This Core now supports basic, translational and clinical research. The Flow Cytometry and Immune Monitoring Core Facility has been broadened to include an immune monitoring component to provide stateof- the-art technologies for cellular and serum analysis available to Cancer Center investigators with interest in basic science or clinical applications. Since the last submission the Flow Cytometry component has acquired two new state-of-the-art instruments: a dual laser high speed digital cell sorter and a dual laser analyzer. With this instrumentation the Core is able to accommodate the increasing applications that investigators request. The personnel managing this facility have served Cancer Center members for over 20 years. In the last year the Facility was utilized by 32 different Cancer Center members that represent an increase of 60% over the previous grant submission. These investigators accounted for 88% of the Facilities total usage. The new Immune Monitoring component offers services to investigators engaged in clinical immunotherapy trials. These include cancer vaccines or cytokines, or clinical trials in which the immune status of the patient might provide predictive or diagnostic information. An example of the latter is cytokine levels that might be linked to a disease outcome. In addition, this component will also assist preclinical researchers that want to analyze immune responses in animal (tumor) models. The services include the current standard for immune monitoring: the ELISPOT assay for detection of cytokines released by activated T cells, intracellular cytokine staining, enumeration of T cells by tetramer analysis, a multiplex assay for detection of up to 13 cytokines as well as radioisotope-based proliferation and cytotoxicity assays. Another critical service the core provides is the standardized isolation of serum and cells from (apheresed) blood specimens and freezing and storing the cells for later analyses. Both components are evaluated by a common User Committee. The Immune Monitoring facility is being set up with a $1M investment in equipment, maintenance contracts and pilot research projects through the Mabel and Arnold Beckman Foundation. No support for the Immune Monitoring component is requested until year 2 when the Beckman foundation grant expires.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA014089-35
Application #
8056483
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2009-12-01
Budget End
2010-11-30
Support Year
35
Fiscal Year
2010
Total Cost
$95,870
Indirect Cost
Name
University of Southern California
Department
Type
DUNS #
072933393
City
Los Angeles
State
CA
Country
United States
Zip Code
90089
McSkane, Michelle; Stintzing, Sebastian; Heinemann, Volker et al. (2018) Association Between Height and Clinical Outcome in Metastatic Colorectal Cancer Patients Enrolled Onto a Randomized Phase 3 Clinical Trial: Data From the FIRE-3 Study. Clin Colorectal Cancer 17:215-222.e3
Khanova, Elena; Wu, Raymond; Wang, Wen et al. (2018) Pyroptosis by caspase11/4-gasdermin-D pathway in alcoholic hepatitis in mice and patients. Hepatology 67:1737-1753
Brunette, Laurie L; Mhawech-Fauceglia, Paulette Y; Ji, Lingyun et al. (2018) Validity and prognostic significance of sperm protein 17 as a tumor biomarker for epithelial ovarian cancer: a retrospective study. BMC Cancer 18:970
Tokunaga, Ryuma; Cao, Shu; Naseem, Madiha et al. (2018) Prognostic Effect of Adenosine-related Genetic Variants in Metastatic Colorectal Cancer Treated With Bevacizumab-based Chemotherapy. Clin Colorectal Cancer :
Lang, Julie E; Brownson, Kirstyn E (2018) ASO Author Reflections: The Whole Transcriptome Landscape of Circulating Tumor Cells in Nonmetastatic Breast Cancer. Ann Surg Oncol :
Poulard, Coralie; Baulu, Estelle; Lee, Brian H et al. (2018) Increasing G9a automethylation sensitizes B acute lymphoblastic leukemia cells to glucocorticoid-induced death. Cell Death Dis 9:1038
Guo, Yu; Perez, Andrew A; Hazelett, Dennis J et al. (2018) CRISPR-mediated deletion of prostate cancer risk-associated CTCF loop anchors identifies repressive chromatin loops. Genome Biol 19:160
Milam, Joel; Slaughter, Rhona; Tobin, Jessica L et al. (2018) Childhood Cancer Survivorship and Substance Use Behaviors: A Matched Case-Control Study Among Hispanic Adolescents and Young Adults. J Adolesc Health 63:115-117
Singh, Hardeep P; Wang, Sijia; Stachelek, Kevin et al. (2018) Developmental stage-specific proliferation and retinoblastoma genesis in RB-deficient human but not mouse cone precursors. Proc Natl Acad Sci U S A 115:E9391-E9400
Suenaga, Mitsukuni; Schirripa, Marta; Cao, Shu et al. (2018) Potential role of PIN1 genotypes in predicting benefit from oxaliplatin-based and irinotecan-based treatment in patients with metastatic colorectal cancer. Pharmacogenomics J 18:623-632

Showing the most recent 10 out of 842 publications