? 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
Gibson, Todd M; Li, Chenghong; Armstrong, Gregory T et al. (2018) Perceptions of future health and cancer risk in adult survivors of childhood cancer: A report from the Childhood Cancer Survivor Study. Cancer 124:3436-3444
Yang, Kai; Blanco, Daniel Bastardo; Chen, Xiang et al. (2018) Metabolic signaling directs the reciprocal lineage decisions of ?? and ?? T cells. Sci Immunol 3:
Ferrolino, Mylene C; Mitrea, Diana M; Michael, J Robert et al. (2018) Compositional adaptability in NPM1-SURF6 scaffolding networks enabled by dynamic switching of phase separation mechanisms. Nat Commun 9:5064
Bjornard, Kari L; Gilchrist, Laura S; Inaba, Hiroto et al. (2018) Peripheral neuropathy in children and adolescents treated for cancer. Lancet Child Adolesc Health 2:744-754
Luo, Yi; Shao, Lijian; Chang, Jianhui et al. (2018) M1 and M2 macrophages differentially regulate hematopoietic stem cell self-renewal and ex vivo expansion. Blood Adv 2:859-870
Peterson, Rachel K; Ashford, Jason M; Scott, Sarah M et al. (2018) Predicting parental distress among children newly diagnosed with craniopharyngioma. Pediatr Blood Cancer 65:e27287
Kumar, Rahul; Liu, Anthony P Y; Orr, Brent A et al. (2018) Advances in the classification of pediatric brain tumors through DNA methylation profiling: From research tool to frontline diagnostic. Cancer 124:4168-4180
Rusch, Michael; Nakitandwe, Joy; Shurtleff, Sheila et al. (2018) Clinical cancer genomic profiling by three-platform sequencing of whole genome, whole exome and transcriptome. Nat Commun 9:3962
Kurmasheva, Raushan T; Kurmashev, Dias; Reynolds, C Patrick et al. (2018) Initial testing (stage 1) of M6620 (formerly VX-970), a novel ATR inhibitor, alone and combined with cisplatin and melphalan, by the Pediatric Preclinical Testing Program. Pediatr Blood Cancer 65:
Chamdine, Omar; Elhawary, Ghada Ahmad Saad; Alfaar, Ahmad Samir et al. (2018) The incidence of brainstem primitive neuroectodermal tumors of childhood based on SEER data. Childs Nerv Syst 34:431-439

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