Joo-Hee Lee
Hanyang University · Medicine
About the Lab
Professor Joo-Hee Lee's research lab focuses on the molecular mechanisms underlying cellular aging, inflammation, and cancer therapy resistance, with a particular emphasis on epigenetic regulation and inflammatory signaling pathways. The lab investigates how senescence and chronic inflammation—particularly 'inflammaging'—contribute to skin aging and fibrotic scarring, while also exploring therapeutic strategies targeting key molecules such as thymidylate synthase, HMGB-1, and HDAC10. A central theme is the development of novel interventions using epigenetic modulators (e.g., HDAC inhibitors) and bioactive molecules (e.g., PDRN, hyaluronic acid) to treat age-related and inflammatory diseases.
Research Overview
Research Output Trend
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Selected Papers
15Cellular senescence and aging result in a reduced ability to manage persistent types of inflammation. Thus, the chronic low-level inflammation associated with aging phenotype is called "inflammaging". Inflammaging is not only related with age-associated chronic systemic diseases such as cardiovascular disease and diabetes, but also skin aging. As the largest organ of the body, skin is continuously exposed to external stressors such as UV radiation, air particulate matter, and human microbiome. I
Thymidylate synthase (TS) overexpression is a key determinant of 5-fluorouracil (5-FU) resistance in human cancer cells. TS is also acutely up-regulated with 5-FU treatment, and, thus, novel strategies targeting TS down-regulation seem to be promising in terms of modulating 5-FU resistance. Here, we report that histone deacetylase inhibitors can reverse 5-FU resistance by down-regulating TS. By using cDNA microarrays and validation experiments, we found that trichostatin A reduced the expression
This research showed that new teaching and learning methods designed to improve critical thinking were generally effective at enhancing critical thinking dispositions.
High-mobility group box protein-1 (HMGB-1) plays a central role in the inflammatory network, and uncontrolled chronic inflammation can lead to excessive scarring. The aim of this study was to evaluate the anti-inflammatory effects of polydeoxyribonucleotide (PDRN) on scar formation. Sprague-Dawley rats (n = 30) underwent dorsal excision of the skin, followed by skin repair. PDRN (8 mg/kg) was administered via intraperitoneal injection for three (PDRN-3 group, n = 8) or seven (PDRN-7 group, n = 8
BACKGROUND: Hyaluronic acid (HA) is a primary component of the extracellular matrix, and the efficacy of HA on oral ulcers is rarely reported. OBJECTIVE: To observe the efficacy and safety of the topical application of 0.2% HA gel on recurrent oral ulcers and to compare its effects in patients with recurrent aphthous ulcers (RAU) and the oral ulcers of Behçet's disease (BD). MATERIALS AND METHODS: Thirty-three outpatients with recurrent oral ulcers were included in the study (17 patients: BD, 16
Histone deacetylase (HDAC)10, a novel class IIb histone deacetylase, is the most similar to HDAC6, since both contain a unique second catalytic domain. Unlike HDAC6, which is located in the cytoplasm, HDAC10 resides in both the nucleus and cytoplasm. The transcriptional targets of HDAC10 that are associated with HDAC10 gene regulation have not been identified. In the present study, we found that knockdown of HDAC10 significantly increased the mRNA expression levels of thioredoxin-interacting pro
Drug-induced haploinsufficiency (DIH) in yeast has been considered a valuable tool for drug target identification. A plant metabolite, plumbagin, has potent anticancer activity via reactive oxygen species (ROS) generation. However, the detailed molecular targets of plumbagin for ROS generation are not understood. Here, using DIH and heterozygous deletion mutants of the fission yeast Schizosaccharomyces pombe, we identified 1, 4-phopshatidylinositol 5-kinase (PI5K) its3 as a new molecular target
// Ju-Hee Lee 1,2 , Ji-Hong Moon 1,2 , Sung-Wook Kim 1,2 , Jae-Kyo Jeong 1,2 , Uddin MD. Nazim 1,2 , You-Jin Lee 1,2 , Jae-Won Seol 1 and Sang-Youel Park 1,2 1 Biosafety Research Institute, College of Veterinary Medicine, Chonbuk National University, Jeonju, Jeonbuk, South Korea 2 Department of Bioactive Material Sciences and Research Center of Bioactive Materials, Chonbuk National University, Jeonju, Jeonbuk, South Korea Correspondence to: Jae-Won Seol, email: // Sang-Youel Park, email: // Keyw
BACKGROUND AND OBJECTIVE: Acne scarring is a common complication of acne but no effective single treatment modality has been developed. To compare the efficacy of 1,550 nm Er:Glass fractional laser and chemical reconstruction of skin scar (CROSS) method in the treatment of acne scars. STUDY DESIGN/MATERIALS AND METHODS: A split-face trial was conducted in 20 patients (10 rolling, 10 icepick types) with acne scars. One side was treated with the 1,550 nm Er:Glass fractional laser three times with
Research Areas
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