? FLOW CYTOMETRY SHARED RESOURCE The Flow Cytometry (FC) shared resource supports Duke Cancer Institute (DCI) investigators with sorting and/or analyzing populations of cells based on expression of surface proteins or fluorescent reporters, and performing batch or single-cell sorting. Flow cytometry allows investigators to analyze parameters such as cell death, cell cycle, cell signaling, and cytokine production as a function of cellular state or stimulation.
Our Specific Aims are: 1) Maintain state-of-the-art cell sorters and cell analyzers in a cost-effective manner to meet DCI research needs; 2) Provide expertise in assay development, troubleshooting, and data analysis; and 3) Train DCI members to use cytometers independently. The resource maintains four analyzers, four cell sorters, and one image cytometer; analyzers and the image cytometer are available for self-use, 24 hrs per day and 365 days per year. FC staff is actively engaged in DCI member research projects, working closely with clients to fine tune their individual experiments and develop strategies for best outcomes in real time. Based on our extensive experience, we are able to recommend assays, to help develop and troubleshoot new protocols, and participate in data analysis. The FC?s experienced staff performs cell sorting, cell analysis, and post-acquisition data handling. These services would otherwise be unaffordable to investigators, given the costs, time, and training required to purchase, use, and maintain the necessary equipment. Flow cytometry services are not outsourced easily, given the fragile and time-sensitive nature of the cell preparations and the experimental protocols. An important and continuing mission of the FC resource is educating clients to ensure that all DCI members use the services and technology that best support their research goals. We provide ongoing training in the use of cytometers and associated software, and maintain a library to disseminate technical information to users. DCI members receive priority services, and FC operates on a charge-back basis with different rates for staff-run or self-run work. DCI member laboratories get added value in the form of a 25% discount on usage fees compared to non-DCI member labs. In 2018, the FC provided services to 190 investigators, 61% of whom were DCI members who accounted for 78% of total usage and represented all 8 DCI Research Programs. Use of the shared resource by DCI Members, contributed to 320 publications over the project period, 104 of which were in high impact journals (Impact Factor>9).

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA014236-46
Application #
9853592
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
Wu, Mengxi; Huang, Po-Hsun; Zhang, Rui et al. (2018) Circulating Tumor Cell Phenotyping via High-Throughput Acoustic Separation. Small 14:e1801131
Vlahovic, Gordana; Meadows, Kellen L; Hatch, Ace J et al. (2018) A Phase I Trial of the IGF-1R Antibody Ganitumab (AMG 479) in Combination with Everolimus (RAD001) and Panitumumab in Patients with Advanced Cancer. Oncologist 23:782-790
Xu, Yinghui; Liu, Hongliang; Liu, Shun et al. (2018) Genetic variant of IRAK2 in the toll-like receptor signaling pathway and survival of non-small cell lung cancer. Int J Cancer 143:2400-2408
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

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