CORE-012: PHARMACOANALYTICAL SHARED RESOURCE (PhASR) PROJECT SUMMARY / ABSTRACT The Ohio State University Comprehensive Cancer Center (OSUCCC) Pharmacoanalytical Shared Resource (PhASR) provides critical support to OSUCCC's robust drug development efforts, highlighted by a robust clinical trials program that has increased therapeutic accruals by 51% during the prior grant period and notable because the OSUCCC is one of only five institutions with both an NCI clinical trials UM1 Phase I grant and N01 Phase II contract. PhASR's Specific Aims are: 1) development and validation of new assays to quantify drugs and metabolites in biological specimens; 2) quantify drug and metabolite levels in biological matrices, and conduct pharmacokinetic (PK) and pharmacodynamic (PD) studies for incorporation into pre-clinical and clinical decision-making; and, 3) provide expertise in PK/PD study design and data interpretation to support submission of clinical protocols, grants, and publications. PhASR is directed by Dr. Mitchell Phelps (LR) and the Senior Faculty Advisor is Dr. Michael Grever (LR). Located within the Biomedical Research Tower, PhASR is accessible to most OSUCCC cancer researchers, and is directly across from the new James Cancer Hospital. Outstanding institutional support is provided by the OSUCCC, College of Pharmacy, and Center for Clinical and Translational Science. Major equipment in PhASR includes 5 LC-MS systems ideally suited for drug quantification and metabolite identification, namely a quadrupole-time-of-flight, an ion trap, and three triple-quadrupole mass spectrometers, supported by ultra-high pressure liquid chromatography systems and automated sample processing for high throughput analysis. The Dionex RSLCnano/TSQ Quantiva mass spectrometer is the most advanced on the market. During the prior grant period, PhASR provided services to 50 OSUCCC members, representing all 5 programs, and developed more than 120 assays. It has provided 14,416 hours of services as well as assays for 2024 samples during the prior grant period. PhASR has contributed to over 79 publications (7 with an impact factor >10), contributed data for 41 grant applications and has supported 53 clinical trials. In the future, the PhASR will enhance its support for the OSUCCC Drug Development Institute (DDI), and increase both its pharmacodynamic and modeling services, and recruit additional faculty in pharmaceutics. The annual budget is $744,732, yet the CCSG request is $77,729. The PhASR leverages extensive institutional support and seeks only 10.4% support from CCSG funds. The Pharmacoanalytical Shared Resource is part of the Analytics Grouping.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA016058-43
Application #
9632726
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2018-12-01
Budget End
2019-11-30
Support Year
43
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Ohio State University
Department
Type
DUNS #
832127323
City
Columbus
State
OH
Country
United States
Zip Code
43210
Norquist, Barbara M; Brady, Mark F; Harrell, Maria I et al. (2018) Mutations in Homologous Recombination Genes and Outcomes in Ovarian Carcinoma Patients in GOG 218: An NRG Oncology/Gynecologic Oncology Group Study. Clin Cancer Res 24:777-783
Zhang, Bin; Nguyen, Le Xuan Truong; Li, Ling et al. (2018) Bone marrow niche trafficking of miR-126 controls the self-renewal of leukemia stem cells in chronic myelogenous leukemia. Nat Med 24:450-462
Tasselli, Giorgia; Filippucci, Sara; Borsella, Elisabetta et al. (2018) Yeast lipids from cardoon stalks, stranded driftwood and olive tree pruning residues as possible extra sources of oils for producing biofuels and biochemicals. Biotechnol Biofuels 11:147
Moliva, J I; Hossfeld, A P; Canan, C H et al. (2018) Exposure to human alveolar lining fluid enhances Mycobacterium bovis BCG vaccine efficacy against Mycobacterium tuberculosis infection in a CD8+ T-cell-dependent manner. Mucosal Immunol 11:968-978
Suarez-Kelly, Lorena P; Akagi, Keiko; Reeser, Julie W et al. (2018) Metaplastic breast cancer in a patient with neurofibromatosis type 1 and somatic loss of heterozygosity. Cold Spring Harb Mol Case Stud 4:
Malpeli, Giorgio; Barbi, Stefano; Greco, Corinna et al. (2018) MicroRNA signatures and Foxp3+ cell count correlate with relapse occurrence in follicular lymphoma. Oncotarget 9:19961-19979
Talbert, Erin E; Lewis, Heather L; Farren, Matthew R et al. (2018) Circulating monocyte chemoattractant protein-1 (MCP-1) is associated with cachexia in treatment-naïve pancreatic cancer patients. J Cachexia Sarcopenia Muscle 9:358-368
Wang, Jin-Ting; Xie, Wen-Quan; Liu, Fa-Quan et al. (2018) NADH protect against radiation enteritis by enhancing autophagy and inhibiting inflammation through PI3K/AKT pathway. Am J Transl Res 10:1713-1721
Karpurapu, Manjula; Lee, Yong Gyu; Qian, Ziqing et al. (2018) Inhibition of nuclear factor of activated T cells (NFAT) c3 activation attenuates acute lung injury and pulmonary edema in murine models of sepsis. Oncotarget 9:10606-10620
Behnfeldt, Julia Harris; Acharya, Samir; Tangeman, Larissa et al. (2018) A tri-serine cluster within the topoisomerase II?-interaction domain of the BLM helicase is required for regulating chromosome breakage in human cells. Hum Mol Genet 27:1241-1251

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