Skip to main content

Misu Dong

Ewha Womans University · Medicine

About the Lab

Professor Misu Dong's research lab specializes in pharmacogenomics, drug metabolism, and toxicology, with a focus on understanding the genetic and enzymatic factors influencing drug response and toxicity. The lab investigates cytochrome P450 and flavin-containing monooxygenase (FMO) enzyme activities, particularly in relation to drug metabolism and individual variability in drug response. Key research directions include the development of non-invasive phenotyping methods for drug-metabolizing enzymes, the role of genetic polymorphisms (e.g., CYP2C19, MDR1) in drug efficacy and safety, and the mechanisms of endocrine disruption by environmental chemicals. The lab also explores innovative in vitro models to replace traditional metabolic activation systems in genotoxicity testing.

pharmacogenomicsdrug metabolismcytochrome P450FMO phenotypingtoxicology

Research Overview

Papers
54
Total Citations
1,132
Papers (5y)
9
Primary Field
Medicine

Research Output Trend

Figures are computed from collected data and may differ slightly.

Publications per year (5y)
9total
2015
2016
2017
2021
2024
Citations per year (5y)
134total
20152016201720212024

Selected Papers

15
1
Article|124 citations·1997
Reconstitution of Recombinant Cytochrome P450 2C10(2C9) and Comparison with Cytochrome P450 3A4 and Other Forms: Effects of Cytochrome P450–P450 and Cytochrome P450–b5Interactions
Hiroshi Yamazaki, Elizabeth M. J. Gillam, Mi‐Sook Dong, William W. Johnson, F. Peter Guengerich, Tsutomu Shimada
SJR Q1Archives of Biochemistry and Biophysics
PharmacologyPharmacology, Toxicology and Pharmaceutics
2
Review|86 citations·2015
Proton pump inhibitor use and risk of spontaneous bacterial peritonitis in cirrhotic patients: a systematic review and meta-analysis
Hongbin Xu, H.D. Wang, Chao Li, Shujun Ye, Mi‐Sook Dong, Qing Xia, A.Q. Zhang, Ke Pan, X. Ge, Jin Dong
SJR Q4Genetics and Molecular ResearchOA

We used a meta-analysis approach to investigate the association between proton pump inhibitor (PPI) use and risk of spontaneous bacterial peritonitis (SBP) in cirrhotic patients. We searched Ovid Medline, Embase, and the Cochrane Library to identify eligible studies. We included studies that compared cirrhotic patients who did or did not use PPIs. The primary outcome was SBP, and the secondary outcome was overall bacterial infection. Results were pooled using random-effect models. This process l

HepatologyMedicine
3
Article|76 citations·2012
Estrogenic/antiestrogenic activities of a Epimedium koreanum extract and its major components: in vitro and in vivo studies
Hyun Ku Kang, Yun-Ho Choi, Hyo-Suk Kwon, Sang-Bum Lee, Dong‐Hyun Kim, Chung Ki Sung, Young In Park, Mi‐Sook Dong
SJR Q1Food and Chemical Toxicology
PharmacologyPharmacology, Toxicology and Pharmaceutics
4
Article|75 citations·2012
Anti-inflammatory effects of (Z)-ligustilide through suppression of mitogen-activated protein kinases and nuclear factor-κB activation pathways
J.W. Chung, Ran Joo Choi, Eun‐Kyoung Seo, Joo‐Won Nam, Mi‐Sook Dong, Eun Myoung Shin, Lian Guo, Yeong Shik Kim
SJR Q1Archives of Pharmacal Research
Complementary and alternative medicineMedicine
5
Article|63 citations·2000
Phenotypes of flavin-containing monooxygenase activity determined by ranitidine N-oxidation are positively correlated with genotypes of linked FMO3 gene mutations in a Korean population
Ju‐Hee Kang, Woon‐Gye Chung, Kyung‐Hoon Lee, Chang‐Shin Park, Ju‐Seop Kang, Inchul Shin, Hyung‐Keun Roh, Mi‐Sook Dong, Hyun-Moon Baek, Young‐Nam Cha
Pharmacogenetics

A non-invasive urine analysis method to determine the in-vivo flavin-containing mono-oxygenase (FMO) activity catalysing N-oxidation of ranitidine (RA) was developed and used to phenotype a Korean population. FMO activity was assessed by the molar concentration ratio of RA and RANO in the bulked 8 h urine. This method was used to determine the FMO phenotypes of 210 Korean volunteers (173 men and 37 women, 110 nonsmokers and 100 smokers). Urinary RA/RANO ratio, representing the metabolic ratio an

PharmacologyPharmacology, Toxicology and Pharmaceutics
6
Article|55 citations·1995
Bioactivation of aromatic amines by recombinant human cytochrome P4501A2 expressed in Ames tester strain bacteria: a substitute for activation by mammalian tissue preparations.
P. David Josephy, Lillian S. DeBruin, H. Lord, Jeong-Ho Oak, David H. Evans, Zijian Guo, Mi‐Sook Dong, F. Peter Guengerich
PubMed

The most widely used bioassay in genetic toxicology is the Ames test, which combines a bacterial mutagenicity assay (reversion of Salmonella typhimurium histidine-auxotrophic tester strains) with an exogenous bioactivation system (hepatic postmitochondrial supernatant or "S9"). The enzymatic activities of S9 prepared from the tissues of experimental animals are difficult to control. We show that the requirement for S9 can be obviated by the engineered expression of enzymes of bioactivation withi

Cancer ResearchBiochemistry, Genetics and Molecular Biology
7
Article|49 citations·2005
Effects of 2,4-D and DCP on the DHT-Induced Androgenic Action in Human Prostate Cancer Cells
Hyun-Jung Kim, Young In Park, Mi‐Sook Dong
SJR Q1Toxicological SciencesOA

2,4-Dichlorophenoxyacetic acid (2,4-D) and its metabolite 2,4-dichlorophenol (DCP) are used extensively in agriculture as herbicides, and are suspected of potential endocrine disruptor activity. In a previous study, we showed that these compounds exhibited synergistic androgenic effects by co-treatment with testosterone in the Hershberger assay. To elucidate the mechanisms of the synergistic effects of these compounds on the androgenicity of testosterone, the androgenic action of 2,4-D and DCP w

Health, Toxicology and MutagenesisEnvironmental Science
8
Article|47 citations·2010
Identification of 2,3,6-trisubstituted quinoxaline derivatives as a Wnt2/β-catenin pathway inhibitor in non-small-cell lung cancer cell lines
Sang-Bum Lee, Young In Park, Mi‐Sook Dong, Young‐Dae Gong
SJR Q2Bioorganic & Medicinal Chemistry Letters
Organic ChemistryChemistry
9
Article|46 citations·2005
Effects of hydroxyl group numbers on the B-ring of 5,7-dihydroxyflavones on the differential inhibition of human CYP 1A and CYP1B1 enzymes
Hyunjung Kim, Sang Bum Lee, Song‐Kyu Park, Hwan Mook Kim, Young In Park, Mi‐Sook Dong
SJR Q1Archives of Pharmacal Research
PharmacologyPharmacology, Toxicology and Pharmaceutics
10
Article|40 citations·2004
Structure-related cytotoxicity and anti-hepatofibric effect of asiatic acid derivatives in rat hepatic stellate cell-line, HSC-T6
Mi‐Sook Dong, Seung-Hyun Jung, Hyun Jung Kim, Jeong‐Ran Kim, Longxuan Zhao, Eung-Seok Lee, Eunjoo H. Lee, Jung Bum Yi, Namkyu Lee, Yong-Baik Cho, Wie Jong Kwak, Young In Park
SJR Q1Archives of Pharmacal Research
Complementary and alternative medicineMedicine
11
Article|38 citations·2006
Comparison of prostate cancer cell lines for androgen receptor-mediated reporter gene assays
Hyun Jung Kim, Young In Park, Mi‐Sook Dong
SJR Q2Toxicology in Vitro
GeneticsBiochemistry, Genetics and Molecular Biology
12
Article|33 citations·2013
2,3,6-Trisubstituted quinoxaline derivative, a small molecule inhibitor of the Wnt/beta-catenin signaling pathway, suppresses cell proliferation and enhances radiosensitivity in A549/Wnt2 cells
Sang Bum Lee, Young‐Dae Gong, Young In Park, Mi‐Sook Dong
SJR Q2Biochemical and Biophysical Research Communications
Molecular BiologyBiochemistry, Genetics and Molecular Biology
13
Article|32 citations·1996
Identification of Retained N-Formylmethionine in Bacterial Recombinant Mammalian Cytochrome P450 Proteins with the N-Terminal Sequence MALLLAVFL...: Roles of Residues 3−5 in Retention and Membrane Topology
Mi‐Sook Dong, L. Chastine Bell, Zuyu Guo, Dennis Phillips, Ian A. Blair, F. Peter Guengerich
SJR Q1Biochemistry

An N-terminal block to Edman degradation was observed when any of five different mammalian cytochrome P450 (P450) proteins was expressed in Escherichia coli using the N-terminal sequence MALLLAVFL... This block was also seen in Salmonella typhimurium. With all proteins examined, the block could be removed by mild acid hydrolysis (0.6--6 N HCl, 23 degrees C) to expose Met as the N-terminus, suggesting N-formylMet retention. The N-terminal peptide of a modified P450 1A2 ("mutant 1", containing a t

BiochemistryBiochemistry, Genetics and Molecular Biology
14
Article|27 citations·2011
A novel 3-arylethynyl-substituted pyrido[2,3,-b]pyrazine derivatives and pharmacophore model as Wnt2/β-catenin pathway inhibitors in non-small-cell lung cancer cell lines
Young‐Dae Gong, Mi‐Sook Dong, Sang-Bum Lee, Nayeon Kim, Mi-Seon Bae, Nam-Sook Kang
SJR Q2Bioorganic & Medicinal Chemistry
Organic ChemistryChemistry
15
Article|24 citations·2008
Effects of CYP2C19 and MDR1 genotype on the eradication rate of Helicobacter pylori infection by triple therapy with pantoprazole, amoxycillin and clarithromycin
Jung Hwan Oh, Mi‐Sook Dong, Myung‐Gyu Choi, Hae‐Won Yoo, Sang‐Bum Lee, Young In Park, In‐Sik Chung
SJR Q1Journal of Gastroenterology and Hepatology

BACKGROUND: CYP2C19 polymorphism plays an important role in the metabolism of proton pump inhibitors. The multidrug resistance (MDR)1 genotype is associated with the successful eradication of Helicobacter pylori. The aim of the present study was to investigate the effects of CYP2C19 and MDR1 genotypes on the eradication rate of H. pylori using a pantoprazole-based triple therapy. METHODS: A total of 210 patients infected with H. pylori were treated with 40 mg pantoprazole, 500 mg clarithromycin

SurgeryMedicine

Research Areas

PharmacologyMolecular BiologyComplementary and alternative medicineHealth, Toxicology and MutagenesisSurgeryGenetics

Dive deeper into Misu Dong's research on Nubint

Open this lab's papers in the app to read with AI, summarize, and cite in your writing.