Current preclinical high-throughput drug screening methods are time-consuming and expensive. Moreover, most of the candidates generated during screenings turn out to be invalid after further testing in animal models. To overcome these limitations, efforts are now being made to develop noninvasive, highly sensitive and cost-effective imaging tools for monitoring and early detection of drug efficacy in single cells and in vivo. Activatable imaging probes are designed to amplify or boost fluorescence signals in response to recognition of specific biomolecular interactions. We developed various protease-activatable systems for imaging and diagnostic applications by using advanced nanobioconjugation chemistry with fluorophores, peptides, polymers and metals. In this proposal, we plan to expand those research findings to a novel preclinical drug screening system for the rapid characterization of apoptosis-related drug candidates. Because the most effective anticancer therapeutics mediate apoptosis cascades, real time screening methods to detect the progression of apoptosis at the molecular level in single cells in vitro and in vivo would significantly improve the understanding of intracellular apoptotic signal mechanisms and could assist the clinical monitoring and screening of apoptosis-related drug efficacy. We will develop advanced screening technologies that can be applied in cell-based high-throughput and in vivo drug screening for next generation drugs targeting apoptosis. Different types of activatable imaging systems that target crucial apoptosis mediators, caspases, will be developed and optimized for in vitro and in vivo applications. By targeting a crucial apoptosis mediator, the early stage of apoptosis can be readily monitored, imaged and analyzed in a rapid and efficient fashion. Selected screening systems will be validated in various experimental models of tumor apoptosis. Standard in vitro and in vivo drug screening methods will be drafted. Overall, this system is expected to significantly reduce time and costs associated with drug screening tests in animals.
Our aim i s to develop fully translatable preclinical screening systems for drug discovery targeting apoptosis. Success of the proof-of-concept illustrated in this initiative will allow for widespread preclinical and clinical applications.
In this proposal, advanced preclinical high-throughput screening systems will be developed for next generation drugs targeting apoptosis. Overall, this system is expected to significantly reduce time and costs associated with drug screening at preclinical stages and will also promote the understanding of complicated apoptotic processes in pathologies.
|Oh, Yumin; Park, Ogyi; Swierczewska, Magdalena et al. (2016) Systemic PEGylated TRAIL treatment ameliorates liver cirrhosis in rats by eliminating activated hepatic stellate cells. Hepatology 64:209-23|
|Swierczewska, M; Han, H S; Kim, K et al. (2016) Polysaccharide-based nanoparticles for theranostic nanomedicine. Adv Drug Deliv Rev 99:70-84|
|Swierczewska, Magdalena; Lee, Kang Choon; Lee, Seulki (2015) What is the future of PEGylated therapies? Expert Opin Emerg Drugs 20:531-6|
|Oh, Yumin; Swierczewska, Magdalena; Kim, Tae Hyung et al. (2015) Delivery of tumor-homing TRAIL sensitizer with long-acting TRAIL as a therapy for TRAIL-resistant tumors. J Control Release 220:671-81|
|Kim, Tae Hyung; Swierczewska, Magdalena; Oh, Yumin et al. (2013) Mix to validate: a facile, reversible PEGylation for fast screening of potential therapeutic proteins in vivo. Angew Chem Int Ed Engl 52:6880-4|
|Kim, Tae Hyung; Lee, Seulki; Chen, Xiaoyuan (2013) Nanotheranostics for personalized medicine. Expert Rev Mol Diagn 13:257-69|