The Cancer Therapeutics Program (CTP) is organized around three Research Themes: 1) Target Identification and Drug Discovery; 2) Drug Development; and 3) Clinical Investigations and Translational Studies. In Theme 1, biomarker and drug leads are discovered by multi-disciplinary teams and subsequently prioritized for further development by Program Leaders. Since many tools used for the development of cancer therapeutics can also be applied for tumor marker, Theme 1 encompasses projects that focus on the following technologies: ?Omics, [genomics, proteomics, metabolomics, and glycomics], combinatorial chemistry, medicinal chemistry, organic synthesis, carbohydrate chemistry and biosynthesis, computational and structural biology [including cryto-TEM, AFM and X-ray crystallography], high-throughput screening, nanotechnology, cancer stem cells, immunotherapy, and microRNA targeting. Theme 2 specifically focuses on preclinical anti- cancer drug development projects, including efforts to understand drug-target interactions, compensatory feedback effects and resistance mechanisms in order to form the basis and rationale for early phase clinical trial investigations. Theme 2 also encompasses the development of robust laboratory resources essential for preclinical drug modeling (e.g., patient derived xenograft [PDX] models and pharmacokinetics). Theme 3 focuses on the direct translation of preclinical models to human applications in the context of clinical trial design and conduct. In addition, Theme 3 also includes biospecimen collection and subsequent bedside-to- bench translational studies of these specimens in order to further evaluate pharmacodynamic effects and resistance mechanisms. The mission of the CTP is realized by the following Specific Aims: 1) Enhance and facilitate intra- programmatic and inter-programmatic interaction and collaboration between basic scientists and clinical investigators in cancer therapeutics; 2) Promote the discovery, development, and application of novel therapeutic approaches; and, 3) Develop translational and laboratory-based clinical investigations of new therapeutic agents and new therapeutic approaches. PROGRAM ASPECTS Co-leaders: Kit S. Lam, MD, PhD; Primo N. Lara, Jr. MD Members: 55 Total Grant Funding (ADC): $8.7 million Total Peer-Reviewed Funding (ADC): $5.2 million Total NCI funding (ADC): $2.2 million Total No. Publications: 824 Inter-programmatic publications: 265 (32.2%) Intra-programmatic publications: 271 (32.9%) Multi-institutional publications: 384 (46.6%) The CTP has 55 members from 14 diverse academic units of UC Davis including Biochemistry and Molecular Medicine, Chemistry, Entomology and Nematology, Biomedical Engineering, Dermatology, Internal Medicine, Molecular and Cellular Biology, Neurology, Obstetrics and Gynecology, Pediatrics, Pharmacology, Radiation Oncology, and Surgery, and 6 different schools highlighting the multidisciplinary focus of the program. The total peer-reviewed, cancer-related funding (annual direct cost) has slightly declined to $5.2 million ($2.2 million NCI) from $8.8 million at the last competitive renewal ($3.8 million NCI) due to sequestration and the transition of Urothelial Cancer-related funding from this program to the new Prostate Urothelial Cancer Program (Program 5). Despite the decrease in funding, our funded projects have increased with 55 peer-review funded projects (27 NCI-funded) compared to 52 peer-review funded projects (25 NCI-funded) at the last competitive renewal.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA093373-15
Application #
9327889
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2017-07-01
Budget End
2018-06-30
Support Year
15
Fiscal Year
2017
Total Cost
Indirect Cost
Name
University of California Davis
Department
Type
DUNS #
047120084
City
Davis
State
CA
Country
United States
Zip Code
95618
Shih, Tsung-Chieh; Liu, Ruiwu; Wu, Chun-Te et al. (2018) Targeting Galectin-1 Impairs Castration-Resistant Prostate Cancer Progression and Invasion. Clin Cancer Res 24:4319-4331
Weiss, Robert H (2018) Metabolomics and Metabolic Reprogramming in Kidney Cancer. Semin Nephrol 38:175-182
Hegde, John V; Shaverdian, Narek; Daly, Megan E et al. (2018) Patient-reported quality-of-life outcomes after de-escalated chemoradiation for human papillomavirus-positive oropharyngeal carcinoma: Findings from a phase 2 trial. Cancer 124:521-529
Arun, Adith S; Tepper, Clifford G; Lam, Kit S (2018) Identification of integrin drug targets for 17 solid tumor types. Oncotarget 9:30146-30162
Tepper, Clifford G; Dang, Julie H T; Stewart, Susan L et al. (2018) High frequency of the PNPLA3 rs738409 [G] single-nucleotide polymorphism in Hmong individuals as a potential basis for a predisposition to chronic liver disease. Cancer 124 Suppl 7:1583-1589
Jerant, Anthony; Fenton, Joshua J; Kravitz, Richard L et al. (2018) Association of Clinician Denial of Patient Requests With Patient Satisfaction. JAMA Intern Med 178:85-91
Kirschbaum, Mark H; Frankel, Paul; Synold, Timothy W et al. (2018) A phase II study of vascular endothelial growth factor trap (Aflibercept, NSC 724770) in patients with myelodysplastic syndrome: a California Cancer Consortium Study. Br J Haematol 180:445-448
Besprozvannaya, Marina; Dickson, Eamonn; Li, Hao et al. (2018) GRAM domain proteins specialize functionally distinct ER-PM contact sites in human cells. Elife 7:
Turner, David C; Kondic, Anna G; Anderson, Keaven M et al. (2018) Pembrolizumab Exposure-Response Assessments Challenged by Association of Cancer Cachexia and Catabolic Clearance. Clin Cancer Res 24:5841-5849
Matsumoto, Collin; Jiang, Yan; Emathinger, Jacqueline et al. (2018) Short Telomeres Induce p53 and Autophagy and Modulate Age-Associated Changes in Cardiac Progenitor Cell Fate. Stem Cells 36:868-880

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