Dong‐Hyung Cho

ORCID: 0000-0002-8859-0310
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About
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Research Areas
  • Autophagy in Disease and Therapy
  • Mitochondrial Function and Pathology
  • Epigenetics and DNA Methylation
  • RNA modifications and cancer
  • Genetic and Kidney Cyst Diseases
  • Ferroptosis and cancer prognosis
  • Peroxisome Proliferator-Activated Receptors
  • Cancer-related gene regulation
  • melanin and skin pigmentation
  • Alzheimer's disease research and treatments
  • ATP Synthase and ATPases Research
  • Cancer-related molecular mechanisms research
  • Cell death mechanisms and regulation
  • RNA Research and Splicing
  • Genetic factors in colorectal cancer
  • Cancer, Hypoxia, and Metabolism
  • Cancer therapeutics and mechanisms
  • Glycosylation and Glycoproteins Research
  • Endoplasmic Reticulum Stress and Disease
  • Sulfur Compounds in Biology
  • DNA Repair Mechanisms
  • Calcium signaling and nucleotide metabolism
  • Ubiquitin and proteasome pathways
  • Sirtuins and Resveratrol in Medicine
  • Colorectal Cancer Treatments and Studies

Kyungpook National University
2018-2025

Suwon Research Institute
2025

Institute for Basic Science
2024

Kyung Hee University
2011-2021

Asan Medical Center
2008-2019

Kyung Hee University East-West Neo Medical Center
2014-2017

University of Ulsan
2008-2010

Sanford Burnham Prebys Medical Discovery Institute
2007-2010

Ulsan College
2008-2010

Gwangju Institute of Science and Technology
2004

Mitochondria continuously undergo two opposing processes, fission and fusion. The disruption of this dynamic equilibrium may herald cell injury or death contribute to developmental neurodegenerative disorders. Nitric oxide functions as a signaling molecule, but in excess it mediates neuronal injury, part via mitochondrial fragmentation. However, the underlying mechanism for nitric oxide–induced pathological remains unclear. We found that produced response β-amyloid protein, thought be key...

10.1126/science.1171091 article EN Science 2009-04-02

Excessive mitochondrial fission is a prominent early event and contributes to dysfunction, synaptic failure, neuronal cell death in the progression of Alzheimer's disease (AD). However, it remains be determined whether inhibition excessive beneficial mammal models AD. To determine dynamin-related protein 1 (Drp1), key regulator fragmentation, can disease-modifying therapeutic target for AD, we examined effects Drp1 inhibitor on dysfunctions induced by oligomeric amyloid-β (Aβ) neurons...

10.1523/jneurosci.2385-16.2017 article EN cc-by-nc-sa Journal of Neuroscience 2017-04-21

Peroxiredoxins (Prx), a family of peroxidases that reduce intracellular peroxides with the thioredoxin system as electron donor, are highly expressed in various cellular compartments. Among antioxidant Prx enzymes, Prx2 is most abundant mammalian neurons, making it prime candidate to defend against oxidative stress. Here we report S-nitrosylated (forming SNO-Prx2) by reaction nitric oxide at two critical cysteine residues (C51 and C172), preventing its peroxides. We observed increased...

10.1073/pnas.0705904104 article EN Proceedings of the National Academy of Sciences 2007-11-15

Colorectal cancer (CRC) patients frequently experience disease recurrence and distant metastasis. This study aimed to identify prognostic indicators, including individual responses chemotherapy, in CRC patients. RNA‐seq data was generated using 54 samples (normal colon, primary CRC, liver metastases) from 18 genes associated with aggressiveness were identified. A risk score based on these developed validated four independent patient cohorts ( n = 1063). Diverse statistical methods applied...

10.1016/j.molonc.2014.06.016 article EN other-oa Molecular Oncology 2014-07-04

We screened a chemical library in MCF-7 cells stably expressing green fluorescent protein (GFP)-conjugated microtubule-associated 1 light chain 3 (LC3) (GFP-LC3-MCF-7) using cell-based assay, and identified BIX-01294 (BIX), selective inhibitor of euchromatic histone-lysine N-methyltransferase 2 (EHMT2), as strong autophagy inducer. BIX enhanced formation GFP-LC3 puncta, LC3-II, free GFP, signifying autophagic activation. Inhibition these phenomena with chloroquine increasement punctate...

10.4161/auto.26308 article EN Autophagy 2013-12-05

Lysophagy eliminates damaged lysosomes and is crucial to cellular homeostasis; however, its underlying mechanisms are not entirely understood. We screen a ubiquitination-related compound library determine that the substrate recognition component of SCF-type E3 ubiquitin ligase complex, SCFFBXO3(FBXO3), which critical lysophagy regulator. Inhibition FBXO3 reduces lysophagic flux in response L-leucyl-L-leucine methyl ester (LLOMe). Furthermore, interacts with TMEM192, leading ubiquitination...

10.1038/s41467-025-56294-y article EN cc-by-nc-nd Nature Communications 2025-01-28

Background Autophagy has paradoxical and complex functions in cancer development, autophagy-related genes (ATG) are key regulators autophagy. Until now, more than 30 different ATG proteins have been identified yeast, their mammalian counterparts also reported. Although the roles of a few characterized, role ATG10 is almost completely unknown. Methodology/Principal Findings To investigate clinicopathological colorectal cancer, we analyzed expression tissues cell lines. Protein analysis showed...

10.1371/journal.pone.0052705 article EN cc-by PLoS ONE 2012-12-20

A primary cilium is an antenna-like structure on the cell surface that plays a crucial role in sensory perception and signal transduction. Mitochondria, 'powerhouse' of cell, control survival, death. The cellular ability to remove dysfunctional mitochondria through mitophagy important for survival. We show here mitochondrial stress, caused by respiratory complex inhibitors excessive fission, robustly stimulates ciliogenesis different types cells including neuronal cells. Mitochondrial...

10.1038/s41419-019-2184-y article EN cc-by Cell Death and Disease 2019-12-16

Mitochondrial quality control maintains mitochondrial function by regulating dynamics and mitophagy. Despite the identification of factors, little is known about crucial regulators coordinating both fission Through a cell-based functional screening assay, FK506 binding protein 8 (FKBP8) was identified to target microtubule-associated 1 light chain 3 (LC3) mitochondria change morphology. Microscopy analysis revealed that formation tubular enlarged observed in FKBP8 knockdown HeLa cells cortex...

10.1096/fj.201901735r article EN The FASEB Journal 2019-12-26

Peroxisomes are rapidly degraded during amino acid and oxygen deprivation by a type of selective autophagy called pexophagy. However, how damaged peroxisomes detected removed from the cell is poorly understood. Recent studies suggest that peroxisomal matrix protein import machinery may serve double duty as quality control machinery, where they directly involved in activating Here, we explored whether any factors required to prevent pexophagy, such their loss designates for degradation. Using...

10.1080/15548627.2022.2160566 article EN cc-by-nc-nd Autophagy 2022-12-21

Mitochondrial dynamics not only involves mitochondrial morphology but also biogenesis, distribution, and cell death. To identify specific regulators to mitochondria dynamics, we screened a chemical library identified niclosamide as potent inducer of fission. Niclosamide promoted fragmentation this was blocked by down-regulation Drp1. treatment resulted in the disruption membrane potential reduction ATP levels. Moreover, led apoptotic death caspase-3 activation. Interestingly, increased...

10.5483/bmbrep.2011.44.8.517 article EN cc-by-nc BMB Reports 2011-08-31

Objectives:To evaluate the association of microsatellite instability (MSI) with clinicopathologic features and oncologic outcomes in patients poorly differentiated colorectal cancer (PD).

10.1309/ajcp8p2dynkgrbvi article EN American Journal of Clinical Pathology 2013-08-16
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