?Neurobiology and Brain Tumor Program Brain tumors are the leading cause of cancer-related death in children. Despite rapid advances in our understanding of disease biology, current treatment approaches are still lacking for some patients and lead to long-term, debilitating side effects in others. The goal of the Neurobiology and Brain Tumor Program (NBTP) is to improve survival and morbidity for children with brain tumors by developing effective, relatively non-toxic therapies through a better understanding of disease pathogenesis. The NBTP is an established multidisciplinary Program with a proven record in translating fundamental neuroscience and cancer biology discoveries into novel diagnostics and clinical trials. Our genome-wide studies of the major pediatric brain tumor types identified novel mutations, defined molecular subgroups, and opened new avenues of basic, translational, and clinical investigation. Exciting advances in the fields of molecular pathology, imaging, and radiation oncology provide additional promise for progress in treatment of these clinically formidable diseases. Drs. Suzanne Baker (laboratory lead), an expert in the molecular pathogenesis of brain tumors and Amar Gajjar (clinical lead), a nationally recognized leader in pediatric brain tumor therapeutics are responsible for the leadership of the Program. To facilitate collaboration and drive translation, the NBTP is organized into 3 working groups: Fundamental Neurobiology, Translational Research, and Brain Tumor Therapy. The NBTP has 16 Full Members and 3 Associate (junior mentored) Members, representing the Departments of Bone Marrow Transplantation and Cellular Therapy, Cell and Molecular Biology, Developmental Neurobiology, Genetics, Oncology, Pathology, Pediatric Medicine, Pharmaceutical Sciences, and Radiation Oncology. Program members have a total of $3.8M in annual peer-reviewed funding, including $2.6M in NCI funding, Research from the NBTP has resulted in 458 publications, of which 31.4% are intra-programmatic, 29.9% are inter- programmatic, and 77.5% are inter-institutional (with other NCI-designated Cancer Centers). In addition, during the funding period (2013-2017) the NBTP contributed 879 interventional enrollments of which 762 were therapeutic enrollments. During the current funding period, NBTP accomplishments led to a paradigm shift in the global understanding and treatment of commonly diagnosed pediatric brain tumors. Results from key NBTP studies included an unprecedented view of the somatic mutation landscape of several pediatric brain tumors; novel oncogenic drivers of DIPG and ependymoma; discovery of extensive heterogeneity within virtually all pediatric brain tumor histotypes; and new insights into the cellular origins and pathogenesis of pediatric brain tumors. NBTP members also translated our fundamental genetic discoveries into 4 early-phase clinical trials (SJHG12, SJPDGF, SJDAWN, SJATRT) and the precision medicine phase II trial SJMB12, a randomized, multicenter international study for newly diagnosed medulloblastoma. SJMB12 is the first trial in North America to assign strata based on molecular classification, with therapy translated from NBTP preclinical studies.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA021765-40
Application #
9632017
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2019-03-01
Budget End
2020-02-29
Support Year
40
Fiscal Year
2019
Total Cost
Indirect Cost
Name
St. Jude Children's Research Hospital
Department
Type
DUNS #
067717892
City
Memphis
State
TN
Country
United States
Zip Code
38105
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Broniscer, Alberto; Hwang, Scott N; Chamdine, Omar et al. (2018) Bithalamic gliomas may be molecularly distinct from their unilateral high-grade counterparts. Brain Pathol 28:112-120
Wogksch, Matthew D; Howell, Carrie R; Wilson, Carmen L et al. (2018) Physical fitness in survivors of childhood Hodgkin lymphoma: A report from the St. Jude Lifetime Cohort. Pediatr Blood Cancer :e27506
Nishii, Rina; Moriyama, Takaya; Janke, Laura J et al. (2018) Preclinical evaluation of NUDT15-guided thiopurine therapy and its effects on toxicity and antileukemic efficacy. Blood 131:2466-2474
Fernandez-Pineda, Israel; Davidoff, Andrew M; Lu, Lu et al. (2018) Impact of ovarian transposition before pelvic irradiation on ovarian function among long-term survivors of childhood Hodgkin lymphoma: A report from the St. Jude Lifetime Cohort Study. Pediatr Blood Cancer 65:e27232
Vanarotti, Murugendra; Evison, Benjamin J; Actis, Marcelo L et al. (2018) Small-molecules that bind to the ubiquitin-binding motif of REV1 inhibit REV1 interaction with K164-monoubiquitinated PCNA and suppress DNA damage tolerance. Bioorg Med Chem 26:2345-2353
Quinn, Melissa; Fannin, J T; Sciasci, Joseph et al. (2018) Pentamidine for Prophylaxis against Pneumocystis jirovecii Pneumonia in Pediatric Oncology Patients Receiving Immunosuppressive Chemotherapy. Antimicrob Agents Chemother 62:
Halalsheh, Hadeel; Kaste, Sue C; Navid, Fariba et al. (2018) The role of routine imaging in pediatric cutaneous melanoma. Pediatr Blood Cancer 65:e27412
Wang, Lu; Hiler, Daniel; Xu, Beisi et al. (2018) Retinal Cell Type DNA Methylation and Histone Modifications Predict Reprogramming Efficiency and Retinogenesis in 3D Organoid Cultures. Cell Rep 22:2601-2614
Wang, Xusheng; Jones, Drew R; Shaw, Timothy I et al. (2018) Target-Decoy-Based False Discovery Rate Estimation for Large-Scale Metabolite Identification. J Proteome Res 17:2328-2334

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