The University of Colorado Anschutz Medical Campus MD/PhD Program was established in 1983 and obtained NIH/MSTP funding in 1993. This is the 5th competitive review, with essentially a fixed number of slots (15-16) for the past 20 years. The goal of this Program is to train a diverse cadre of dual-degree students to become outstanding physician-scientists and future leaders in biomedical research. To accomplish this goal, we select students from an increasing national applicant pool, seeking out those candidates whose record of research, academic, and leadership achievements are exemplary. Our pool size has increased significantly, from 154 in 2007 to 397 in 2016. We matriculate ~11 students annually, with plans to increase to 15/year in the next funding cycle. Our current roster of 75 students (45% female; 12% URM; 8% disability; 15% disadvantaged; and 9% 1st generation college) come from across the nation, from elite universities, and with ~30 months of prior research experience and ~60% with prior publication(s). The selected MSTP students enter a flexible, yet highly rigorous training program that interdigitates graduate and medical school courses in the first two years, by substituting graduate for medical school courses, and vice-versa, followed by one required MSIII clinical clerkship, with an option for a second. They then complete ~4 years of thesis work, followed by 16-24 months of MSIII/IV clinical work. An MSTP-specific Molecules to Medicine course, Seminar Series, and a Longitudinal Clinical experience during the thesis years have been specifically developed for our students. For thesis research, students choose from 193 total MSTP faculty in 15 graduate training programs, with the 100 faculty selected for this submission having $590K grant income/yr. MSTPs train at three sites: the new Anschutz Medical Campus, National Jewish Health, and the University of Colorado-Boulder, which have a combined grant income of ~$1B. To enhance the success of our MSTP students, we provide career guidance beyond the PhD thesis years, and we work diligently to place our graduates in elite residencies and fellowships. Since 1983, 214 students have matriculated, 28 are URMs, 19 left the program, 124 graduated with both degrees in 8 years, and 85 completed all of their training with 50 pursuing research in academics, the NIH/CDC, or industry, 32 in private practice, and 3 lost to follow-up. AMC has provided increasing support to MSTP, totaling $12.6M during the last funding cycle. The new Campus provides state-of-the-art education, research and clinical facilities, and enjoys significant momentum with ~$480M in grants, $450M in philanthropy and ~$100M in clinical income to fund research and programs. The SOM Dean John Reilly has funded 5 new basic/clinical collaborative Translational Research initiatives that will recruit ~15 new faculty. In sum, the continuous improvement of the Program, applicant pool, recruited students, training faculty and plan, student outcomes, institutional support, and research funding and environment justifies our request for 20 slots/year.

Public Health Relevance

Clinical disorders, such as Alzheimers, auto-immunity, diabetes, cancer, hypertension, obesity and genetic diseases result in significant human suffering, and unnecessary morbidity and mortality. To mitigate the negative impact of these diseases, it is critical to train a cadre of physician-scientists who can identify the most important questions in medicine, and then apply the most rigorous scientific investigation tools to discover disease mechanism, novel treatments, and optimal prevention strategies. Trainees supported by this grant will become the future biomedical physician-scientists who will work towards increasing our understanding of fundamental pathogenesis of disease and cutting-edge approaches to treat patients.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Institutional National Research Service Award (T32)
Project #
5T32GM008497-27
Application #
9736555
Study Section
NIGMS Initial Review Group (TWD)
Program Officer
Gindhart, Joseph G
Project Start
1993-07-01
Project End
2023-06-30
Budget Start
2019-07-01
Budget End
2020-06-30
Support Year
27
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Colorado Denver
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
041096314
City
Aurora
State
CO
Country
United States
Zip Code
80045
Garcia, Tamara B; Fosmire, Susan P; Porter, Christopher C (2018) Increased activity of both CDK1 and CDK2 is necessary for the combinatorial activity of WEE1 inhibition and cytarabine. Leuk Res 64:30-33
Pei, Shanshan; Minhajuddin, Mohammad; Adane, Biniam et al. (2018) AMPK/FIS1-Mediated Mitophagy Is Required for Self-Renewal of Human AML Stem Cells. Cell Stem Cell 23:86-100.e6
Chun, Carlene; Zheng, Leon; Colgan, Sean P (2017) Tissue metabolism and host-microbial interactions in the intestinal mucosa. Free Radic Biol Med 105:86-92
Sinnen, Brooke L; Bowen, Aaron B; Forte, Jeffrey S et al. (2017) Optogenetic Control of Synaptic Composition and Function. Neuron 93:646-660.e5
Dillon, Stephanie M; Kibbie, Jon; Lee, Eric J et al. (2017) Low abundance of colonic butyrate-producing bacteria in HIV infection is associated with microbial translocation and immune activation. AIDS 31:511-521
Estin, Miriam L; Thompson, Scott B; Traxinger, Brianna et al. (2017) Ena/VASP proteins regulate activated T-cell trafficking by promoting diapedesis during transendothelial migration. Proc Natl Acad Sci U S A 114:E2901-E2910
Yang, Yimu; Haeger, Sarah M; Suflita, Matthew A et al. (2017) Fibroblast Growth Factor Signaling Mediates Pulmonary Endothelial Glycocalyx Reconstitution. Am J Respir Cell Mol Biol 56:727-737
Keysar, Stephen B; Le, Phuong N; Miller, Bettina et al. (2017) Regulation of Head and Neck Squamous Cancer Stem Cells by PI3K and SOX2. J Natl Cancer Inst 109:
White, Jason T; Cross, Eric W; Kedl, Ross M (2017) Antigen-inexperienced memory CD8+ T cells: where they come from and why we need them. Nat Rev Immunol 17:391-400
Scarborough, Hannah A; Helfrich, Barbara A; Casás-Selves, Matias et al. (2017) AZ1366: An Inhibitor of Tankyrase and the Canonical Wnt Pathway that Limits the Persistence of Non-Small Cell Lung Cancer Cells Following EGFR Inhibition. Clin Cancer Res 23:1531-1541

Showing the most recent 10 out of 159 publications