The function of this Shared Resource is to provide an efficient, economical and effective use of animals for the performance of cancer-related studies. A significant emphasis is placed on the use of immunocompromised rodents. Major services provided by the Animal Research Resource include: animal purchase requests; inoculation of animals; propagation of tumor cell lines in animals; measurement of tumors; administration of carcinogens, s and hormonal agents; and necropsy. A service for the production of rabbit polyclonal antisera is also provided. Two additional rooms are also maintained to NIH Biosafety Level II standards for investigators using retroviral vectors and chemical carcinogens. Small transgenic breeding colonies are also maintained and a new transgenic Service has been established within the Resource, co-directed by Drs. Clarke and Dickson. The Shared resource is located within the Georgetown University Medical Center Research Resources Facility (RR). The is a centralized, AAALAC accredited and USDA registered research facility. All cell lines for inoculation require evidence of current murine antibody production test status. The general environment and animal health is monitored by the use of sentinel mice maintained in each colony room. All immunocompromised rodents are maintained within a viral antibody free environment. The services of this Resource are critical to the effective and economical use of animals by LCC investigators. The highly trained and experienced technical staff work closely with Cancer Center members to provide quality animal care and technical services in support of peer reviewed projects requiring the use of animals. Continuing increases in demand has required an increase in space to maintain rodents. We anticipate a further 50 percent increase in usage over the next five year period. The space requirements will be met with an ongoing RRF expansion. In 1995, the Shared Resource was utilized by 24 cancer center members m eight programs. 96 % of the projects utilizing the Shared Resource were supported by peer

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA051008-09
Application #
6102584
Study Section
Project Start
1998-05-15
Project End
1999-04-30
Budget Start
Budget End
Support Year
9
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Georgetown University
Department
Type
DUNS #
049515844
City
Washington
State
DC
Country
United States
Zip Code
20057
Naab, Tammey J; Gautam, Anita; Ricks-Santi, Luisel et al. (2018) MYC amplification in subtypes of breast cancers in African American women. BMC Cancer 18:274
Alamri, Ahmad M; Liu, Xuefeng; Blancato, Jan K et al. (2018) Expanding primary cells from mucoepidermoid and other salivary gland neoplasms for genetic and chemosensitivity testing. Dis Model Mech 11:
Nomura, Sarah J O; Hwang, Yi-Ting; Gomez, Scarlett Lin et al. (2018) Dietary intake of soy and cruciferous vegetables and treatment-related symptoms in Chinese-American and non-Hispanic White breast cancer survivors. Breast Cancer Res Treat 168:467-479
Hinzman, Charles P; Baulch, Janet E; Mehta, Khyati Y et al. (2018) Exposure to Ionizing Radiation Causes Endoplasmic Reticulum Stress in the Mouse Hippocampus. Radiat Res 190:483-493
Lelo, Alana; Prip, Frederik; Harris, Brent T et al. (2018) STAG2 Is a Biomarker for Prediction of Recurrence and Progression in Papillary Non-Muscle-Invasive Bladder Cancer. Clin Cancer Res 24:4145-4153
Tassi, Elena; Lai, En Yin; Li, Lingli et al. (2018) Blood Pressure Control by a Secreted FGFBP1 (Fibroblast Growth Factor-Binding Protein). Hypertension 71:160-167
Burks, Julian; Nadella, Sandeep; Mahmud, Abdullah et al. (2018) Cholecystokinin Receptor-Targeted Polyplex Nanoparticle Inhibits Growth and Metastasis of Pancreatic Cancer. Cell Mol Gastroenterol Hepatol 6:17-32
Kumar, Santosh; Suman, Shubhankar; Fornace Jr, Albert J et al. (2018) Space radiation triggers persistent stress response, increases senescent signaling, and decreases cell migration in mouse intestine. Proc Natl Acad Sci U S A 115:E9832-E9841
Choudhary, Saba; Ramasundaram, Poornema; Dziopa, Eugenia et al. (2018) Human ex vivo 3D bone model recapitulates osteocyte response to metastatic prostate cancer. Sci Rep 8:17975
Sponholtz, Todd R; Palmer, Julie R; Rosenberg, Lynn A et al. (2018) Exogenous Hormone Use and Endometrial Cancer in U.S. Black Women. Cancer Epidemiol Biomarkers Prev 27:558-565

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