? Cytogenetics Shared Resource The Cytogenetic Shared Resource (CSR) is an SJCCC-managed Shared Resource with the overarching goal of providing Center members with access to high-quality, comprehensive cell-based genetic assays and associated expertise for cancer research. We accomplish this goal by collaborating with SJCCC members to determine project goals and develop and apply customized assays and analysis to advance member research. The CSR is directed by Marcus Valentine, who has more than 35 years of experience in cytogenetics and is a co-author of 90 peer-reviewed scientific articles. He is supported by 2 technologists, each of whom has more than 30 years of experience in the field. Examples of new assays developed in the current project period include assays for identifying the presence of numerous clinically actionable gene-fusion events in ALL (HMP, Roberts et al., NEJM, 2014) and assignment of hundreds of genes to specific epigenetic compartments within the retina (DBSTP, Aldiri et al., Neuron, 2017). The impact of the CSR on the cancer research of the Programs is evidenced by the high level of collaborative publications and key scientific contributions in high-impact journals such as Cancer Cell (n=5), Blood (n=3), and Nature Communications (n=4). During the current funding period, research from 53 publications from January 2013?December 2017 utilized the CSR, representing 15 (28%) interprogrammatic and 18 (34%) intraprogrammatic collaborations. These included publications from 4 of the 5 Programs: DBSTP (n=9), HMP (n=22), CBP (n=19), and NBTP (n=24). During the index year (FY2017), 85% of all investigators using the CSR were SJCCC members (22/26). Goals for the next period include continuing to develop and apply new assays to support the cancer research of SJCCC members in emerging areas such as epigenetics. In addition, to support the precision medicine goals of the SJCCC strategic plan, the CSR will work collaboratively with SJCCC members to develop and validate new assays as new gene rearrangements are discovered, and transfer these assays for implementation in patient diagnostics. Lastly, the CSR will monitor technical improvements in the field (eg., advanced microscopy) that may be appropriate for implementation in the CSR.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA021765-40
Application #
9632008
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
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
Sabin, N D; Cheung, Y T; Reddick, W E et al. (2018) The Impact of Persistent Leukoencephalopathy on Brain White Matter Microstructure in Long-Term Survivors of Acute Lymphoblastic Leukemia Treated with Chemotherapy Only. AJNR Am J Neuroradiol 39:1919-1925
Brinkman, Tara M; Recklitis, Christopher J; Michel, Gisela et al. (2018) Psychological Symptoms, Social Outcomes, Socioeconomic Attainment, and Health Behaviors Among Survivors of Childhood Cancer: Current State of the Literature. J Clin Oncol 36:2190-2197
Fuentes-Alabi, Soad; Bhakta, Nickhill; Vasquez, Roberto Franklin et al. (2018) The cost and cost-effectiveness of childhood cancer treatment in El Salvador, Central America: A report from the Childhood Cancer 2030 Network. Cancer 124:391-397
Bouchard, Jill J; Otero, Joel H; Scott, Daniel C et al. (2018) Cancer Mutations of the Tumor Suppressor SPOP Disrupt the Formation of Active, Phase-Separated Compartments. Mol Cell 72:19-36.e8
Flerlage, Jamie E; Metzger, Monika L; Bhakta, Nickhill (2018) The management of Hodgkin lymphoma in adolescents and young adults: burden of disease or burden of choice? Blood 132:376-384
Hijano, Diego R; Siefker, David T; Shrestha, Bishwas et al. (2018) Type I Interferon Potentiates IgA Immunity to Respiratory Syncytial Virus Infection During Infancy. Sci Rep 8:11034
Follis, Ariele Viacava; Llambi, Fabien; Kalkavan, Halime et al. (2018) Regulation of apoptosis by an intrinsically disordered region of Bcl-xL. Nat Chem Biol 14:458-465
Zheng, Daniel J; Krull, Kevin R; Chen, Yan et al. (2018) Long-term psychological and educational outcomes for survivors of neuroblastoma: A report from the Childhood Cancer Survivor Study. Cancer 124:3220-3230
Fatima, Soghra; Zhou, Sheng; Sorrentino, Brian P (2018) Marking of definitive HSC precursors in E7.5-E8.5 embryos using an Abcg2-CreER lineage-tracing mouse model. Exp Hematol 65:29-33

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