) UAB Cancer Center Members increasingly depend on important animal models of human malignancy for translational research. These include immunodeficient rodents, cancer-bearing rodents that may be immunocompromised by experimental therapies, and extremely valuable transgenic animals with a wide assortment of physiologic, immunologic or pathologic modifications. The Pathogen-Free Rodent Shared Facility provides a unique support mechanism which produces and maintains pathogen-free rodents of special strains and stocks for use in studies by members of the Cancer Center. Through a systematic program of controlled access to the facility, personnel training, health screening of incoming animals, and close monitoring of the health status of animal subpopulations, a shared facility for state-of-the-art pathogen-free rodent management is provided in the Cancer Center?s 5100 NSF animal facility.
The specific aims are: To provide a user-friendly, highly effective program for the provision of rodent animal models free of all indigenous pathogen infections for the support of translational research; To assist users of the Pathogen-Free Rodent Shared Facility in meeting their individual, often specialized, animal needs; To provide rigorous health screening of incoming animals, with quarantine in flexible film isolators at other campus locations until approved for entry into the shared facility; To closely monitor the health status of facility subpopulations, and to expeditiously remove, eliminate, or otherwise minimize the risks from animal stocks found to have significant pathogens, always in close consultation with investigators; and To closely supervise daily activities of the well qualified full-time Cancer Center animal husbandry staff selected for the facility in order to assure the consistent, high standard of animal care commensurate with the facility?s goals.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA013148-31
Application #
6605457
Study Section
Project Start
2002-07-02
Project End
2003-02-28
Budget Start
Budget End
Support Year
31
Fiscal Year
2002
Total Cost
$195,927
Indirect Cost
Name
University of Alabama Birmingham
Department
Type
DUNS #
004514360
City
Birmingham
State
AL
Country
United States
Zip Code
35294
Jimenez, Rachel V; Wright, Tyler T; Jones, Nicholas R et al. (2018) C-Reactive Protein Impairs Dendritic Cell Development, Maturation, and Function: Implications for Peripheral Tolerance. Front Immunol 9:372
Engle, Staci E; Antonellis, Patrick J; Whitehouse, Logan S et al. (2018) A CreER mouse to study melanin concentrating hormone signaling in the developing brain. Genesis 56:e23217
Van Arsdale, Anne R; Arend, Rebecca C; Cossio, Maria J et al. (2018) Insulin-like growth factor 2: a poor prognostic biomarker linked to racial disparity in women with uterine carcinosarcoma. Cancer Med 7:616-625
Kim, Harrison (2018) Modification of population based arterial input function to incorporate individual variation. Magn Reson Imaging 45:66-71
Leath 3rd, Charles A; Monk, Bradley J (2018) Twenty-first century cervical cancer management: A historical perspective of the gynecologic oncology group/NRG oncology over the past twenty years. Gynecol Oncol 150:391-397
Park, Misun; Yoon, Young Sup (2018) Cardiac Regeneration with Human Pluripotent Stem Cell-Derived Cardiomyocytes. Korean Circ J 48:974-988
Toboni, Michael D; Smith, Haller J; Bae, Sejong et al. (2018) Predictors of Unplanned Reoperation for Ovarian Cancer Patients From the National Surgical Quality Improvement Program Database. Int J Gynecol Cancer 28:1427-1431
Dionne-Odom, J Nicholas; Applebaum, Allison J; Ornstein, Katherine A et al. (2018) Participation and interest in support services among family caregivers of older adults with cancer. Psychooncology 27:969-976
Demark-Wahnefried, Wendy; Schmitz, Kathryn H; Alfano, Catherine M et al. (2018) Weight management and physical activity throughout the cancer care continuum. CA Cancer J Clin 68:64-89
Bandari, Shyam K; Purushothaman, Anurag; Ramani, Vishnu C et al. (2018) Chemotherapy induces secretion of exosomes loaded with heparanase that degrades extracellular matrix and impacts tumor and host cell behavior. Matrix Biol 65:104-118

Showing the most recent 10 out of 747 publications