? 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 #
5P30CA021765-41
Application #
9883741
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2020-03-01
Budget End
2021-02-28
Support Year
41
Fiscal Year
2020
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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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
Stewart, Elizabeth; McEvoy, Justina; Wang, Hong et al. (2018) Identification of Therapeutic Targets in Rhabdomyosarcoma through Integrated Genomic, Epigenomic, and Proteomic Analyses. Cancer Cell 34:411-426.e19
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
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
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:
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

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