The Masonic Cancer Center (MCC) has been effective in its strategies to plan for and evaluate its mission The MCC has multiple internal and external resources for the planning and evaluation. Mechanisms for planning and evaluation include an External Advisory Board (EAB), Executive Committee with several subcommittees (Clinical and Translational Research Leadership, Science Council, Phase I Cancer Experimental Therapeutics Committee, Cancer Prevention and Control Steering Committee), Academic Health Center Planning and Reviews, Facility Planning Committees, and Minnesota Medical Foundation Capital Committee. MCC leaders and faculty also have leadership roles in other institutional units within the University. CCSG funds have and will be used to support the annual EAB meetings. In order to respond to the recommendations of the EAB and to increase the productivity of our basic, translational, and clinical research endeavors, the MCC holds periodic retreats and other meetings to develop strategic plans and goals. In the past funding period, we set the following strategic priorities and took steps to address each of them. ? Expand the resources for translational research ? Develop mechanisms to support the development of multi-investigator grants to expand translational capabilities ? Increase research capabilities by expanding research space and recruiting new laboratory-based investigators ? Create a new Cancer Detection, Treatment, and Survivorship (CaDeTS) research program or focus ? Refocus the Tumor Biology and Progression Program and the Women's Cancer Programs ? Integrate the Oncology Service Line into MCC operations and leadership, leveraging the research programs, clinical expertise, and resources ? Support health disparities research with MCC resources

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA077598-16
Application #
8633139
Study Section
Subcommittee G - Education (NCI)
Project Start
1998-06-01
Project End
2019-01-31
Budget Start
2014-03-05
Budget End
2015-01-31
Support Year
16
Fiscal Year
2014
Total Cost
$70,118
Indirect Cost
$61,605
Name
University of Minnesota Twin Cities
Department
Type
DUNS #
555917996
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
Sarver, Aaron L; Murray, Collin D; Temiz, Nuri A et al. (2016) MYC and PVT1 synergize to regulate RSPO1 levels in breast cancer. Cell Cycle 15:881-5
Diep, Caroline H; Knutson, Todd P; Lange, Carol A (2016) Active FOXO1 Is a Key Determinant of Isoform-Specific Progesterone Receptor Transactivation and Senescence Programming. Mol Cancer Res 14:141-62
Yun, Young Sung; Kim, Kwan Hyun; Tschida, Barbara et al. (2016) mTORC1 Coordinates Protein Synthesis and Immunoproteasome Formation via PRAS40 to Prevent Accumulation of Protein Stress. Mol Cell 61:625-39
Yan, Y; Hanse, E A; Stedman, K et al. (2016) Transcription factor C/EBP-β induces tumor-suppressor phosphatase PHLPP2 through repression of the miR-17-92 cluster in differentiating AML cells. Cell Death Differ 23:1232-42
Beura, Lalit K; Hamilton, Sara E; Bi, Kevin et al. (2016) Normalizing the environment recapitulates adult human immune traits in laboratory mice. Nature 532:512-6
Than, B L N; Linnekamp, J F; Starr, T K et al. (2016) CFTR is a tumor suppressor gene in murine and human intestinal cancer. Oncogene 35:4179-87
Struntz, Nicholas B; Harki, Daniel A (2016) Catch and Release DNA Decoys: Capture and Photochemical Dissociation of NF-κB Transcription Factors. ACS Chem Biol 11:1631-8
Knorr, David A; Wang, Hongbo; Aurora, Mukta et al. (2016) Loss of T Follicular Helper Cells in the Peripheral Blood of Patients with Chronic Graft-versus-Host Disease. Biol Blood Marrow Transplant 22:825-33
Glasgow, Michelle; Vogel, Rachel Isaksson; Burgart, Jennifer et al. (2016) Long term follow-up of a phase II trial of multimodal therapy given in a ""sandwich"" method for stage III, IV, and recurrent endometrial cancer. Gynecol Oncol Res Pract 3:6
Felices, Martin; Lenvik, Todd R; Davis, Zachary B et al. (2016) Generation of BiKEs and TriKEs to Improve NK Cell-Mediated Targeting of Tumor Cells. Methods Mol Biol 1441:333-46

Showing the most recent 10 out of 763 publications