Flow cytometers and cell sorting instruments are required for many studies conducted by the investigators of the UCSD Cancer Center. However, the costs of purchasing, serving, and operating such complex instrument are beyond the capacity of most individual investigators. For this reason, a core resource in flow cytometry is essential. The speed at which these automated instruments can examine or separate free floating cell populations for several parameters simultaneously, and chart the results, has provided a powerful means for collecting data on cell populations of statistically reliable size. The magnetic sorting technology opens more opportunities for sorting living cells that are present as minor subpopulations, allowing for either studying them in isolation or after modification and re-infusion back into animal hosts. Without access to well-maintained and serviced instruments of this type and expert assistance in their use and interpretation of the results, may experiments that can provide valuable information would not be possible. Investigators who do not have such access to such facilities for appropriate work are handicapped in their opportunities to publish in reputable journals and in competitive grant applications. Together with the other shared resources which have been created at this Center, namely Molecular Pathology, Digital Imaging, and Histology, the resource participates in composing an exceptionally versatile analytical combination of services. The goal of this Resource is to expand the distinguished and reliable services it has given to the Translational Oncology and Molecular Virology Programs to accommodate the needs of the Cancer Genetics, Cancer Biology, Cancer Pharmacology, and Translational Oncology Programs.
Specific aims are to encourage and facilitate collaborations between Center members and to coordinate the work of the Resource with that of other Center resources wherever possible, to achieve enhancement of the research conducted by Members.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA023100-19
Application #
6599262
Study Section
Project Start
2002-06-11
Project End
2003-04-30
Budget Start
Budget End
Support Year
19
Fiscal Year
2002
Total Cost
$183,723
Indirect Cost
Name
University of California San Diego
Department
Type
DUNS #
077758407
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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