The Scientific Resources Core of this Program is a union of four shared resource components under the guidance of the Scientific Resources Core Leadership Committee. It provides the mechanisms to facilitate achievement of both the basic biologic/genetic and the clinical/translational themes of the Program. The 4 shared resource components are: 1.) Tissue and Pathology, 2.) Molecular Markers, 3.) Study Design and Data Analysis, and 4.) Bioinformatics. The Core Leadership Committee consists of the Directors of each of the core components, the Program Principal Investigator, and a medical oncologist. The key goals of the Core are: 1.) To a.) procure glioma specimens, b.) assure accurate diagnoses, c.) distribute high-quality specimens to Program Investigators, and d.) provide neuropathological expertise to individual project participants. 2.) To a.) evaluate the status of known and clinically relevant biomarkers identified by the project leaders in appropriate cohorts of patients, b.) perform other genetic analyses, and c.) assess novel markers identified by the projects during the grant period. 3.) To coordinate and monitor the acquisition and organization of appropriate clinical data corresponding to patient tumor specimens collected for the Program. 4.) To identify appropriate specimen cohorts for the conduct of clinical correlative studies in order to assure efficient and appropriate utilization of tissue resources. 5.) To help the project leaders develop, conduct, analyze, and publish well-designed clinical correlation studies, including extension and confirmation of exploratory marker studies. 6.) To perform clinical validation studies of the specific markers that are the primary targets of the project leaders and to interact with Cooperative Clinical Trials Groups to develop and perform collaborative validation studies of molecular markers in gliomas. And 7.) To manage key research data in an efficient, cost-effective and user-friendly manner that protects patient privacy and insures high-quality data. The structure and operations of each component are based on those developed for the Glioma Markers Network.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA085799-02
Application #
6606500
Study Section
Subcommittee E - Prevention &Control (NCI)
Project Start
2002-06-28
Project End
2003-05-31
Budget Start
Budget End
Support Year
2
Fiscal Year
2002
Total Cost
Indirect Cost
Name
Mayo Clinic, Rochester
Department
Type
DUNS #
City
Rochester
State
MN
Country
United States
Zip Code
55905
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Misra, Anjan; Pellarin, Malgorzata; Hu, Lily et al. (2006) Chromosome transfer experiments link regions on chromosome 7 to radiation resistance in human glioblastoma multiforme. Genes Chromosomes Cancer 45:20-30
Nigro, Janice M; Misra, Anjan; Zhang, Li et al. (2005) Integrated array-comparative genomic hybridization and expression array profiles identify clinically relevant molecular subtypes of glioblastoma. Cancer Res 65:1678-86
Misra, Anjan; Pellarin, Malgorzata; Nigro, Janice et al. (2005) Array comparative genomic hybridization identifies genetic subgroups in grade 4 human astrocytoma. Clin Cancer Res 11:2907-18
Law, Mark E; Templeton, Kristen L; Kitange, Gaspar et al. (2005) Molecular cytogenetic analysis of chromosomes 1 and 19 in glioma cell lines. Cancer Genet Cytogenet 160:1-14

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