Lead Development and Optimization Shared Resource The Lead Development and Optimization (LDO) shared resource is a mission critical element of KUCC that allows us to redefine translational research in an academic cancer center. It is a key component of the Cancer Center's strategy to optimize the rapid movement of basic research findings into new therapeutic advances either through traditional lead compound development and optimization, or drug repurposing strategies. The LDO fosters translational research by: 1) providing support to researchers and clinicians engaged in the discovery and development of novel therapeutics for treatment and prevention of cancer, 2) providing drug discovery, delivery and development expertise to KUCC translational research projects, and 3) supporting key collaborations with industry, academic, government and disease philanthropy organizations with whom we have established collaborations in support of the goals and themes of our scientific research programs. The LDO, directed by Michael J. Baltezor, PhD, is a multi-component shared resource that provides unique expertise and capabilities in drug discovery, delivery, and development that is rarely available in an academic setting. Through a combination of highly trained, industry-experienced scientists and state-of the- art equipment the LDO is capable of supporting the development of novel cancer therapeutics in the following preclinical spaces: 1) Drug Discovery High Throughput Screening (HTS) - research and development focused on target selection and validation for high throughput method development and compound probe screening; 2) Drug Delivery Biotechnology Innovation and Optimization Facility (BIOF) - research and development focused on conventional and novel drug delivery and animal pharmacokinetic support; 3) Preclinical Proof of Concept (PPOC) - in vitro lead optimization and development of new and improved animal models for cancer to test lead molecules with capabilities to perform whole animal imaging in rodents. The LDO provided support for 51 research projects in 2010, 32 (62%) were led by KUCC members. During the past three years the LDO was instrumental in helping advance five drug therapies by KUCC investigators into Phase I clinical trials and to do so in a cost effective and efficient manner. Overall, Cancer Center members with peer-reviewed research funding used approximately 75% of the LDO's capacity.
The services provided by the LDO shared resource are available to researchers to facilitate the advancement of investigative drugs through the early stages of drug development. The skills necessary to conduct high throughput screening, drug delivery and preclinical proof of concept studies are not always easily available or affordable for academic investigators. The LDOSR addresses this need and allows investigators to concentrate on moving their research forward.
| Gonzalez-Mercado, Velda J; Fridley, Brooke L; Saligan, Leorey N (2018) Sestrin family of genes and their role in cancer-related fatigue. Support Care Cancer 26:2071-2074 |
| Rebbeck, Timothy R (see original citation for additional authors) (2018) Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations. Hum Mutat 39:593-620 |
| Roy, Anuradha (2018) Early Probe and Drug Discovery in Academia: A Minireview. High Throughput 7: |
| Lea, Wendy A; Parnell, Stephen C; Wallace, Darren P et al. (2018) Human-Specific Abnormal Alternative Splicing of Wild-Type PKD1 Induces Premature Termination of Polycystin-1. J Am Soc Nephrol 29:2482-2492 |
| Hirst, Jeff; Pathak, Harsh B; Hyter, Stephen et al. (2018) Licofelone Enhances the Efficacy of Paclitaxel in Ovarian Cancer by Reversing Drug Resistance and Tumor Stem-like Properties. Cancer Res 78:4370-4385 |
| Trinca, Gloria M; Goodman, Merit L; Papachristou, Evangelia K et al. (2018) O-GlcNAc-Dependent Regulation of Progesterone Receptor Function in Breast Cancer. Horm Cancer 9:12-21 |
| Subramaniam, Dharmalingam; Kaushik, Gaurav; Dandawate, Prasad et al. (2018) Targeting Cancer Stem Cells for Chemoprevention of Pancreatic Cancer. Curr Med Chem 25:2585-2594 |
| Beadnell, Thomas C; Scheid, Adam D; Vivian, Carolyn J et al. (2018) Roles of the mitochondrial genetics in cancer metastasis: not to be ignored any longer. Cancer Metastasis Rev : |
| Li, Linda Xiaoyan; Zhou, Julie Xia; Calvet, James P et al. (2018) Lysine methyltransferase SMYD2 promotes triple negative breast cancer progression. Cell Death Dis 9:326 |
| Peng, Weidan; Furuuchi, Narumi; Aslanukova, Ludmila et al. (2018) Elevated HuR in Pancreas Promotes a Pancreatitis-Like Inflammatory Microenvironment That Facilitates Tumor Development. Mol Cell Biol 38: |
Showing the most recent 10 out of 177 publications
