Traditional graduate and medical programs provide researchers with program-specific background, training, and scientific expertise, but they fail to provide students with the breadth of knowledge and interdisciplinary understanding required to successfully translate basic science discoveries into clinical outcomes. Translational investigators trained within these programs have historically overcome this by engaging in """"""""team science"""""""" to assemble the scientific expertise needed for a translational project. Inspired by changing trends in the conduct of biomedical science research, and in efforts to encourage young faculty to participate in translational team projects, the NIH revised its criteria for faculty tenure to acknowledge the importance and contributions of team science in 2006. Despite this adaptation, many individual institutions have been slow to adopt these policies and thus young faculty are often conflicted due to contradictions between the metrics of success in team science and those by which they are evaluated in the traditional academic tenure career path. To complicate the matter, recent U.S. labor statistics indicate that while the number of PhDs granted over the past 10 years has doubled in the biomedical fields, the number of tenure-based faculty positions has remained constant. This concerning trend is further exacerbated by recent layoffs in industry-based drug discovery departments and decreases in federal and state funding. Inevitably, the simple laws of supply and demand are making it more competitive (and difficult) to secure and maintain academic tenure positions. The culmination of these contradictions and pressures is negatively impacting translational research in the academic environment. The DTMI-CTHD believes that the broad spectrum training delineated herein would better prepare translational scientists to compete in the current market, foster successful academic research careers, and ultimately allow participants to facilitate translational research and contribute to the translational research community in a variety of capacities.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Specialized Center--Cooperative Agreements (U54)
Project #
1U54HL112307-01
Application #
8391975
Study Section
Special Emphasis Panel (ZHL1-CSR-C (F1))
Project Start
Project End
Budget Start
2012-05-15
Budget End
2013-04-30
Support Year
1
Fiscal Year
2012
Total Cost
$315,132
Indirect Cost
$102,384
Name
Duke University
Department
Type
DUNS #
044387793
City
Durham
State
NC
Country
United States
Zip Code
27705
Fager, A M; Machlus, K R; Ezban, M et al. (2018) Human platelets express endothelial protein C receptor, which can be utilized to enhance localization of factor VIIa activity. J Thromb Haemost 16:1817-1829
Nimjee, Shahid M; White, Rebekah R; Becker, Richard C et al. (2017) Aptamers as Therapeutics. Annu Rev Pharmacol Toxicol 57:61-79
Lee, Jaewoo; Lee, Youngju; Xu, Li et al. (2017) Differential Induction of Immunogenic Cell Death and Interferon Expression in Cancer Cells by Structured ssRNAs. Mol Ther 25:1295-1305
Lee, Jaewoo; Jackman, Jennifer G; Kwun, Jean et al. (2017) Nucleic acid scavenging microfiber mesh inhibits trauma-induced inflammation and thrombosis. Biomaterials 120:94-102
Hoffman, Maureane; Monroe, Dougald M (2017) Impact of Non-Vitamin K Antagonist Oral Anticoagulants From a Basic Science Perspective. Arterioscler Thromb Vasc Biol 37:1812-1818
Lee, Youngju; Urban, Johannes H; Xu, Li et al. (2016) 2'Fluoro Modification Differentially Modulates the Ability of RNAs to Activate Pattern Recognition Receptors. Nucleic Acid Ther 26:173-82
Soule, Erin E; Bompiani, Kristin M; Woodruff, Rebecca S et al. (2016) Targeting Two Coagulation Cascade Proteases with a Bivalent Aptamer Yields a Potent and Antidote-Controllable Anticoagulant. Nucleic Acid Ther 26:1-9
Ganson, Nancy J; Povsic, Thomas J; Sullenger, Bruce A et al. (2016) Pre-existing anti-polyethylene glycol antibody linked to first-exposure allergic reactions to pegnivacogin, a PEGylated RNA aptamer. J Allergy Clin Immunol 137:1610-1613.e7
Woodruff, Rebecca S; Sullenger, Bruce A (2015) Modulation of the Coagulation Cascade Using Aptamers. Arterioscler Thromb Vasc Biol 35:2083-91
Bompiani, Kristin M; Lohrmann, Jens L; Pitoc, George A et al. (2014) Probing the coagulation pathway with aptamers identifies combinations that synergistically inhibit blood clot formation. Chem Biol 21:935-44