Over the last decade, The University of Cincinnati College of Medicine has made a major commitment to studies of gene function. Our Transgenic and Knockout Mouse Core Facilities have produced over 600 transgenic mouse strains and over 100 knockout mouse strains. In 1996, a Gene Targeting Core Facility was established which in 1998 alone targeted 27 different genes. In addition, the College of Medicine was at the very forefront in developing Comparative Pathology and Mouse Physiology Core Facilities that have played essential roles in the characterization of dozens of transgenic and knockout strains with phenotypes ranging from preimplantation and congenital defects to cardiovascular disorders to cancer. More recently, an institutional focus on cancer has resulted in the recruitment of numerous clinical and basic science research faculty with outstanding research accomplishments, especially in the area of cancer genetics. With the institutional infrastructure for mouse genetics already in place, participation in the Mouse Models of Human Cancers Consortium will expand considerably our gene discovery and gene function research potential in the area of cancer biology. All of this, coupled with new focus on functional genomics, should give us the ability to make the most of our mouse models of human cancer and to contribute to the future of mouse modeling. We have proposed a focused plan to characterize, manipulate and develop new mouse models of gastrointestinal cancer. Through our participation in the Consortium, we hope to contribute our experience, models and new ideas in order to apply the next generation of functional genomics technologies, advances in drug and therapeutic protein discovery, and pharmacogenomics to the diagnosis and treatment of gastrointestinal cancer.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project--Cooperative Agreements (U01)
Project #
5U01CA084291-04
Application #
6514291
Study Section
Special Emphasis Panel (ZCA1-SRRB-7 (O3))
Program Officer
Marks, Cheryl L
Project Start
1999-09-30
Project End
2004-03-31
Budget Start
2002-06-08
Budget End
2003-03-31
Support Year
4
Fiscal Year
2002
Total Cost
$587,810
Indirect Cost
Name
University of Cincinnati
Department
Genetics
Type
Schools of Medicine
DUNS #
City
Cincinnati
State
OH
Country
United States
Zip Code
45221
Daniel, Scott G; Ball, Corbie L; Besselsen, David G et al. (2017) Functional Changes in the Gut Microbiome Contribute to Transforming Growth Factor ?-Deficient Colon Cancer. mSystems 2:
Caldwell, M E; DeNicola, G M; Martins, C P et al. (2012) Cellular features of senescence during the evolution of human and murine ductal pancreatic cancer. Oncogene 31:1599-608
Gopinathan, Aarthi; Denicola, Gina M; Frese, Kristopher K et al. (2012) Cathepsin B promotes the progression of pancreatic ductal adenocarcinoma in mice. Gut 61:877-84
Doetschman, Thomas; Georgieva, Teodora; Li, Hongqi et al. (2012) Generation of mice with a conditional allele for the transforming growth factor beta3 gene. Genesis 50:59-66
Doetschman, Thomas (2011) GI GEMs: genetically engineered mouse models of gastrointestinal disease. Gastroenterology 140:380-385.e2
DeNicola, Gina M; Karreth, Florian A; Humpton, Timothy J et al. (2011) Oncogene-induced Nrf2 transcription promotes ROS detoxification and tumorigenesis. Nature 475:106-9
Doetschman, Thomas; Sholl, Allyson; Chen, Hwu dau rw et al. (2011) Divergent effects of calcineurin A? on regulatory and conventional T-cell homeostasis. Clin Immunol 138:321-30
Nam, Ki Taek; Lee, Hyuk-Joon; Smith, J Joshua et al. (2010) Loss of Rab25 promotes the development of intestinal neoplasia in mice and is associated with human colorectal adenocarcinomas. J Clin Invest 120:840-9
Olive, Kenneth P; Jacobetz, Michael A; Davidson, Christian J et al. (2009) Inhibition of Hedgehog signaling enhances delivery of chemotherapy in a mouse model of pancreatic cancer. Science 324:1457-61
Karreth, Florian A; Tuveson, David A (2009) Modelling oncogenic Ras/Raf signalling in the mouse. Curr Opin Genet Dev 19:4-11

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