The Program in Nucleic Acid Biology focuses on mechanisms underlying DNA replication and mutagenesis as well as on the post-transcriptional regulation of gene expression by processes such as alternative splicing and microRNA function. The Program includes basic researchers interested in cell transformation and cancer who focus their work on a wide range of interrelated topics, including human genetics, DNA replication and repair, mRNA transcription and processing and gene regulation by endogenous or introduced non-coding RNAs. Program members share a common interest in the role of protein:nucleic acid interactions in regulating gene expression and cell growth. Although there is a significant interest in using prokaryotic model systems, the primary focus is on eukaryotic cells. Members interact through regularly scheduled research presentations, such as those sponsored by the Duke Center for RNA Biology, and through a wide range of relevant seminar presentations. Collaborations between members of the program, and particularly with other Cancer Center members, are numerous and productive. A new initiative relates to efforts to use RNA interference (RNAi) to study the role of specific viral and cellular gene products in the regulation of cell growth and transformation as well as to study the potentially critical role of the large endogenous family of non-coding RNA, termed microRNAs, in these processes. Co-leaders of the Program are Bryan R. Cullen, James B. Duke Professor of Molecular Genetics and Microbiology, and Mariano Garcia- Blanco, Professor of Molecular Genetics and Microbiology. The Program includes 21 members from 7 basic and clinical departments within Duke University. Total funding for program members is $7,599,091, of which $7,177,023 is from peer-reviewed sources. A cancer focus is illustrated by $790,117 or 11 % of funding from the NCI, the American Cancer Society or the Department of Defense. From 2004-2008, program members published 290 papers in peer-reviewed journals cited in PubMed. Of these publications, 2.4% are the result of intra-programmatic collaborations and 9.0% due to inter-programmatic collaborations. The program serves to focus the research of this very strong group of scientists on different aspects of the molecular genetics of cancer.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA014236-38
Application #
8379525
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
$18,171
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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