The Program includes 27 members from 8 basic and clinical departments within Duke University. Total funding for program members is $21,313,013, of which $13,716,487 is from peer- reviewed sources. A cancer focus is illustrated by $9,448,240 or 68.9% of funding from the NCI, the American Cancer Society or the Department of Defense. From 2004-2008, program members published 628 papers in peer-reviewed journals cited in PubMed. Of these publications, 6% are the result of intra-programmatic collaborations and 33% due to inter-programmatic collaborations.The scientific goals of the Program are to 1) conduct basic, translational and clinical research to elucidate mechanisms of action and of resistance of cancer therapies that target cellular and molecular abnormalities and cell signaling pathways; 2) identify biomarkers, pharmacokinetic/pharmacodynamic endpoints, and molecular and functional imaging parameters that correlate with the anti-tumor activity of cancer therapies and 3) develop innovative methods and strategies for optimized delivery of cancer therapeutics, specifically, small molecules, gene therapy and biologies, 4) design and conduct innovative clinical trials of novel and current therapies that incorporate knowledge of of drug action and resistance, biomarkers, endpoints of response, and advances in pharmacogenomics and pharmacogenetics, and 5) conduct eariy phase discovery, evaluation and optimization of small molecule therapeutics directed against novel therapeutic targets and pathways deregulated in cancer. The organizational goals of the Program are to provide an infrastructure to facilitate the discovery and evaluation of new cancer therapies, enhance pursuit of individual research programs of program members, and facilitate intra- and inter-programmatic collaborative research activities in the area of cancer therapeutics. This will include the organization of retreats, seminar series and related program activities to facilitate interaction and exchange of ideas and information between programs and program members. A major programmatic goal is to promote and enhance training of graduate students, post-doctoral fellows and physician-scientists in basic, translational and clinical sciences relevant to cancer therapeutics. The structure of the program represents a continuum of research activities from the bench to the clinic that provides an ideal environment and opportunity to conduct translational research in an iterative process involving testing findings from the laboratory into hypothesis-driven mechanistic clinical trials, that can generate new questions to be addressed in the laboratory, thereby constantly refining and honing hypotheses that can lead to more effective therapies for cancer.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA014236-38
Application #
8379537
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2012-01-01
Budget End
2012-12-31
Support Year
38
Fiscal Year
2012
Total Cost
$36,343
Indirect Cost
Name
Duke University
Department
Type
DUNS #
044387793
City
Durham
State
NC
Country
United States
Zip Code
27705
Feng, Yun; Wang, Yanru; Liu, Hongliang et al. (2018) Novel genetic variants in the P38MAPK pathway gene ZAK and susceptibility to lung cancer. Mol Carcinog 57:216-224
Naqvi, Ibtehaj; Gunaratne, Ruwan; McDade, Jessica E et al. (2018) Polymer-Mediated Inhibition of Pro-invasive Nucleic Acid DAMPs and Microvesicles Limits Pancreatic Cancer Metastasis. Mol Ther 26:1020-1031
Wen, Juyi; Liu, Hongliang; Wang, Lili et al. (2018) Potentially Functional Variants of ATG16L2 Predict Radiation Pneumonitis and Outcomes in Patients with Non-Small Cell Lung Cancer after Definitive Radiotherapy. J Thorac Oncol 13:660-675
Li, Bo; Wang, Yanru; Xu, Yinghui et al. (2018) Genetic variants in RORA and DNMT1 associated with cutaneous melanoma survival. Int J Cancer 142:2303-2312
Gearhart-Serna, Larisa M; Jayasundara, Nishad; Tacam Jr, Moises et al. (2018) Assessing Cancer Risk Associated with Aquatic Polycyclic Aromatic Hydrocarbon Pollution Reveals Dietary Routes of Exposure and Vulnerable Populations. J Environ Public Health 2018:5610462
Bakthavatsalam, Subha; Sleeper, Mark L; Dharani, Azim et al. (2018) Leveraging ?-Glutamyl Transferase To Direct Cytotoxicity of Copper Dithiocarbamates against Prostate Cancer Cells. Angew Chem Int Ed Engl 57:12780-12784
Dai, Ziwei; Mentch, Samantha J; Gao, Xia et al. (2018) Methionine metabolism influences genomic architecture and gene expression through H3K4me3 peak width. Nat Commun 9:1955
Powell Gray, Bethany; Kelly, Linsley; Ahrens, Douglas P et al. (2018) Tunable cytotoxic aptamer-drug conjugates for the treatment of prostate cancer. Proc Natl Acad Sci U S A 115:4761-4766
Abdi, Khadar; Lai, Chun-Hsiang; Paez-Gonzalez, Patricia et al. (2018) Uncovering inherent cellular plasticity of multiciliated ependyma leading to ventricular wall transformation and hydrocephalus. Nat Commun 9:1655
Hudson, Kathryn E; Rizzieri, David; Thomas, Samantha M et al. (2018) Dose-intense chemoimmunotherapy plus radioimmunotherapy in high-risk diffuse large B-cell lymphoma and mantle cell lymphoma: a phase II study. Br J Haematol :

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