The goal of the University of Chicago Cancer Research Center (UCCRC) Animal Barrier Facilities is to provide Cancer Center members the ability to conduct studies with rodents free of intercurrent infection with adventitious murine pathogens. The Barriers are supported by the facilities, programs, and staff of the University's Animal Resources Center (ARC). The ARC's Comparative Diagnostic Laboratory(CDL) provides expertise in rodent serology, microbiology, parasitology, and hematology. All biological materials introduced into rodents maintained in these facilities are evaluated by the CDL for contamination with adventitious viruses and mycoplasma by MAP testing. The ARC conducts an extensive Murine Health Monitoring Program to confirm that the pathogen-free status of the barrier colonies are maintained. The program is designed to detect variance in health status at specific time intervals. The program employs sentinel animals monitored monthly, serum banking, evaluation of """"""""index"""""""" cases and close communication with investigative staff who may note unexplained variances in their experiments. Additionally, a quarantine program which includes extensive diagnostic evaluation is instituted for all rodents imported from colonies obtained from non-commercial vendors. Quarantine is essential to minimize the likelihood of introducing unwanted murine pathogens into barrier colonies. The rodent barrier facilities serving the UCCRC are located on the top floor of the Franklin McLean Institute (FMI) and in the basement of Biological Sciences Learning Center (BSLC). They are essential components of the Cancer Research Center, providing approximately 7,925 net square feet of animal holding and procedure space. The facilities contain sixteen animal holding rooms, seven of which are equipped with three Illinois cubicles. In addition to animal holding rooms, the barriers are equipped with laboratory and procedure space. Isolator type caging systems are employed throughout the barriers. All caging materials and feed are autoclaved prior to use. Animals are transferred within a separate hood or within a cubicle by animal care specialists, using chemically disinfected forceps between cage transfers. A maximum of four or five mice, dependent on weight, are permitted per cage. A bar coded cage card provides encrypted information including the strain or stock, source, and investigator. Cage cards are routinely scanned for information which is downloaded into the ARC database that is used to maintain accurate and detailed census information.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
3P30CA014599-26S1
Application #
6396727
Study Section
Project Start
1999-08-01
Project End
2000-07-31
Budget Start
Budget End
Support Year
26
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Chicago
Department
Type
DUNS #
225410919
City
Chicago
State
IL
Country
United States
Zip Code
60637
Lee, Ji-Hye; Park, Beom Seok; Han, Kang R et al. (2018) Insight Into the Interaction Between RNA Polymerase and VPg for Murine Norovirus Replication. Front Microbiol 9:1466
Cheng, Jason X; Chen, Li; Li, Yuan et al. (2018) RNA cytosine methylation and methyltransferases mediate chromatin organization and 5-azacytidine response and resistance in leukaemia. Nat Commun 9:1163
Johnson, Marianna B; Hoffmann, Joscelyn N; You, Hannah M et al. (2018) Psychosocial Stress Exposure Disrupts Mammary Gland Development. J Mammary Gland Biol Neoplasia 23:59-73
Sweis, Randy F; Zha, Yuanyuan; Pass, Lomax et al. (2018) Pseudoprogression manifesting as recurrent ascites with anti-PD-1 immunotherapy in urothelial bladder cancer. J Immunother Cancer 6:24
Kathayat, Rahul S; Cao, Yang; Elvira, Pablo D et al. (2018) Active and dynamic mitochondrial S-depalmitoylation revealed by targeted fluorescent probes. Nat Commun 9:334
Liu, Jun; Eckert, Mark A; Harada, Bryan T et al. (2018) m6A mRNA methylation regulates AKT activity to promote the proliferation and tumorigenicity of endometrial cancer. Nat Cell Biol 20:1074-1083
Bhanvadia, Raj R; VanOpstall, Calvin; Brechka, Hannah et al. (2018) MEIS1 and MEIS2 Expression and Prostate Cancer Progression: A Role For HOXB13 Binding Partners in Metastatic Disease. Clin Cancer Res 24:3668-3680
Wood, Kevin; Byron, Elizabeth; Janisch, Linda et al. (2018) Capecitabine and Celecoxib as a Promising Therapy for Thymic Neoplasms. Am J Clin Oncol 41:963-966
Sample, Ashley; Zhao, Baozhong; Wu, Chunli et al. (2018) The Autophagy Receptor Adaptor p62 is Up-regulated by UVA Radiation in Melanocytes and in Melanoma Cells. Photochem Photobiol 94:432-437
Hrusch, C L; Manns, S T; Bryazka, D et al. (2018) ICOS protects against mortality from acute lung injury through activation of IL-5+ ILC2s. Mucosal Immunol 11:61-70

Showing the most recent 10 out of 668 publications