Publications by authors named "Ji-Hoon Cho"

Background: This study aimed to determine the risk of anterior cruciate ligament (ACL) injury in female college students according to sleep quality and use this information to prevent injury.

Methods: Twenty-six female university students were recruited for the present study. Participants underwent assessments for sleep quality, landing error scoring system (LESS), and electromyographic (EMG) activity for imbalances by comparing the muscle activity of the left and right rectus femoris (RF-to-RF) and biceps femoris (BF-to-BF) muscles.

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Heterobifunctional degraders (also known as proteolysis-targeting chimeras or PROTACs) have emerged in drug discovery as an alternative therapeutic modality for targeting disease-causing proteins that are challenging to modulate with standard protein inhibitors. Almost all current PROTACs under clinical studies use the E3 ligase cereblon (CRBN) to hijack the ubiquitin-proteasome system. In this study, we used high-throughput experimentation to identify new conditions to access carbon-carbon bonds on our CRBN warheads.

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Photoaffinity labeling (PAL) methodologies have proven to be instrumental for the unbiased deconvolution of protein-ligand binding events in physiologically relevant systems. However, like other chemical proteomic workflows, they are limited in many ways by time-intensive sample manipulations and data acquisition techniques. Here, we describe an approach to address this challenge through the innovation of a carboxylate bead-based protein cleanup procedure to remove excess small-molecule contaminants and couple it to plate-based, proteomic sample processing as a semiautomated solution.

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CYP3A5 is a cytochrome P450 (CYP) enzyme that metabolizes drugs and contributes to drug resistance in cancer. However, it remains unclear whether CYP3A5 directly influences cancer progression. In this report, we demonstrate that CYP3A5 regulates glucose metabolism in pancreatic ductal adenocarcinoma.

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Article Synopsis
  • Dysregulated pre-mRNA splicing and metabolism are key features of cancers driven by the MYC oncogene, and targeting these processes has potential for cancer therapy.
  • The study identifies JMJD6 as a central protein linking splicing and metabolism in MYC-driven neuroblastoma by interacting with RNA binding proteins and regulating specific glutaminase isoforms.
  • Additionally, JMJD6's role in the cancer cell response to the drug indisulam suggests it might be a promising target for developing treatments for MYC-driven cancers.
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Article Synopsis
  • Dysregulated pre-mRNA splicing and metabolism are key characteristics of MYC-driven cancers, with JMJD6 identified as a critical link between these processes in MYC-driven neuroblastoma.
  • JMJD6 collaborates with MYC and RNA binding proteins to regulate the alternative splicing of glutaminase isoforms, which are essential for cancer cell metabolism.
  • The study suggests targeting JMJD6 may be a promising therapeutic strategy for treating MYC-driven cancers, especially in conjunction with drugs like indisulam that hinder splicing factors affecting JMJD6.
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Article Synopsis
  • Researchers looked at a specific type of leukemia in kids, called KMT2Ar acute lymphoblastic leukemia (ALL), which has a low chance of recovery.
  • They tested 1,116 approved medicines and found that some can help fight this cancer by blocking certain cell processes.
  • When used on some patients who didn't respond to other treatments, 90% showed improvement, and this approach is now being tested in a new trial for infants with leukemia.
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Recent proteome and transcriptome profiling of Alzheimer's disease (AD) brains reveals RNA splicing dysfunction and U1 small nuclear ribonucleoprotein (snRNP) pathology containing U1-70K and its N-terminal 40-KDa fragment (N40K). Here we present a causative role of U1 snRNP dysfunction to neurodegeneration in primary neurons and transgenic mice (N40K-Tg), in which N40K expression exerts a dominant-negative effect to downregulate full-length U1-70K. N40K-Tg recapitulates N40K insolubility, erroneous splicing events, neuronal degeneration and cognitive impairment.

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Proteome profiling is a powerful tool in biological and biomedical studies, starting with samples at bulk, single-cell, or single-cell-type levels. Reliable methods for extracting specific cell-type proteomes are in need, especially for the cells (e.g.

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With recent advances in mass spectrometry-based proteomics technologies, deep profiling of hundreds of proteomes has become increasingly feasible. However, deriving biological insights from such valuable datasets is challenging. Here we introduce a systems biology-based software JUMPn, and its associated protocol to organize the proteome into protein co-expression clusters across samples and protein-protein interaction (PPI) networks connected by modules (e.

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The prevalence of metabolic syndrome (MetS) risk factors among the Korean population requires effective health surveillance and examination of the effects of preventative behaviors. Thus, the objective of this study is to evaluate the relationships between the clustering of MetS and MVPA in a large sample of 36,987 Koreans ranging from 20 to 80 years of age. This study recruited a total of 36,987 adults (23,813 males and 13,174 females).

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Recent advances in mass spectrometry (MS)-based proteomics allow the measurement of turnover rates of thousands of proteins using dynamic labeling methods, such as pulse stable isotope labeling by amino acids in cell culture (pSILAC). However, when applying the pSILAC strategy to multicellular animals (e.g.

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Background: The purpose of this study was to find the basic data of medical and exercise therapy by indexing lumbar extension muscle strength of low back pain (LBP) patients.

Methods: In this cross-sectional study, 3078 chronic LBP participants from The J hospital, Seoul, Republic of Korea, from 2003 to 2010 were enrolled. Maximum muscle strength was measured at maximum flexion angle and maximum extension angle according to range of motion (ROM) results.

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Isobaric tandem mass tag (TMT) labeling is widely used in proteomics because of its high multiplexing capacity and deep proteome coverage. Recently, an expanded 16-plex TMT method has been introduced, which further increases the throughput of proteomic studies. In this manuscript, we present an optimized protocol for 16-plex TMT-based deep-proteome profiling, including protein sample preparation, enzymatic digestion, TMT labeling reaction, two-dimensional reverse-phase liquid chromatography (LC/LC) fractionation, tandem mass spectrometry (MS/MS), and computational data processing.

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Background: Based on amyloid cascade and tau hypotheses, protein biomarkers of different Aβ and tau species in cerebrospinal fluid (CSF) and blood/plasma/serum have been examined to correlate with brain pathology. Recently, unbiased proteomic profiling of these human samples has been initiated to identify a large number of novel AD biomarker candidates, but it is challenging to define reliable candidates for subsequent large-scale validation.

Methods: We present a comprehensive strategy to identify biomarker candidates of high confidence by integrating multiple proteomes in AD, including cortex, CSF and serum.

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Background: Although sites and types of injury frequently occurring in fencers have been well described, the type of injury caused by the use of fencing movements is still unknown. This study aimed to provide basic data for injury prevention by understanding the sports injury status in fencers.

Methods: A total of 584 South Korean fencers were included in the survey and were classified according to the injured site, cause of injury, and movement that causes injury.

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