The Cell Analysis Core is designed to provide support to the clinical and basic projects by centralizing common procedures. These include sample acquisition, characterization, and distribution and banking; cell sorting; analytical flow cytometry; and histology and immunohistochemistry. By centralizing sample acquisition and storage we will be able to track samples and maintain records of expected data for each sample used, thus increasing the efficiency of data collection. A priority list for sample distribution will be established by the Core Oversight Committee and updated periodically to accommodate requirements of the different projects in terms of cell numbers, sample type, patient characteristics, and other ielevant criteria. This mechanism will greatly enhance the efficiency of sample utilization by the different projects. A centralized histology and immunohistochemistry service will avoid the need to establish the procedures in each investigator's laboratory, providing for uniformity of procedures and efficient use of materials. The flow cytometry and cell sorting service offered will provide state-of-the-art flow cytometry and cell sorting support to the projects in this program application. Able individuals experienced in the various procedures will supervise the different functions of the core.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
2P01CA055819-10
Application #
6997948
Study Section
Subcommittee G - Education (NCI)
Project Start
2004-08-16
Project End
2009-06-30
Budget Start
2004-08-16
Budget End
2005-06-30
Support Year
10
Fiscal Year
2004
Total Cost
$413,057
Indirect Cost
Name
University of Arkansas for Medical Sciences
Department
Type
DUNS #
122452563
City
Little Rock
State
AR
Country
United States
Zip Code
72205
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Went, Molly; Sud, Amit; Försti, Asta et al. (2018) Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma. Nat Commun 9:3707
Mehdi, Syed J; Johnson, Sarah K; Epstein, Joshua et al. (2018) Mesenchymal stem cells gene signature in high-risk myeloma bone marrow linked to suppression of distinct IGFBP2-expressing small adipocytes. Br J Haematol :
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Rasche, Leo; Angtuaco, Edgardo; McDonald, James E et al. (2017) Low expression of hexokinase-2 is associated with false-negative FDG-positron emission tomography in multiple myeloma. Blood 130:30-34
Mikulasova, Aneta; Wardell, Christopher P; Murison, Alexander et al. (2017) The spectrum of somatic mutations in monoclonal gammopathy of undetermined significance indicates a less complex genomic landscape than that in multiple myeloma. Haematologica 102:1617-1625

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