The overall goal of the Transgenic/Knockout Rodent Core offers state-of-the-art services for the manipulation of mouse and rat genomes, ensuring that the primary beneficiaries of CCSG-supported Shared Resources have the best information and technical resources available to support cancer research. The Core, which is Cancer Center managed, was established in 1993 to produce transgenic and knockout mice for USC Norris members and to increase the use of mouse technology through education and consultation to the cancer research community. Since its inception, the Core has operated under the same faculty leader, Dr. Robert Maxson, and manager, Dr. Nancy Wu; it has also been continuously funded by the CCSG. The Core is widely recognized within the USC community and beyond for the high quality of its services. The Core produces transgenic and knockout mice and offers two important new services, knockout rats and CRISPR/Cas9- mediated gene editing in mice. Using ES cell technology pioneered by Dr. Qi-Long Ying at USC, the Core generated the first knockout rats. The new CRISPR/Cas9 technology will make it possible to produce gene knockouts much faster and at lower cost than current ES cell-based technology. The Core continues to be active in education and consulting services, and provides a number of important ancillary services, including in vitro fertilization, and re-derivation of mouse strains, as well as cryopreservation of embryos. At the last CCSG renewal, the Core received a merit rating of ?excellent? with reviewers noting the competence of the Core leadership and the high quality of the work. The only criticism was low usage by Cancer Center members, although it was recognized that the Core serves the entire USC community. We have stepped up efforts to promote the availability of the Core and encourage cancer investigators to use Core services in their research. In the most recent year, 12 peer-review funded members, or 71% of total users, from four Research Programs (Epigenetics and Regulation, Gastrointestinal Cancers, Molecular Genetics, and Tumor Microenvironment) used the Core to accomplish their research objectives.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA014089-45
Application #
9838166
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2019-12-01
Budget End
2020-11-30
Support Year
45
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Southern California
Department
Type
DUNS #
072933393
City
Los Angeles
State
CA
Country
United States
Zip Code
90089
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
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
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
Kiran, Sayee; Jeong, Young Ju; Nelson, Maria E et al. (2018) Are we overtreating intraductal papillomas? J Surg Res 231:387-394
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:

Showing the most recent 10 out of 842 publications