? OPTICAL MOLECULAR IMAGING AND ANALYSIS SHARED RESOURCE The Optical Molecular Imaging and Analysis (OMIA) shared resource provides in vivo optical imaging and spectroscopy ranging from whole animal fluorescence and bioluminescence to functional intravital microscopy. OMIA services can be broken down broadly according to the following categories: 1) optical imaging, 2) window chamber surgery training and support, 3) user training in techniques, and 4) scientific guidance on experimental design, data analysis and interpretation. Within optical imaging, two primary technological approaches are in vivo whole animal bioluminescence and fluorescence imaging. These are achieved using a set of commercial imaging devices, namely the IVIS Lumina and Kinetic, as well as FMT2500LX fluorescence tomography system (all from PerkinElmer). A third major technological approach within optical imaging is intravital microscopy. This approach is facilitated through resources developed over many years in the laboratories of the shared resource co-directors. The available resources include a surgical facility and the supplies needed for performing surgeries, as well as microscopes suitable for intravital functional imaging. Together, these three optical imaging capabilities, plus the other expertise, training, and services of OMIA, provide a unique resource for DCI members to study cancer therapeutics and tumor biology. This is a vital shared resource that, in 2018, provided services to 38 investigators, 71% of whom were DCI members, accounting for 74% of total usage, from all 8 DCI Research Programs. DCI members benefit in particular due to the availability of cost offsets that are proportional to the DCI contribution (typically 10-30% based on the service), as well as a wide range of cancer models, which account for the majority of the utilization of these services. The impact of this facility on DCI members is best highlighted by the fact that this shared resource contributed to 83 publications over the project period, 15 of which were in high impact journals (Impact Factor >9), demonstrating the value of services offered by the resource.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA014236-46
Application #
9853597
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2020-01-01
Budget End
2020-12-31
Support Year
46
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Duke University
Department
Type
DUNS #
044387793
City
Durham
State
NC
Country
United States
Zip Code
27705
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 :
Fayanju, Oluwadamilola M; Park, Ko Un; Lucci, Anthony (2018) Molecular Genomic Testing for Breast Cancer: Utility for Surgeons. Ann Surg Oncol 25:512-519
Porter, Laura S; Fish, Laura; Steinhauser, Karen (2018) Themes Addressed by Couples With Advanced Cancer During a Communication Skills Training Intervention. J Pain Symptom Manage 56:252-258
Káradóttir, Ragnhildur T; Kuo, Chay T (2018) Neuronal Activity-Dependent Control of Postnatal Neurogenesis and Gliogenesis. Annu Rev Neurosci 41:139-161
Han, Peng; Liu, Hongliang; Shi, Qiong et al. (2018) Associations between expression levels of nucleotide excision repair proteins in lymphoblastoid cells and risk of squamous cell carcinoma of the head and neck. Mol Carcinog 57:784-793
Xu, Yinghui; Wang, Yanru; Liu, Hongliang et al. (2018) Genetic variants in the metzincin metallopeptidase family genes predict melanoma survival. Mol Carcinog 57:22-31
Abdi, Khadar; Kuo, Chay T (2018) Laminating the mammalian cortex during development: cell polarity protein function and Hippo signaling. Genes Dev 32:740-741
Lu, Min; Sanderson, Sydney M; Zessin, Amelia et al. (2018) Exercise inhibits tumor growth and central carbon metabolism in patient-derived xenograft models of colorectal cancer. Cancer Metab 6:14
Qian, Danwen; Liu, Hongliang; Wang, Xiaomeng et al. (2018) Potentially functional genetic variants in the complement-related immunity gene-set are associated with non-small cell lung cancer survival. Int J Cancer :

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