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Chul-hoon Kim

Yonsei University · Medicine

About the Lab

Professor Chul-hoon Kim's research lab focuses on the molecular mechanisms underlying neurodegenerative diseases and metabolic liver disorders, with a particular emphasis on the roles of metal ions—especially zinc—and signaling pathways in disease progression. The lab investigates how dysregulated protein phosphorylation, particularly through kinases like ERK and PKC, contributes to pathological changes in Alzheimer’s disease and nonalcoholic fatty liver disease (NAFLD). A central theme is the interplay between redox regulation, metal homeostasis, and transcription factor activation, such as NF-κB, in cellular stress and survival. The lab also explores the dual roles of antioxidants like pyrrolidine dithiocarbamate (PDTC) in both protection and cytotoxicity, depending on cellular context and metal availability.

zinc signalingtau phosphorylationNF-kappaB activationmetabolic liver diseaseprotein kinase regulation

Research Overview

Papers
199
Total Citations
6,529
Papers (5y)
39
Primary Field
Medicine

Research Output Trend

Figures are computed from collected data and may differ slightly.

Publications per year (5y)
39total
2022
2023
2024
2025
2026
Citations per year (5y)
171total
20222023202420252026

Selected Papers

15
1
Review|339 citations·2008
Nonalcoholic fatty liver disease: A manifestation of the metabolic syndrome
Chul Hoon Kim, Zobair M. Younossi
SJR Q2Cleveland Clinic Journal of Medicine

Nonalcoholic fatty liver disease (NAFLD) has become the most common form of liver disease, affecting 20% to 30% of the US population. Its clinical manifestations are usually absent or subtle, and it usually comes to medical attention incidentally when aminotransferase levels are found to be elevated or a radiographic study reveals that the liver is fatty. Primary NAFLD is now considered the hepatic manifestation of the metabolic syndrome. The pathogenesis is thought to be a multiple-hit process

EpidemiologyMedicine
2
Review|139 citations·2007
Metabotropic glutamate receptors: Phosphorylation and receptor signaling
Chul Hoon Kim, Jinu Lee, Jae‐Youn Lee, Katherine W. Roche
SJR Q2Journal of Neuroscience ResearchOA

Metabotropic glutamate receptors (mGluRs) play important roles in neurotransmission, neuronal development, synaptic plasticity, and neurological disorders. Recent studies have revealed a sophisticated interplay between mGluRs and protein kinases: activation of mGluRs regulates the activity of a number of kinases, and direct phosphorylation of mGluRs affects receptor signaling, trafficking, and desensitization. Here we review the emerging literature on mGluR phosphorylation, signaling, and synapt

Cellular and Molecular NeuroscienceNeuroscience
3
Article|130 citations·2015
mGluR5 in the nucleus accumbens is critical for promoting resilience to chronic stress
Sora Shin, Obin Kwon, Jee In Kang, Somin Kwon, Sora Oh, Jiwon Choi, Chul Hoon Kim, Dong Goo Kim
SJR Q1Nature NeuroscienceOA
Behavioral NeuroscienceNeuroscience
4
Review|86 citations·2003
Zinc-induced NF-κB inhibition can be modulated by changes in the intracellular metallothionein level
Chul Hoon Kim, Joo Hee Kim, Jinu Lee, Young Soo Ahn
SJR Q2Toxicology and Applied PharmacologyOA
Nutrition and DieteticsNursing
5
Article|83 citations·2005
Protein Kinase C Phosphorylation of the Metabotropic Glutamate ReceptormGluR5 on Serine 839 Regulates Ca2+Oscillations
Chul Hoon Kim, Stephanie Braud, John Isaac, Katherine W. Roche
SJR Q1Journal of Biological ChemistryOA

The activation of Group 1 metabotropic glutamate receptors, mGluR5 and mGluR1alpha, triggers intracellular calcium release; however, mGluR5 activation is unique in that it elicits Ca2+ oscillations. A short region of the mGluR5 C terminus is the critical determinant and differs from the analogous region of mGluR1alpha by a single amino acid residue, Thr-840, which is an aspartic acid (Asp-854) in mGluR1alpha. Previous studies show that mGluR5-elicited Ca2+ oscillations require protein kinase C (

Cellular and Molecular NeuroscienceNeuroscience
6
Article|78 citations·1999
Zinc is required in pyrrolidine dithiocarbamate inhibition of NF‐κB activation
Chul Hoon Kim, Joo Hee Kim, Chung Y. Hsu, Young Soo Ahn
SJR Q1FEBS LettersOA

Pyrrolidine dithiocarbamate (PDTC) is a potent inhibitor of nuclear factor kappa B (NF-kappaB) activation. PDTC inhibited basal NF-kappaB activity of endothelial cells. PDTC, however, failed to inhibit basal NF-kappaB activity after withdrawal of serum in the media, and the inhibitory effect of PDTC could be restored by addition of zinc. When various preparations of metal ion-EDTA were tested with PDTC in serum-containing media, only Zn-EDTA failed to block the inhibitory effect of PDTC. The dep

Cancer ResearchBiochemistry, Genetics and Molecular Biology
7
Article|73 citations·1999
Pyrithione, a Zinc Ionophore, Inhibits NF-κB Activation
Chul Hoon Kim, Joo Hee Kim, Seok Jun Moon, Kwang Chul Chung, Chung Y. Hsu, Jeong Taeg Seo, Young Soo Ahn
SJR Q2Biochemical and Biophysical Research CommunicationsOA
Cancer ResearchBiochemistry, Genetics and Molecular Biology
8
Article|61 citations·1999
Pyrrolidine Dithiocarbamate Induces Bovine Cerebral Endothelial Cell Death by Increasing the Intracellular Zinc Level
Chul Hoon Kim, Joo Hee Kim, Jan Xu, Chung Y. Hsu, Young Soo Ahn
SJR Q1Journal of NeurochemistryOA

The antioxidant and metal-chelating effects of pyrrolidine dithiocarbamate (PDTC) have been extensively studied. PDTC prevents cell death induced by various insults. However, PDTC itself may cause cell death in selected experimental paradigms. PDTC induced bovine cerebral endothelial cell death. However, in serum-depleted medium, PDTC did not affect the cell viability, suggesting that certain factors in serum may mediate the cytotoxic effect of PDTC. The metal chelators bathocuproine disulfonic

Nutrition and DieteticsNursing
9
Article|59 citations·2011
Zinc stimulates tau S214 phosphorylation by the activation of Raf/mitogen-activated protein kinase-kinase/extracellular signal-regulated kinase pathway
In‐Sook Kim, Eun Ji Park, Jeho Seo, Suk Jin Ko, Jinu Lee, Chul Hoon Kim
SJR Q3NeuroreportOA

Hyperphosphorylated tau is a main component of neurofibrillary tangles, a pathological hallmark of Alzheimer's disease (AD). There is evidence that various protein kinases are involved in tau hyperphosphorylation. However, little is known about AD-related stimuli that activates tau kinases. We investigated the role of zinc, a metal involved in AD pathology, in tau phosphorylation. Zinc increased the phosphorylation of serine 214 (S214) in tau protein in human wild-type tau1-441-expressing SH-SY5

PhysiologyMedicine
10
Article|49 citations·2009
Association of Common Type 2 Diabetes Risk Gene Variants and Posttransplantation Diabetes Mellitus in Renal Allograft Recipients in Korea
Eun Seok Kang, Myoung Soo Kim, Chul Hoon Kim, Chung Mo Nam, Seung Jin Han, Kyu Yeon Hur, Chul Woo Ahn, Bong Soo, Soon Il Kim, Hyun Chul Lee, Yu Seun Kim
SJR Q1TransplantationOA

These data suggest that genetic variations in TCF7L2, SLC30A8, HHEX, CDKAL1, CDKN2A/B, and KCNQ1 are associated with PTDM in Korea.

TransplantationMedicine
11
Article|47 citations·2016
A genetic variant in GLP1R is associated with response to DPP-4 inhibitors in patients with type 2 diabetes
Eugene Han, Hye Sun Park, Obin Kwon, Eun Yeong Choe, Hye Jin Wang, Yong‐ho Lee, Sang‐Hak Lee, Chul Hoon Kim, Lee-Kyung Kim, Soo Heon Kwak, Kyong Soo Park, Chul Sik Kim
SJR Q3MedicineOA

Incretin hormone-based therapy in type 2 diabetes has been widely used, and dipepdityl peptidase-4 (DPP-4) inhibitors, which prevent incretin degradation, have become popular oral hypoglycemic agents. The efficacy of DPP-4 inhibitors varies from individuals, and factors determining responses to DPP-4 inhibitors have not been fully established. We aimed to investigate whether genetic variations in glucagon-like peptide (GLP-1) receptor are associated with responses to DPP-4 inhibitors in patients

Endocrinology, Diabetes and MetabolismMedicine
12
Article|47 citations·2013
dTULP, the Drosophila melanogaster Homolog of Tubby, Regulates Transient Receptor Potential Channel Localization in Cilia
Jina Park, Jeongmi Lee, Jaewon Shim, Woongsu Han, Jinu Lee, Yong Chul Bae, Yun Doo Chung, Chul Hoon Kim, Seok Jun Moon
SJR Q1PLoS GeneticsOA

Mechanically gated ion channels convert sound into an electrical signal for the sense of hearing. In Drosophila melanogaster, several transient receptor potential (TRP) channels have been implicated to be involved in this process. TRPN (NompC) and TRPV (Inactive) channels are localized in the distal and proximal ciliary zones of auditory receptor neurons, respectively. This segregated ciliary localization suggests distinct roles in auditory transduction. However, the regulation of this localizat

Plant ScienceAgricultural and Biological Sciences
13
Article|46 citations·2017
Changes in brain metabolic connectivity underlie autistic-like social deficits in a rat model of autism spectrum disorder
Hojin Cho, Chul Hoon Kim, Elizabeth Quattrocki Knight, Hye-Won Oh, Bumhee Park, Dong Goo Kim, Hae‐Jeong Park
SJR Q1Scientific ReportsOA

Abstract The neurobiological basis of social dysfunction and the high male prevalence in autism spectrum disorder (ASD) remain poorly understood. Although network alterations presumably underlie the development of autistic-like behaviors, a clear pattern of connectivity differences specific to ASD has not yet emerged. Because the heterogeneous nature of ASD hinders investigations in human subjects, we explored brain connectivity in an etiologically homogenous rat model of ASD induced by exposure

Cognitive NeuroscienceNeuroscience
14
Article|44 citations·2010
A low-risk ZnT-8 allele (W325) for post-transplantation diabetes mellitus is protective against cyclosporin A-induced impairment of insulin secretion
I. Kim, Eun Seok Kang, Yesol Yim, Sung-Jea Ko, Jeong Sh, John Hoon Rim, Yu Seun Kim, Chul Woo Ahn, Bong Soo, H. C. Lee, Chul Hoon Kim
SJR Q2The Pharmacogenomics JournalOA
SurgeryMedicine
15
Article|37 citations·2015
Ciliary Phosphoinositide Regulates Ciliary Protein Trafficking in Drosophila
Jina Park, Nayoung Lee, Adriana Kavoussi, Jeong Taeg Seo, Chul Hoon Kim, Seok Jun Moon
SJR Q1Cell ReportsOA

Cilia are highly specialized antennae-like cellular organelles. Inositol polyphosphate 5-phosphatase E (INPP5E) converts PI(4,5)P2 into PI4P and is required for proper ciliary function. Although Inpp5e mutations are associated with ciliopathies in humans and mice, the precise molecular role INPP5E plays in cilia remains unclear. Here, we report that Drosophila INPP5E (dINPP5E) regulates ciliary protein trafficking by controlling the phosphoinositide composition of ciliary membranes. Mutations in

GeneticsBiochemistry, Genetics and Molecular Biology

Research Areas

Molecular BiologyCellular and Molecular NeurosciencePhysiologyGeneticsCancer ResearchSurgery

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