The Mayo SPORE in Brain Cancer comprises four investigator-initiated and led research projects, and four core resources constructed around a theme of malignant gliomas of adults. The Administrative Core provides a common management structure for the SPORE. This Core contributes to the overall efficiency of the SPORE and at the same time allows for economy of scale in its administrative and fiscal management. This in turn, frees investigators to concentrate on the science of the SPORE. The Administrative Core will support SPORE activities by providing: (1) Leadership, organizational support, and financial management for SPORE Investigators;(2) Coordination of monthly scientific meetings of SPORE investigators, and the ongoing scientific review of SPORE research projects and cores;(3) Information transfer to the scientific community via professional and public means;(4) Provision of common services for projects and cores such as administrative processing of reviews and funding statements, financial administration of grant funds, processing of IRB protocols and assurance of compliance with all NIH and Institutional grant regulations;(5) Coordination of the Internal and External Advisory Boards;(6) Oversight and management of the Developmental Research portfolio (Career Development Award; Developmental Research Award) of the SPORE;and, (7) Enhancement of communication between SPORE Investigators. The Administrative Core will foster Intra-SPORE, inter-SPORE, and intra-institutional collaborations;and, act as liaison with leadership of the other Brain SPOREs and the NCI SPORE Program.
Compared to other more common cancers malignant gliomas are responsible for a disproportionate amount of morbidity and mortality because of their disabling impact on cognition, memory, language, mobility, and adaptive skills. In addition to significant reduction in life expectancy each new case impacts the nation's public health since its morbidity represents on average twenty years of lost productivity. Whether the payer is public or private, diagnosis and treatment, including supportive care in the terminal stages of disease, extracts enormous health care expenditures.
|Oi, N; Yuan, J; Malakhova, M et al. (2015) Resveratrol induces apoptosis by directly targeting Ras-GTPase-activating protein SH3 domain-binding protein 1. Oncogene 34:2660-71|
|Choi, Jae Won; Schroeder, Mark A; Sarkaria, Jann N et al. (2014) Cyclophilin B supports Myc and mutant p53-dependent survival of glioblastoma multiforme cells. Cancer Res 74:484-96|
|Bradley, Barrie S; Loftus, Joseph C; Mielke, Clinton J et al. (2014) Differential expression of microRNAs as predictors of glioblastoma phenotypes. BMC Bioinformatics 15:21|
|Walsh, Kyle M; Codd, Veryan; Smirnov, Ivan V et al. (2014) Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk. Nat Genet 46:731-5|
|Bell, Michael P; Renner, Danielle N; Johnson, Aaron J et al. (2014) An elite controller of picornavirus infection targets an epitope that is resistant to immune escape. PLoS One 9:e94332|
|Catteau, Aurélie; Girardi, Hélène; Monville, Florence et al. (2014) A new sensitive PCR assay for one-step detection of 12 IDH1/2 mutations in glioma. Acta Neuropathol Commun 2:58|
|Johnson, Holly L; Jin, Fang; Pirko, Istvan et al. (2014) Theiler's murine encephalomyelitis virus as an experimental model system to study the mechanism of blood-brain barrier disruption. J Neurovirol 20:107-12|
|Gupta, Shiv K; Mladek, Ann C; Carlson, Brett L et al. (2014) Discordant in vitro and in vivo chemopotentiating effects of the PARP inhibitor veliparib in temozolomide-sensitive versus -resistant glioblastoma multiforme xenografts. Clin Cancer Res 20:3730-41|
|Assefnia, Shahin; Dakshanamurthy, Sivanesan; Guidry Auvil, Jaime M et al. (2014) Cadherin-11 in poor prognosis malignancies and rheumatoid arthritis: common target, common therapies. Oncotarget 5:1458-74|
|Wang, Enfeng; Zhang, Chunyang; Polavaram, Navatha et al. (2014) The role of factor inhibiting HIF (FIH-1) in inhibiting HIF-1 transcriptional activity in glioblastoma multiforme. PLoS One 9:e86102|
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