?Cell and Tissue Imaging Shared Resource The primary goal of the Cell and Tissue Imaging Shared Resource (CTISR) is to make state-of-the-art technology and analysis tools for imaging cells and tissues available to SJCCC investigators and trainees. The CTISR consists of 2 divisions: Light Microscopy, led by Dr. Victoria Frohlich, and Electron Microscopy, led by Sharon Frase. Together, Frohlich and Frase have more than 90 years of experience in scientific imaging. The CTISR is further staffed by 8 experienced imaging scientists who assist with acquisition, analysis, quantification, presentation, and publication of imaging data. The CTISR staff collaborates with SJCCC members prior to beginning a project to provide guidance on experimental design, appropriate imaging modalities, sample preparation, and data-analysis options. The degree of direct staff involvement in specimen preparation, imaging, and analysis is determined. The CTISR also provides user training when applicable. During the reporting period (FY2017), CTISR-LM conducted 60 consultations with 40 SJCCC labs and trained 95 new instrument users. Selected accomplishments in the current reporting period include a collaboration with Drs. Tanja Mittag (CBP), Richard Kriwacki (CBP), and J. Paul Taylor (NBTP) to visualize and characterize the role of liquid?liquid phase transition in the formation and maintenance of membraneless organelles. This work is now being expanded in an SJCCC-funded inter-center Collaborative as described in the Strategic Plan section of the Director's Overview. Additionally, CTISR staff assisted Dr. Charles Mullighan (HMP Co-Leader) to document, by confocal and in situ multiphoton imaging, the perturbations and stem cell-like phenotype caused by mutated IKZF1, a hallmark of high-risk acute lymphoblastic leukemia (ALL) and to detect the reversal by treatment with retinoids. As a result, clinical evaluation of retinoids for IKZF1-altered Philadelphia chromosome-positive ALL is being pursued (Churchman et al., Cancer Cell, 2015). During the current project period, CTISR contributed to 159 publications authored by SJCCC members. Of these, 40 (25%) were interprogrammatic and 34 (21%) were intraprogrammatic. CTISR staff were co-authors of 24 (15%) of the publications, signifying the value of their expertise to the research presented. CTISR resources contributed to 70 publications in high-impact journals (impact factor >10) such as Cell, Nature, and Nature Genetics. Over the next five years, the CTISR plans to continuously expand and evolve services?including education and training programs?and technologies such as Lattice Lightsheet and virtual reality visualization, enabling SJCCC members to effectively pursue emerging directions in cancer research. CTISR staff will continue to educate SJCCC members on available methods to use correlative microscopy (CLEM) approaches to enhance cancer research. By leveraging and incorporating high-performance computing resources, the CTISR will augment statistical and analytical tools and assist SJCCC members in applying these tools to their research.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA021765-41
Application #
9883739
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
Sadighi, Zsila S; Curtis, Elizabeth; Zabrowksi, Jennifer et al. (2018) Neurologic impairments from pediatric low-grade glioma by tumor location and timing of diagnosis. Pediatr Blood Cancer 65:e27063
Wierdl, Monika; Tsurkan, Lyudmila; Chi, Liying et al. (2018) Targeting ALK in pediatric RMS does not induce antitumor activity in vivo. Cancer Chemother Pharmacol 82:251-263
Penkert, Rhiannon R; Hurwitz, Julia L; Thomas, Paul et al. (2018) Inflammatory molecule reduction with hydroxyurea therapy in children with sickle cell anemia. Haematologica 103:e50-e54
Turner, Benjamin L; Brenes-Arguedas, Tania; Condit, Richard (2018) Pervasive phosphorus limitation of tree species but not communities in tropical forests. Nature 555:367-370
Buchman, Cameron D; Chai, Sergio C; Chen, Taosheng (2018) A current structural perspective on PXR and CAR in drug metabolism. Expert Opin Drug Metab Toxicol 14:635-647
Gibbs, E B; Kriwacki, R W (2018) Direct detection of carbon and nitrogen nuclei for high-resolution analysis of intrinsically disordered proteins using NMR spectroscopy. Methods 138-139:39-46
Pui, Ching-Hon; Liu, Yiwei; Relling, Mary V (2018) How to solve the problem of hypersensitivity to asparaginase? Pediatr Blood Cancer 65:
Mukkada, Sheena; Smith, Cristel Kate; Aguilar, Delta et al. (2018) Evaluation of a fever-management algorithm in a pediatric cancer center in a low-resource setting. Pediatr Blood Cancer 65:
Zhong, Bo; Maharaj, Anil; Davis, Abigail et al. (2018) Development and validation of a sensitive LC MS/MS method for the measurement of the checkpoint kinase 1 inhibitor prexasertib and its application in a cerebral microdialysis study. J Pharm Biomed Anal 156:97-103
van Oosterwijk, Jolieke G; Buelow, Daelynn R; Drenberg, Christina D et al. (2018) Hypoxia-induced upregulation of BMX kinase mediates therapeutic resistance in acute myeloid leukemia. J Clin Invest 128:369-380

Showing the most recent 10 out of 6764 publications