Transgenic MouseMany in the biomedical sciences strongly believe that the progress of cancer research, and the position ofthe UCSD Cancer Center in the biomedical community during the next decade, will depend upon the abilityto use the mouse as an experimental model to investigate both basic and clinically relevant questions incancer research. The creation of new pre-clinical models of cancer in mice by genetic manipulation isspecifically cited by the NCI as one of four extraordinary opportunities they wish to exploit. Transgenic micecarrying new or novel genes are created by microinjection of DMA into the pronuclei of fertilized eggs and'knock-out' mice lacking specific genes of interest are created by homologous recombination in embryonicstem cells followed by injection into blastocysts to create chimeric mice for breeding to homozygosity. Thehigh degree of conservation of most sequences in genomes of humans and mice makes the idea of usingmouse genetic manipulation technology to create models of human cancer pathogenesis extremelyattractive. These approaches are remarkably powerful in cancer research particularly in the analysis ofoncogenes, metastasis, cell-cycle control, tumor suppressor genes, and in the crafting of cancer modelsystems for developing new treatment regimens, and methods for drug testing and tumor imaging. Themission of this Shared Resource is to provide the highly technical aspects of manipulation of genes inembryos and embryonic stem cells as a service to our Center members, allowing them to create thegenetically manipulated mouse models they need. This is an outstanding example of how specializedtechniques, highly trained dedicated personnel, and expensive equipment can be accessed by researcherswho could not reasonably expect to develop or obtain them on an individual basis. The availability of thisResource enables our researchers to conduct versatile, cutting-edge research with a battery of sophisticatedgenetic techniques.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA023100-23
Application #
7515276
Study Section
Subcommittee G - Education (NCI)
Project Start
2007-06-01
Project End
2012-04-30
Budget Start
2007-06-01
Budget End
2008-04-30
Support Year
23
Fiscal Year
2007
Total Cost
$257,070
Indirect Cost
Name
University of California San Diego
Department
Type
DUNS #
804355790
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Norton, Jeffrey A; Kim, Teresa; Kim, Joseph et al. (2018) SSAT State-of-the-Art Conference: Current Surgical Management of Gastric Tumors. J Gastrointest Surg 22:32-42
Ikeda, Sadakatsu; Tsigelny, Igor F; Skjevik, Åge A et al. (2018) Next-Generation Sequencing of Circulating Tumor DNA Reveals Frequent Alterations in Advanced Hepatocellular Carcinoma. Oncologist 23:586-593
Buckley, Alexandra R; Ideker, Trey; Carter, Hannah et al. (2018) Exome-wide analysis of bi-allelic alterations identifies a Lynch phenotype in The Cancer Genome Atlas. Genome Med 10:69
Parish, Austin J; Nguyen, Vi; Goodman, Aaron M et al. (2018) GNAS, GNAQ, and GNA11 alterations in patients with diverse cancers. Cancer 124:4080-4089
Xu, Selene; Thompson, Wesley; Ancoli-Israel, Sonia et al. (2018) Cognition, quality-of-life, and symptom clusters in breast cancer: Using Bayesian networks to elucidate complex relationships. Psychooncology 27:802-809
Tao, Li; Schwab, Richard B; San Miguel, Yazmin et al. (2018) Breast Cancer Mortality in Older and Younger Breast Cancer Patients in California. Cancer Epidemiol Biomarkers Prev :
Sagredo, Eduardo A; Blanco, Alejandro; Sagredo, Alfredo I et al. (2018) ADAR1-mediated RNA-editing of 3'UTRs in breast cancer. Biol Res 51:36
Ramdani, Ghania; Schall, Nadine; Kalyanaraman, Hema et al. (2018) cGMP-dependent protein kinase-2 regulates bone mass and prevents diabetic bone loss. J Endocrinol 238:203-219
Nguyen, Vi; Marmor, Rebecca A; Ramamoorthy, Sonia L et al. (2018) The Use of Solicited Publishing by Academic Surgeons. Surgery 164:212-218
Yan, Wei; Wu, Xiwei; Zhou, Weiying et al. (2018) Cancer-cell-secreted exosomal miR-105 promotes tumour growth through the MYC-dependent metabolic reprogramming of stromal cells. Nat Cell Biol 20:597-609

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