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Ki-Ho Lee

Korea University · Medicine

About the Lab

Professor Ki-Ho Lee's research lab specializes in pharmaceutical and translational sciences, focusing on drug metabolism, toxicity mechanisms, and the development of analytical methods for veterinary drug residues. The lab investigates the molecular mechanisms underlying drug disposition and toxicity, particularly through in vitro models using human cell lines and primary tissues. Key research directions include the prediction of drug-induced liver injury via cytochrome P450-mediated bioactivation, the role of neuropeptides in neurobehavioral regulation, and the optimization of in vitro embryo production systems for agricultural and biomedical applications in pigs. The lab also emphasizes the development of rapid, reliable analytical techniques for monitoring drug residues in food and biological systems.

drug metabolismtoxicity predictionanalytical methodsveterinary drug residuesin vitro models

Research Overview

Papers
151
Total Citations
3,334
Papers (5y)
25
Primary Field
Medicine

Research Output Trend

Figures are computed from collected data and may differ slightly.

Publications per year (5y)
25total
2021
2022
2023
2024
2025
Citations per year (5y)
323total
20212022202320242025

Selected Papers

15
1
Article|122 citations·2017
An Intestine-Derived Neuropeptide Controls Avoidance Behavior in Caenorhabditis elegans
Kiho Lee, Eleftherios Mylonakis
SJR Q1Cell ReportsOA

Adjusting to a continuously changing environment is a key feature of life. For metazoans, environmental changes include alterations in the gut microbiota, which can affect both memory and behavior. The bacteriovorous nematode Caenorhabditis elegans discriminates between pathogenic and non-pathogenic food sources, avoiding the consumption of pathogens. Here, we demonstrate the role of the intestine in regulating C. elegans avoidance to Pseudomonas aeruginosa by an insulin-like neuropeptide encode

AgingBiochemistry, Genetics and Molecular Biology
2
Review|94 citations·2021
Veterinary Drug Residues in Animal-Derived Foods: Sample Preparation and Analytical Methods
Bo Wang, Kaizhou Xie, Kiho Lee
SJR Q1FoodsOA

Veterinary drugs are used to treat livestock and aquatic diseases and thus are introduced into animal-derived foods, endangering consumer health and safety. Antibiotic resistance is rapidly becoming a major worldwide problem, and there has been a steady increase in the number of pathogens that show multi-drug resistance. Illegal and excessive use of veterinary drugs in animals and aquaculture has serious adverse effects on humans and on all other environmental organisms. It is necessary to devel

PollutionEnvironmental Science
3
Article|56 citations·2009
A novel benzimidazole analogue inhibits the hypoxia-inducible factor (HIF)-1 pathway
Misun Won, Namhui Im, Soo-Hyun Park, Shanthaveerappa K. Boovanahalli, Yinglan Jin, Xuejun Jin, Kyung‐Sook Chung, Moorim Kang, Kiho Lee, Kiho Lee, Song‐Kyu Park, Hwan Mook Kim
SJR Q2Biochemical and Biophysical Research Communications
Cancer ResearchBiochemistry, Genetics and Molecular Biology
4
Article|52 citations·1999
Saturable transport of H2‐antagonists ranitidine and famotidine across Caco‐2 cell monolayers
Kiho Lee, Dhiren R. Thakker
SJR Q1Journal of Pharmaceutical Sciences

The purpose of this study was to investigate the mechanism by which the H2-antagonists ranitidine and famotidine interacted with the paracellular space during their transport across Caco-2 cell monolayers. Transport experiments with ranitidine and famotidine across Caco-2 cell monolayers were performed to determine the apical-to-basolateral flux at various concentrations. Kinetic analysis of the transport data showed that ranitidine and famotidine were transported by both saturable and nonsatura

Molecular BiologyBiochemistry, Genetics and Molecular Biology
5
Article|44 citations·2002
Secretory Transport of Ranitidine and Famotidine across Caco-2 Cell Monolayers
Kiho Lee, Chee M. Ng, Kim L. R. Brouwer, Dhiren R. Thakker
SJR Q1Journal of Pharmacology and Experimental Therapeutics
OncologyMedicine
6
Article|36 citations·2015
Prediction of Drug-Induced Liver Injury in HepG2 Cells Cultured with Human Liver Microsomes
Jong Min Choi, Soo Jin Oh, Ji-Yoon Lee, Jang Su Jeon, Chang Seon Ryu, Young‐Mi Kim, Kiho Lee, Sang Kyum Kim
SJR Q1Chemical Research in Toxicology

Drug-induced liver injury (DILI) via metabolic activation by drug-metabolizing enzymes, especially cytochrome P450 (CYP), is a major cause of drug failure and drug withdrawal. In this study, an in vitro model using HepG2 cells in combination with human liver microsomes was developed for the prediction of DILI. The cytotoxicity of cyclophosphamide, a model drug for bioactivation, was augmented in HepG2 cells cultured with microsomes in a manner dependent on exposure time, microsomal protein conce

PharmacologyPharmacology, Toxicology and Pharmaceutics
7
Article|34 citations·2009
Plasma pharmacokinetics and metabolism of the antitumour drug candidate 2′-benzoyloxycinnamaldehyde in rats
Kiho Lee, Byoung‐Mog Kwon, Kangjeon Kim, Je‐Kyung Ryu, Soo Jin Oh, Kye Sook Lee, Mu‐Gil Kwon, Song‐Kyu Park, Jong Soon Kang, Chang Woo Lee, Hwan Mook Kim
SJR Q3Xenobiotica

The pharmacokinetics and metabolism of 2'-benzoyloxycinnamaldehyde (BCA) was characterized in male Sprague-Dawley rats as part of the preclinical evaluations for developing this compound as an antitumour agent. BCA was not detected in the plasma following either intravenous or oral dose, whereas its putative metabolites 2'-hydroxycinnamaldehyde (HCA) and o-coumaric acid were present at considerable levels. In separate pharmacokinetics studies, HCA exhibited a high systemic clearance and a large

PharmacologyPharmacology, Toxicology and Pharmaceutics
8
Article|29 citations·2022
Production of Pigs From Porcine Embryos Generated in vitro
Paula R. Chen, Kyungjun Uh, Bethany K. Redel, Emily D. Reese, Randall S. Prather, Kiho Lee
SJR Q1Frontiers in Animal ScienceOA

Generating porcine embryos in vitro is a critical process for creating genetically modified pigs as agricultural and biomedical models; however, these embryo technologies have been scarcely applied by the swine industry. Currently, the primary issue with in vitro -produced porcine embryos is low pregnancy rate after transfer and small litter size, which may be exasperated by micromanipulation procedures. Thus, in this review, we discuss improvements that have been made to the in vitro porcine em

GeneticsBiochemistry, Genetics and Molecular Biology
9
Article|16 citations·2020
Short term relief of multisite chronicpain with Bowen Therapy: A double-blind, randomized controlled trial
Kiho Lee, Gwyn N. Lewis
SJR Q1Journal of Bodywork and Movement Therapies
PharmacologyMedicine
10
Article|16 citations·2021
Synthesis and Biochemical Evaluation of Baicalein Prodrugs
Sang‐Hyun Son, Jinhong Kang, Myunghwan Ahn, So‐Yeon Nam, Yong Woo Jung, Ki Yong Lee, Ki Yong Lee, Young Ho Jeon, Youngjoo Byun, Kiho Lee, Kiho Lee
SJR Q1PharmaceuticsOA

Baicalein (5,6,7-trihydroxy-2-phenyl-4H-1-benzopyran-4-one), a flavonoid analog from Scutellaria baicalensis, possesses several pharmacological activities including antioxidant, antiproliferative, and anti-inflammatory activities. We previously reported that baicalein inhibits the thymic stromal lymphopoietin (TSLP)/TSLP receptor (TSLPR) signaling pathways and can be used as an active ingredient in the treatment of asthma and atopic dermatitis. However, baicalein is rapidly metabolized to baical

PharmacologyMedicine
11
Article|16 citations·2013
Pharmacokinetics and Metabolism of 4‐O‐Methylhonokiol in Rats
Hyung Eun Yu, Soo Jin Oh, Je Kyung Ryu, Jong Soon Kang, Jin Tae Hong, Jae‐Kyung Jung, Sang‐Bae Han, Seung‐Yong Seo, Young Heui Kim, Song‐Kyu Park, Hwan Mook Kim, Kiho Lee
SJR Q1Phytotherapy Research

The purpose of this study was to characterize the pharmacokinetics and metabolism of 4-O-methylhonokiol in rats. The absorption and disposition of 4-O-methylhonokiol were investigated in male Sprague-Dawley rats following a single intravenous (2 mg/kg) or oral (10 mg/kg) dose. Its metabolism was studied in vitro using rat liver microsomes and cytosol. 4-O-Methylhonokiol exhibited a high systemic plasma clearance and a large volume of distribution. The oral dose gave a peak plasma concentration o

RehabilitationMedicine
12
Article|13 citations·2021
Identification of Erythromycin and Clarithromycin Metabolites Formed in Chicken Liver Microsomes Using Liquid Chromatography–High-Resolution Mass Spectrometry
Bo Wang, So‐Yeon Nam, Eunyeong Kim, Hayoung Jeon, Kiho Lee, Kaizhou Xie
SJR Q1FoodsOA

Nontargeted analysis can be used for the rapid screening and confirmatory analysis of veterinary drugs and their metabolites, which are important for the comprehensive safety evaluation of animal-derived foods. Here, a novel nontargeted screening approach based on liquid chromatography coupled with electrospray ionization-high-resolution mass spectrometry (LC/ESI-HR-MS) was developed to determine erythromycin, clarithromycin, and their metabolites in chicken liver microsomes. Erythromycin and cl

PharmacologyMedicine
13
Article|12 citations·2017
Synthesis, biological evaluation, and metabolic stability of chlorogenic acid derivatives possessing thiazole as potent inhibitors of α-MSH-stimulated melanogenesis
Hyeju Jo, Yuanyuan Zhou, Mayavan Viji, Min-Ho Choi, Jae Young Lim, Jaeuk Sim, Jeongtae Rhee, Young Soo Kim, Seung‐Yong Seo, Wun‐Jae Kim, Jin Tae Hong, Heesoon Lee
SJR Q2Bioorganic & Medicinal Chemistry Letters
Cell BiologyBiochemistry, Genetics and Molecular Biology
14
Article|11 citations·2018
Iodine‐Promoted One‐pot Synthesis of Highly Substituted 4‐Aminopyrroles and Bis‐4‐aminopyrrole from Aryl Methyl Ketones, Arylamines, and Enamines
Hitesh B. Jalani, Jyotirling R. Mali, Hyejun Park, Jae Kyun Lee, Kiho Lee, Kiho Lee, Kyeong Lee, Kyeong Lee, Yongseok Choi
SJR Q1Advanced Synthesis & Catalysis

Abstract An iodine‐promoted one‐pot synthesis of functionally diverse and highly substituted 4‐aminopyrroles directly from aryl methyl ketones, arylamines, and enamines was developed. The reaction involves in‐situ oxidation of aryl methyl ketone to glyoxal, subsequent imine formation by aniline, followed by nucleophilic addition of enamine, and cyclization to afford highly substituted 4‐aminopyrroles. This reaction involved the formation of two C−N bonds and one C−C bond by a formal [1+1+3] annu

Organic ChemistryChemistry
15
Article|10 citations·2018
Transition-metal-free, atom-economical cascade synthesis of novel 2-sulfonated-benzo[f][1,7]naphthyridines and their cytotoxic activities
Sateesh Kumar Arepalli, Yunseon Choi, Kiho Lee, Jong Soon Kang, Jae‐Kyung Jung, Heesoon Lee
SJR Q3Tetrahedron
Organic ChemistryChemistry

Research Areas

PharmacologyCancer ResearchMolecular BiologyOrganic ChemistryImmunologyRehabilitation

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