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 #
5P30CA014089-33
Application #
7726551
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2007-12-01
Budget End
2008-11-30
Support Year
33
Fiscal Year
2008
Total Cost
$83,260
Indirect Cost
Name
University of Southern California
Department
Type
DUNS #
072933393
City
Los Angeles
State
CA
Country
United States
Zip Code
90089
Lu, Yingchang; Beeghly-Fadiel, Alicia; Wu, Lang et al. (2018) A Transcriptome-Wide Association Study Among 97,898 Women to Identify Candidate Susceptibility Genes for Epithelial Ovarian Cancer Risk. Cancer Res 78:5419-5430
Skeate, Joseph G; Da Silva, Diane M; Chavez-Juan, Elena et al. (2018) Nano-Pulse Stimulation induces immunogenic cell death in human papillomavirus-transformed tumors and initiates an adaptive immune response. PLoS One 13:e0191311
Kiran, Sayee; Jeong, Young Ju; Nelson, Maria E et al. (2018) Are we overtreating intraductal papillomas? J Surg Res 231:387-394
Liu, Gang; Mukherjee, Bhramar; Lee, Seunggeun et al. (2018) Robust Tests for Additive Gene-Environment Interaction in Case-Control Studies Using Gene-Environment Independence. Am J Epidemiol 187:366-377
Basso, Virginia; Garcia, Angie; Tran, Dat Q et al. (2018) Fungicidal Potency and Mechanisms of ?-Defensins against Multidrug-Resistant Candida Species. Antimicrob Agents Chemother 62:
Neumeyer, Sonja; Banbury, Barbara L; Arndt, Volker et al. (2018) Mendelian randomisation study of age at menarche and age at menopause and the risk of colorectal cancer. Br J Cancer 118:1639-1647
Ning, Y; Zhang, W; Hanna, D L et al. (2018) Clinical relevance of EMT and stem-like gene expression in circulating tumor cells of metastatic colorectal cancer patients. Pharmacogenomics J 18:29-34
Austria, Theresa; Marion, Christine; Yu, Vanessa et al. (2018) Mechanism of cytokinesis failure in ovarian cystadenomas with defective BRCA1 and P53 pathways. Int J Cancer 143:2932-2942
Zhang, Junjie; Zhao, Jun; Xu, Simin et al. (2018) Species-Specific Deamidation of cGAS by Herpes Simplex Virus UL37 Protein Facilitates Viral Replication. Cell Host Microbe 24:234-248.e5
Eriguchi, Yoshihiro; Nakamura, Kiminori; Yokoi, Yuki et al. (2018) Essential role of IFN-? in T cell-associated intestinal inflammation. JCI Insight 3:

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