Young Ju Kwon
Korea University · Medicine
About the Lab
Professor Young Ju Kwon's research lab focuses on translational biomedical research with a strong emphasis on cancer biology, fibrosis, and protein-based therapeutics. The lab investigates molecular mechanisms underlying aggressive cancers such as triple-negative breast cancer and epithelial ovarian cancer, particularly under hypoxic conditions, and explores novel therapeutic targets like transcription factors (e.g., ELF3) and signaling pathways. It also develops innovative nanotherapeutic strategies, including hyaluronic acid-bilirubin nanoparticles for targeting activated hepatic stellate cells in liver fibrosis, and investigates protein stability and modification in therapeutic albumin formulations. The lab integrates molecular biology, chemical design, and nanomedicine to address unmet clinical needs in oncology and fibrotic diseases.
Research Overview
Research Output Trend
Figures are computed from collected data and may differ slightly.
Selected Papers
15Breast cancer accounts for 25% of all types of cancer in women, and triple negative breast cancer (TNBC) comprises around 15~20% of breast cancers. Conventional chemotherapy and radiation are the primary systemic therapeutic strategies; no other FDA-approved targeted therapies are yet available as for TNBC. TNBC is generally characterized by a poor prognosis and high rates of proliferation and metastases. Due to these aggressive features and lack of targeted therapies, numerous attempts have bee
A series of novel terpyridine-skeleton molecules containing conformational rigidity, 14 containing benzo[4,5]furo[3,2-b]pyridine core and 15 comprising chromeno[4,3-b]pyridine core, were synthesized, and their biological activities were evaluated. 3-(4-Phenylbenzo[4,5]furo[3,2-b]pyridin-2-yl)phenol (8) was determined to be a nonintercalative topo I and II dual catalytic inhibitor and 3-(4-phenylchromeno[4,3-b]pyridine-2-yl)phenol (22) was determined to be a nonintercalative topo IIα specific cat
Liver fibrosis is a life-threatening and irreversible disease. The fibrosis process is largely driven by hepatic stellate cells (HSCs), which undergo transdifferentiation from an inactivated state to an activated one during persistent liver damage. This activated state is responsible for collagen deposition in liver tissue and is accompanied by increased CD44 expression on the surfaces of HSCs and amplified intracellular oxidative stress, which contributes to the fibrosis process. To address thi
Regulation of gene expression by transcription factors touches many aspects of eukaryotic biology, and its systematic, external control by organic molecules represents a challenge in chemistry. Here we report the design of a completely organic, nonpeptidic compound that mimics a transcription factor. The design takes advantage of the specific DNA-binding affinity of a hairpin polyamide molecule and the ability of wrenchnolol to bind to the Sur-2 subunit of human mediator complex. The hybrid comp
This study based on the person-environment fit theory, giving a definition of job stress. Job stress is defined as unfit between person and environment and type of unfit is classified need-supplies unfit and abilities-demand unfit. Using this concept as a basis, it is analysed that social support type moderates teachers' burnout according to job stressors. The results indicate that social supports have a buffering effects or reverse buffering effect according to interaction of job stressors and
Research Areas
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