The mission of the Drug Development Core (DDC) is to make state-of-the-art drug development accessible and affordable to UWCCC members. Development of innovative therapies is a priority area of research in the UWCCC Strategic Plan, and drug development requires specialized expertise in synthetic, computational, and analytical chemistry. The overarching scientific discipline in the DDC is medicinal chemistry in its broadest sense. DDC offers compound discovery by high throughput screening (HTS); computational chemistry for in silico virtual screening and modeling; chemical informatics to identify and prioritize compounds; chemical synthesis of potent, selective, and pharmacologically viable compounds; and analytical chemistry to support UWCCC clinical trials with pharmacokinetic (PK) and pharmacodynamic (PD) assays.
Aim 1 is to advance UWCCC member drug development research by providing broad medicinal chemistry expertise and infrastructure encompassing discovery, synthetic chemistry, computational chemistry, analytical chemistry, and pharmacology of chemoprevention and anticancer agents. DDC staff advise UWCCC members in all aspects of experimental design and data interpretation. The highly-skilled and experienced staff are experts in the use of state-of-the-art equipment for microwave-facilitated organic synthesis, analytical and preparative HPLC, mass spectrometry, combi-flash chromatography, tip-less and tip-based liquid handling robotics, assay quantification in 96 through 1536-well plate readers, and high throughput computing.
Aim 2 is to support clinical trials conducted at UWCCC by providing analytical chemistry expertise needed to evaluate the pharmacokinetic and pharmacodynamic properties of study drugs and to provide patient sample storage with robust and secure database documentation of all samples. DDC staff are tightly coordinated with the clinical trial enterprise at UWCCC including participation in the Cancer Therapy Discovery and Development (CTD2) group and the Disease Oriented Teams to support UWCCC members with assays for drug concentrations and biomarkers on any clinical substrate and storage of study samples from clinical trials. In the current funding period, the core provided support for 394 UWCCC studies.
Aim 3 is to train UWCCC members, their staff, and students in drug development processes and the productive application of state-of-the-art, well-maintained equipment to their specific research goals and provide 24/7 access to this drug development focused infrastructure. Impact on UWCCC: The DDC has supported the research of 128 unique UWCCC members during the current funding cycle and is well-staffed and equipped to meet the future drug development needs of UWCCC members. Continued support from the CCSG will enable highly experienced DDC staff scientists to invest time and expertise in consulting with UWCCC members on future projects and on advancing current promising molecules along the development pathway to the clinic.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA014520-46
Application #
9923033
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2020-04-01
Budget End
2021-03-31
Support Year
46
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Type
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Barault, Ludovic; Amatu, Alessio; Siravegna, Giulia et al. (2018) Discovery of methylated circulating DNA biomarkers for comprehensive non-invasive monitoring of treatment response in metastatic colorectal cancer. Gut 67:1995-2005
Long, Yin; Wei, Hao; Li, Jun et al. (2018) Effective Wound Healing Enabled by Discrete Alternative Electric Fields from Wearable Nanogenerators. ACS Nano :
Forsberg, Matthew H; Das, Amritava; Saha, Krishanu et al. (2018) The potential of CAR T therapy for relapsed or refractory pediatric and young adult B-cell ALL. Ther Clin Risk Manag 14:1573-1584
Voter, Andrew F; Killoran, Michael P; Ananiev, Gene E et al. (2018) A High-Throughput Screening Strategy to Identify Inhibitors of SSB Protein-Protein Interactions in an Academic Screening Facility. SLAS Discov 23:94-101
Thomas, Sydney P; Hoang, Trish T; Ressler, Valerie T et al. (2018) Human angiogenin is a potent cytotoxin in the absence of ribonuclease inhibitor. RNA 24:1018-1027
Johnson, Brian P; Vitek, Ross A; Geiger, Peter G et al. (2018) Vital ex vivo tissue labeling and pathology-guided micropunching to characterize cellular heterogeneity in the tissue microenvironment. Biotechniques 64:13-19
Elezaby, Mai; Li, Geng; Bhargavan-Chatfield, Mythreyi et al. (2018) ACR BI-RADS Assessment Category 4 Subdivisions in Diagnostic Mammography: Utilization and Outcomes in the National Mammography Database. Radiology 287:416-422
Tanimura, Nobuyuki; Liao, Ruiqi; Wilson, Gary M et al. (2018) GATA/Heme Multi-omics Reveals a Trace Metal-Dependent Cellular Differentiation Mechanism. Dev Cell 46:581-594.e4
Ni, Dalong; Jiang, Dawei; Ehlerding, Emily B et al. (2018) Radiolabeling Silica-Based Nanoparticles via Coordination Chemistry: Basic Principles, Strategies, and Applications. Acc Chem Res 51:778-788
Burnside, Elizabeth S; Vulkan, Daniel; Blanks, Roger G et al. (2018) Association between Screening Mammography Recall Rate and Interval Cancers in the UK Breast Cancer Service Screening Program: A Cohort Study. Radiology 288:47-54

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