may provide critical informationregarding the effects of therapy. In the context of pre-clinical research, the use of in vivo imaging permits theacquisition of a complete dynamic biodistribution study in each animal, thereby reducing the number ofanimals required to reach a statistically adequate result; often the techniques used in small animal imagingare directly transferable to the clinical setting. The Small Animal Imaging Core (SAIC) is a new sharedresource dedicated to providing investigators access to the state-of-the-art in small animal imagingcapabilities for use in basic and translational research relevant to the mission of the City of Hope CancerCenter.
Specific aims of the SAIC include: (1) maintaining a thorough understanding of the currentcapabilities and limitations of small animal imaging as they pertain to cancer research; (2) implementing,developing, calibrating, maintaining, and operating relevant imaging systems within the context of a smallanimal imaging laboratory; and (3) optimizing the use of small animal imaging in research at City of Hope byconsulting with investigators. Core personnel currently include a Director, an imaging physicist, and amanager, all of whom are highly experienced in the use of imaging for research with animals. Small animalimaging systems in operation include two units for bioluminescence optical imaging (I VIS 100, XenogenCorp.); a gamma camera (Y IMAGER, Biospace, Inc.); a PET scanner (microPET R4, CTIMI, Inc.); and a CTscanner (microCAT II Hi Res, CTIMI, Inc.). The microPET and microCAT are readily used in tandem togenerate co-registered functional-anatomic PET/CT images. The Animal Resources Center has providedfour rooms within the Parvin Biomedical Research Building for use by the animal imaging program (one roomfor the microPET, microCAT, and the y-IMAGER; two rooms for the Xenogen MS machines; and one roomfor a gamma counter). A system has been developed for billing users for a portion of the costs of the imagingprocedures. During the first 12-month reporting period, the SAIC was used by 13 Cancer Center membersfrom 3 Research Programs and peer-reviewed usage represented 89% of total usage. Annual budget for thecore is $165,922 (97% institution, 3% chargebacks); 42% ($70,000) is being requested from the CCSG.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA033572-25
Application #
7714127
Study Section
Subcommittee G - Education (NCI)
Project Start
2008-09-01
Project End
2012-11-30
Budget Start
2008-09-01
Budget End
2008-11-30
Support Year
25
Fiscal Year
2008
Total Cost
$49,650
Indirect Cost
Name
City of Hope/Beckman Research Institute
Department
Type
DUNS #
027176833
City
Duarte
State
CA
Country
United States
Zip Code
91010
Zhou, Jiehua; Lazar, Daniel; Li, Haitang et al. (2018) Receptor-targeted aptamer-siRNA conjugate-directed transcriptional regulation of HIV-1. Theranostics 8:1575-1590
Salgia, Ravi; Kulkarni, Prakash; Gill, Prakash S (2018) EphB4: A promising target for upper aerodigestive malignancies. Biochim Biophys Acta Rev Cancer 1869:128-137
Choi, Audrey H; O'Leary, Michael P; Lu, Jianming et al. (2018) Endogenous Akt Activity Promotes Virus Entry and Predicts Efficacy of Novel Chimeric Orthopoxvirus in Triple-Negative Breast Cancer. Mol Ther Oncolytics 9:22-29
Kumar, B; Garcia, M; Weng, L et al. (2018) Acute myeloid leukemia transforms the bone marrow niche into a leukemia-permissive microenvironment through exosome secretion. Leukemia 32:575-587
Dietze, Eric C; Chavez, Tanya A; Seewaldt, Victoria L (2018) Obesity and Triple-Negative Breast Cancer: Disparities, Controversies, and Biology. Am J Pathol 188:280-290
Ding, Yuan Chun; Adamson, Aaron W; Steele, Linda et al. (2018) Discovery of mutations in homologous recombination genes in African-American women with breast cancer. Fam Cancer 17:187-195
Kurata, Jessica S; Lin, Ren-Jang (2018) MicroRNA-focused CRISPR-Cas9 library screen reveals fitness-associated miRNAs. RNA 24:966-981
Hardwick, Nicola R; Frankel, Paul; Ruel, Christopher et al. (2018) p53-Reactive T Cells Are Associated with Clinical Benefit in Patients with Platinum-Resistant Epithelial Ovarian Cancer After Treatment with a p53 Vaccine and Gemcitabine Chemotherapy. Clin Cancer Res 24:1315-1325
Wussow, Felix; Chiuppesi, Flavia; Meng, Zhuo et al. (2018) Exploiting 2A peptides to elicit potent neutralizing antibodies by a multi-subunit herpesvirus glycoprotein complex. J Virol Methods 251:30-37
Kingsmore, Kathryn M; Vaccari, Andrea; Abler, Daniel et al. (2018) MRI analysis to map interstitial flow in the brain tumor microenvironment. APL Bioeng 2:

Showing the most recent 10 out of 1396 publications