The Sidney Kimmel Comprehensive Cancer Center (SKCCC) Analytical Pharmacology Core (APC) has offered state-of-the-art and cost-effective analytical chemistry and clinical pharmacology services to members continuously since its inception in 1985. The APC provides instrumentation and facilities in a 1,200 ft2 laboratory on the first floor of the SKCCC Bunting-Blaustein Cancer Research Building (CRBI).
The specific aims of this Core are to: 1) provide expertise in clinical trial and preclinical study design, with a focus on critical pharmacological endpoints; 2) provide state-of-the-art, Good Laboratory Practice (GLP)-quality, cost- effective services to quantitate anticancer drugs and metabolites in biological fluids; and 3) provide pharmacokinetic/ pharmacodynamic data analysis and interpretation, with the long-term vision of providing decision tools for drug development in both the preclinical and clinical settings. The APC houses four ultra- performance liquid chromatography/high-performance liquid chromatography (UPLC/HPLC) instruments with a UV/fluorescence (1), triple-stage quadruple mass spectrometer (3) and a QTrap system with ion trap capabilities (1) for more intricate drug metabolism studies. The APC analyzes over 3,200 samples/year, develops 15 new methods per year and serves over 45 faculty members across all of the CCSG Programs, with the majority of the users having peer-reviewed funding. During the last five years, the APC has become a critical component across the translational spectrum, providing services in analytical method development (four manuscripts), drug discovery (seven manuscripts), preclinical studies (26 manuscripts) and clinical trials (31 manuscripts). The APC has participated in the submission of 42 cancer-focused grants over five years, played a major role in the successful applications for the Johns Hopkins Early Therapeutics Clinical Trials Network (UM1) and AIDS Malignancy Consortium (UM1), and served as a second laboratory for the Adult Brain Tumor Consortium (UM1). The requested CCSG funding will support personnel who provide consultative services related to assay development, protocol design and data interpretation, and ensure that instrumentation is suitably maintained and utilized efficiently. SKCCC Managed Core Reporting Period: Jan. 1, 2015, to Dec. 31, 2015

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA006973-55
Application #
9519878
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2018-05-01
Budget End
2019-04-30
Support Year
55
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Type
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21205
Antonarakis, Emmanuel S; Lu, Changxue; Luber, Brandon et al. (2018) Germline DNA-repair Gene Mutations and Outcomes in Men with Metastatic Castration-resistant Prostate Cancer Receiving First-line Abiraterone and Enzalutamide. Eur Urol 74:218-225
Zarif, Jelani C; Antonarakis, Emmanuel S (2018) Targeting ELK1: a wELKome addition to the prostate cancer armamentarium. AME Med J 3:
Martino, Thiago; Kudrolli, Tarana A; Kumar, Binod et al. (2018) The orally active pterocarpanquinone LQB-118 exhibits cytotoxicity in prostate cancer cell and tumor models through cellular redox stress. Prostate 78:140-151
Isaacsson Velho, Pedro; Antonarakis, Emmanuel S (2018) PD-1/PD-L1 pathway inhibitors in advanced prostate cancer. Expert Rev Clin Pharmacol 11:475-486
Schoch, Laura K; Cooke, Kenneth R; Wagner-Johnston, Nina D et al. (2018) Immune checkpoint inhibitors as a bridge to allogeneic transplantation with posttransplant cyclophosphamide. Blood Adv 2:2226-2229
Cuviello, Andrea; Goyal, Anshit; Zick, Aviad et al. (2018) Sporadic Malignant Glomus Tumor of the Brachial Plexus With Response to Targeted Therapy Directed Against Oncogenic BRAF. JCO Precis Oncol 2018:
Giraldo, Nicolas A; Nguyen, Peter; Engle, Elizabeth L et al. (2018) Multidimensional, quantitative assessment of PD-1/PD-L1 expression in patients with Merkel cell carcinoma and association with response to pembrolizumab. J Immunother Cancer 6:99
Barberi, Theresa; Martin, Allison; Suresh, Rahul et al. (2018) Absence of host NF-?B p50 induces murine glioblastoma tumor regression, increases survival, and decreases T-cell induction of tumor-associated macrophage M2 polarization. Cancer Immunol Immunother 67:1491-1503
Taube, Janis M; Galon, Jérôme; Sholl, Lynette M et al. (2018) Implications of the tumor immune microenvironment for staging and therapeutics. Mod Pathol 31:214-234
Krueger, Timothy E G; Thorek, Daniel L J; Denmeade, Samuel R et al. (2018) Concise Review: Mesenchymal Stem Cell-Based Drug Delivery: The Good, the Bad, the Ugly, and the Promise. Stem Cells Transl Med 7:651-663

Showing the most recent 10 out of 2393 publications