SMALL ANIMAL IMAGING SHARED RESOURCE (SAISR) ABSTRACT The Small Animal Imaging Shared Resource (SAISR) provides instrumentation, training, and expert support for imaging studies conducted by UCLA Jonsson Comprehensive Cancer Center (JCCC) investigators. Major technologies and services include micro-positron emission tomography (microPET), invented at SAISR, micro- computed tomography (microCT), optical imaging (bioluminescence, fluorescence and Cerenkov), autoradiography imaging, and routine production of small molecule radiochemistry and peptide/protein radiolabeling. SAISR has a biomedical cyclotron, biomolecule radiolabeling facility, and a fully equipped radiochemistry facility with state-of-the-art radiosynthesizers specifically designed to support PET imaging.
Three specific aims support the SAISR objective of providing investigators with technical imaging expertise and facilitating the design, execution, and analysis of small animal imaging studies.
Aim 1 : to provide and support state-of-the-art small animal imaging technologies;
Aim 2 : to provide routine radiochemistry and radiolabeling production services;
and Aim 3 : to provide investigators with scientific support and training in radiochemistry, preclinical imaging, and image analysis. Monthly two-hour training sessions educate users on the latest imaging technologies and approaches, including topics on instrumentation basics, imaging biology, imaging procedures, and safety protocols. Examples of SAISR impact in the prior project period include SAISR support for David Nathanson, PhD (CMINT) in developing novel combination therapies to target tumor metabolism in glioblastoma multiforme (GBM). PET/CT imaging of rapid changes in GBM glucose utilization by [18F]FDG, a biomarker of glycolysis, effectively predict therapeutic responses in vivo and is currently being tested in a clinical trial (NCT03732352). PET and MRI imaging enabled a large inter-programmatic team led by Robert Prins, PhD (CMINT/TI) to differentiate inflammatory responses in GBM by PET from other sources of contrast-enhancement seen by MRI. The combination of these two imaging modalities distinguished tumor progression from pseudoprogression in immunotherapy. In a collaboration between SAISR and JCCC Molecular Screening Shared Resource (MSSR), an inter-programmatic team led by Caius Radu, MD (CMINT) developed a combination therapy targeting deoxycytidine kinase (dCK) using [18F]FAC PET to assess the pharmacodynamics of novel dCK inhibitors. Follow-on PET studies showed that dCK contributes to radiation resistance in cancer. From 2013 ? 2018, SAISR supported projects from 42 JCCC members in all six Programs, representing 84% of SAISR usage. Of this, 53% of JCCC users had peer-reviewed funding. This resulted in 136 publications, with 73 (54%) in high-impact (IF ?10, or field leading) journals. The SAISR is preparing to submit an NIH shared instrumentation grant for a GNEXT PET/CT instrument, with the highest sensitivity currently available and based on technology invented by SAISR Director Arion Chatziioannou, PhD.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA016042-44
Application #
9936717
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2020-04-01
Budget End
2021-03-31
Support Year
44
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of California Los Angeles
Department
Type
DUNS #
092530369
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Tsang, Eric J; Wu, Benjamin; Zuk, Patricia (2018) MAPK signaling has stage-dependent osteogenic effects on human adipose-derived stem cells in vitro. Connect Tissue Res 59:129-146
Waters, Lynnea R; Ahsan, Fasih M; Wolf, Dane M et al. (2018) Initial B Cell Activation Induces Metabolic Reprogramming and Mitochondrial Remodeling. iScience 5:99-109
Van Dyk, Kathleen; Bower, Julienne E; Crespi, Catherine M et al. (2018) Cognitive function following breast cancer treatment and associations with concurrent symptoms. NPJ Breast Cancer 4:25
Robinett, Ryan A; Guan, Ning; Lux, Anja et al. (2018) Dissecting Fc?R Regulation through a Multivalent Binding Model. Cell Syst 7:41-48.e5
Chin, Chee Jia; Li, Suwen; Corselli, Mirko et al. (2018) Transcriptionally and Functionally Distinct Mesenchymal Subpopulations Are Generated from Human Pluripotent Stem Cells. Stem Cell Reports 10:436-446
Alban, Tyler J; Alvarado, Alvaro G; Sorensen, Mia D et al. (2018) Global immune fingerprinting in glioblastoma patient peripheral blood reveals immune-suppression signatures associated with prognosis. JCI Insight 3:
Yang, Qing; Fung, Wing K; Li, Gang (2018) Sample size determination for jointly testing a cause-specific hazard and the all-cause hazard in the presence of competing risks. Stat Med 37:1389-1401
Seo, Jai Woong; Tavaré, Richard; Mahakian, Lisa M et al. (2018) CD8+ T-Cell Density Imaging with 64Cu-Labeled Cys-Diabody Informs Immunotherapy Protocols. Clin Cancer Res 24:4976-4987
Ribas, Antoni; Wolchok, Jedd D (2018) Cancer immunotherapy using checkpoint blockade. Science 359:1350-1355
Wang, Hong; Chen, Xiaolin; Li, Gang (2018) Survival Forests with R-Squared Splitting Rules. J Comput Biol 25:388-395

Showing the most recent 10 out of 767 publications