Mouse Modeling Mice are by far the most commonly used vertebrate research model organism for biomedical research, and the ability to generate efficiently genetically-engineered mouse models (GEMM), maintain those mice, and use them for sophisticated experimentation is the basis for the dominance of mice for mammalian biomedical research. As with most biomedical research platforms, the utilization of mice is complex, and often researchers need specialized support to accomplish their mouse experiments. The Mouse Modeling (MM) Shared Resource is focused on supporting researchers doing mouse experimentation by offering a broad range of services that are adapted for specific experimental needs, updating services with the latest technological approaches and doing this service in an efficient and cost-effective manner. By keeping the focus on flexibility, cutting-edge capability and efficiency of services, we have been able to support mouse model experimentation by many researchers and remain financially solvent for over 21 years. The vast majority of the experiments we support are cancer-focused, with other major areas including neuroscience, infectious disease and antibody generation. During the current award period services were performed for 27 Cancer Center Members, 25 of whom now are Members of all 4 NCCC Programs (CPS [1], CBT [11], ICI [10], and TEC [3]). NCCC Funded Members represented 37% of Total MM projects served (549), and we are requesting only 24% of the Total MM Operating Budget from CCSG support. As an example of value added to NCCC research, ?Floxed? ID2 mice were generated by the MM Shared Resource for a study investigating the role of ID2 in glioma biology, and now these mice are available for other researchers, here and outside Dartmouth, and can be combined with Cre-expressing mice to study the biology of ID2, a gene that that plays a role in multiple different cancers. In a second study involving genetically engineered mice, including a knock-in of a Cre-expression-regulated allele of constitutively active P110? of P13 kinase, the resulting model was the first reported rapidly developing murine breast tumor model that generates predominantly adenocarcinoma breast tumors, pathologically similar to human breast cancer. In contrast, other models are either very slow to develop or generate sarcomatoid breast tumors, which are rare in human breast cancer. MM?s menu of services constantly is evolving to respond to changing technologies and changing needs of new and established faculty at Dartmouth. Recently, we have been more involved providing mouse model experimentation services to support labs that either are not experienced with mouse experimentation or do not have sufficient lab personnel to support needed mouse studies, such as engineering faculty from Dartmouth?s Thayer School of Engineering, or research clinical faculty from Dartmouth-Hitchcock. Another new area of focus for MM is the use of CRISPR/Cas9 to make directly targeted genetic modifications in mouse zygotes with no intermediate tissue culture step with ES cells. Multiple mouse models have been made, and we continue to develop skills with this powerful technology.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA023108-42
Application #
10165514
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2020-12-01
Budget End
2021-11-30
Support Year
42
Fiscal Year
2021
Total Cost
Indirect Cost
Name
Dartmouth College
Department
Type
DUNS #
041027822
City
Hanover
State
NH
Country
United States
Zip Code
03755
Courtney, Andrea L; Rapuano, Kristina M; Sargent, James D et al. (2018) Reward System Activation in Response to Alcohol Advertisements Predicts College Drinking. J Stud Alcohol Drugs 79:29-38
Geller, Berta M; Frederick, Paul D; Knezevich, Stevan R et al. (2018) Pathologists' Use of Second Opinions in Interpretation of Melanocytic Cutaneous Lesions: Policies, Practices, and Perceptions. Dermatol Surg 44:177-185
Yeager, Mark P; Guyre, Cheryl A; Sites, Brian D et al. (2018) The Stress Hormone Cortisol Enhances Interferon-?-Mediated Proinflammatory Responses of Human Immune Cells. Anesth Analg 127:556-563
Rodriguez-Garcia, Marta; Fortier, Jared M; Barr, Fiona D et al. (2018) Isolation of Dendritic Cells from the Human Female Reproductive Tract for Phenotypical and Functional Studies. J Vis Exp :
Aschbrenner, Kelly A; Bobak, Carly; Schneider, Emily J et al. (2018) Egocentric social networks and smoking among adults with serious mental illness. Transl Behav Med 8:531-539
Tapp, Stephanie J; Martin, Brook I; Tosteson, Tor D et al. (2018) Understanding the value of minimally invasive procedures for the treatment of lumbar spinal stenosis: the case of interspinous spacer devices. Spine J 18:584-592
Kuklinski, Lawrence F; Yan, Shaofeng; Li, Zhongze et al. (2018) VISTA expression on tumor-infiltrating inflammatory cells in primary cutaneous melanoma correlates with poor disease-specific survival. Cancer Immunol Immunother 67:1113-1121
Shee, Kevin; Yang, Wei; Hinds, John W et al. (2018) Therapeutically targeting tumor microenvironment-mediated drug resistance in estrogen receptor-positive breast cancer. J Exp Med 215:895-910
Gareen, Ilana F; Black, William C; Tosteson, Tor D et al. (2018) Medical Care Costs Were Similar Across the Low-dose Computed Tomography and Chest X-Ray Arms of the National Lung Screening Trial Despite Different Rates of Significant Incidental Findings. Med Care 56:403-409
Miles, Randy; Wan, Fei; Onega, Tracy L et al. (2018) Underutilization of Supplemental Magnetic Resonance Imaging Screening Among Patients at High Breast Cancer Risk. J Womens Health (Larchmt) 27:748-754

Showing the most recent 10 out of 1911 publications