The scientific goal of the Developmental Therapeutics (DT) program is to develop and evaluate novel therapeutic compounds for the treatment of cancer; this goal and DTs rapid growth was achieved in strong part to the significant expertise and expansion of the cancer center cores over the past 5 years.Through the establishment of close interactions between basic research laboratories, clinical scientists, the NCI, and the pharmaceutical industry, the most rapid development of new treatment modalities is being accomplished. Preclinical studies are conducted using novel model systems, pharmacology, and functional imaging so that the appropriate biomarkers and patient selection criteria may be incorporated into early clinical trials of targeted agents. The programmatic goals are to provide the infrastructure, including cores and clinics, to foster collaborations, in order to allow the scientific exploration of new treatment modalities. Additional recruitments are ongoing to expand the investigation of novel therapy approaches. Seminars, discussion groups, training, and courses are provided to the members. This program is organized into four major interdisciplinary research areas: Drug Discovery, Preclinical Development, Early Clinical Development, and Delivery, under the leadership of S. Gail Eckhardt, MD. Dr. Eckhardt has extensive experience in the development of novel agents and in five years has built an NCI/ U01-funded Phase I program with a national reputation. In addition, a planning grant for an AP4 (Academic Public Private Partnership) Center was awarded and the full grant will be submitted in the summer of 2005. The DT program consists of 59 (36 Full; 23 Associate) faculty members with atotal of $9.1 million in annual total costs ($3.9 million from NCI alone). The Developmental Therapeutics Program members produced a total of 456 cancer-related publications from 2000 to present. Of these, 175 (38%) are interprogrammatic and inter-/intra-programmatic publications; 117 (26%) are intra-programmatic and inter-/intraprogrammatic publications. The goals for the next five years involve substantial expansion of the faculty with recruitment into the areas of hematological malignancies and solid tumors. The preclinical imaging capabilities will be expanded to include DCE-MRI, NMR/MRS, and PET. In addition, there are plans to utilize the infrastructure and collaborations provided by the AP4 Center to build an Oncology Drug Development Center.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA046934-23
Application #
8069506
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2010-02-01
Budget End
2011-01-31
Support Year
23
Fiscal Year
2010
Total Cost
$28,496
Indirect Cost
Name
University of Colorado Denver
Department
Type
DUNS #
041096314
City
Aurora
State
CO
Country
United States
Zip Code
80045
Kim, Seongsoon; Park, Donghyeon; Choi, Yonghwa et al. (2018) A Pilot Study of Biomedical Text Comprehension using an Attention-Based Deep Neural Reader: Design and Experimental Analysis. JMIR Med Inform 6:e2
Altieri, Lisa; Miller, Kimberly A; Huh, Jimi et al. (2018) Prevalence of sun protection behaviors in Hispanic youth residing in a high ultraviolet light environment. Pediatr Dermatol 35:e52-e54
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Shearn, Colin T; Orlicky, David J; Petersen, Dennis R (2018) Dysregulation of antioxidant responses in patients diagnosed with concomitant Primary Sclerosing Cholangitis/Inflammatory Bowel Disease. Exp Mol Pathol 104:1-8
Kim, Jihye; Yoo, Minjae; Shin, Jimin et al. (2018) Systems Pharmacology-Based Approach of Connecting Disease Genes in Genome-Wide Association Studies with Traditional Chinese Medicine. Int J Genomics 2018:7697356
Coleman, Carrie B; Lang, Julie; Sweet, Lydia A et al. (2018) Epstein-Barr Virus Type 2 Infects T Cells and Induces B Cell Lymphomagenesis in Humanized Mice. J Virol 92:
Petersen, Dennis R; Orlicky, David J; Roede, James R et al. (2018) Aberrant expression of redox regulatory proteins in patients with concomitant primary Sclerosing cholangitis/inflammatory bowel disease. Exp Mol Pathol 105:32-36

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