Publications by authors named "Chang-Woo Han"

Lactate dehydrogenase A (LDHA) is a key enzyme in Warburg's effect, a characteristic of cancer cells. LDHA is a target of anticancer agents that inhibit the metabolism of cancer cells. Gossypol is a known cancer therapeutic agent that inhibits LDHA by competitive inhibition.

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The tumor suppressor p53 plays important roles in suppressing the development and progression of cancer by responding to various stress signals. In addition, p53 can regulate the metabolic pathways of cancer cells by regulating energy metabolism and oxidative phosphorylation. Here, we present a mechanism for the interaction between p53 and ZNF568.

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The folate metabolism enzyme ALDH1L1 catalyzed 10-formyltetrahydrofolate to tetrahydrofolate and CO. Non-small cell lung cancer cells (NSCLC) strongly express ALDH1L1. Gossypol binds to an allosteric site and disrupts the folate metabolism by preventing NADP binding.

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Influenza A virus is the cause of a widespread human disease with high morbidity and mortality rates. The influenza virus encodes non-structural protein 1 (NS1), an exceedingly multifunctional virulence component. NS1 plays essential roles in viral replication and evasion of the cellular innate immune system.

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T-cell immunoglobulin and mucin protein 3 (Tim-3), also known as Hepatitis A virus cellular receptor 2, has been discovered to have a negative regulatory effect on murine T-cell responses. Galectin-9 exhibits various biological effects, including cell aggregation, eosinophil chemoattraction, activation, and apoptosis, observed in murine thymocytes, T-cells, and human melanoma cells. Such approach demonstrated that Galectin-9 acts as a binding partner on Tim-3 and mediates the T-cell inhibitory effects.

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E3L (RNA-binding protein E3) is one of the key IFN resistance genes encoded by VV and consists of 190 amino acids with a highly conserved carboxy-terminal double-stranded RNA-binding domain (dsRBD). PKR (dsRNA-dependent protein kinase) is an IFN-induced protein involved in anti-cell and antiviral activity. PKR inhibits the initiation of translation through alpha subunit of the initiation factor eIF2 (eIF2α) and mediates several transcription factors such as NF-κB, p53 or STATs.

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KRAS mutations occur in a quarter of all human cancers. When activated in its GTP-bound form, RAS stimulates diverse cellular systems, such as cell division, differentiation, growth, and apoptosis through the activations of various signaling pathways, which include mitogen-activated protein kinase (MAPK), phosphoinositide 3 kinases (PI3K), and RAL-GEFs pathways. We found that GJ101 (LYDVA) binds directly to the KRAS mutant (G12V) and showed tumor-suppressive activity.

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Fas-associated death domain (FADD) is an adapter molecule that bridges the interaction between receptor-interacting protein 1 (RIP1) and aspartate-specific cysteine protease-8 (caspase-8). As the primary mediator of apoptotic cell death, caspase-8 has two N-terminal death-effector domains (DEDs) and it interacts with other proteins in the DED subfamily through several conserved residues. In the tumor necrosis receptor-1 (TNFR-1)-dependent signaling pathway, apoptosis is triggered by the caspase-8/FADD complex by stimulating receptor internalization.

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Purpose: We aimed to investigate the association between air pollution concentration levels and hospital admissions for heart failure (HF) among older adults in metropolitan cities in South Korea.

Methods: We used hospital admission data of 1.8 million older adults in seven metropolitan cities from 2008 to 2016, derived from the National Health Insurance Service of South Korea.

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The KRAS oncogene is mutated in approximately ~30% of human cancers, and the targeting of KRAS has long been highlighted in many studies. Nevertheless, attempts to target KRAS directly have been ineffective. This review provides an overview of the structure of KRAS and its characteristic signaling pathways.

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PUMA (p53-upregulated modulator of apoptosis) is localized in mitochondria and a direct target in p53-mediated apoptosis. p53 elicits mitochondrial apoptosis via transcription-dependent and independent mechanisms. p53 is known to induce apoptosis via the transcriptional induction of PUMA, which encodes proapoptotic BH3-only members of the Bcl-2 protein family.

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Rationale: Although an association of fine particulate matter (PM) with asthma incidence has been assumed, there is insufficient evidence regarding the effect of long-term exposure to PM on incident asthma among elderly adults.

Objectives: This study aimed to investigate an association between long-term exposure to PM and incident asthma among elderly adults in South Korea.

Methods: Adults ≥65 years of age (n = 1,220,645) who did not visit hospitals for asthma during a washout period (between 2008 and 2010) were followed up until 2016 using data from the National Health Insurance System in South Korea.

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Article Synopsis
  • Most cancer cells rely on glycolysis and lactic acid fermentation for energy, even when oxygen is available, with PDK1 being a key enzyme often overexpressed in tumors and a target for colorectal cancer therapy.
  • Hemistepsin A (HsA), derived from Hemistepta lyrata, has been identified as a PDK1 inhibitor that can effectively reduce colorectal cancer growth and activate a specific cell death pathway.
  • HsA works by binding to PDK1, inhibiting its function, resulting in decreased lactate production, increased oxygen consumption, and promoting cancer cell apoptosis, suggesting its potential as a new anti-cancer drug.
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The Medical Information Department of a pharmaceutical manufacturer provides written scientific responses to unsolicited requests from healthcare providers for information on products that extends beyond the product labeling (off-label). These scientific response documents are non-promotional, evidence-based, and scientifically balanced, conforming with internal pharmaceutical manufacturer's procedures and the Food and Drug Administration (FDA) Draft Guidance on Responding to Unsolicited Requests for Off-Label Information. Members of phactMI™ developed this proposal to offer best practices for content generation of scientific response documents.

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In cancer cells, aerobic glycolysis rather than oxidative phosphorylation (OxPhos) is generally preferred for the production of ATP. In many cancers, highly expressed pyruvate dehydrogenase kinase 1 (PDK1) reduces the activity of pyruvate dehydrogenase (PDH) by inducing the phosphorylation of its E1α subunit (PDHA1) and subsequently, shifts the energy metabolism from OxPhos to aerobic glycolysis. Thus, PDK1 has been regarded as a target for anticancer treatment.

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Kirsten-RAS (KRAS) has been the target of drugs because it is the most mutated gene in human cancers. Because of the low affinity of drugs for KRAS mutations, it was difficult to target these tumor genes directly. We found a direct interaction between KRAS G12V and tumor suppressor novel H-REV107 peptide with high binding affinity.

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Article Synopsis
  • * Researchers identified a synthetic disaccharide called 6'-sialylgalactose (6SG) that strongly binds to VEGFR-2 and successfully inhibits abnormal angiogenesis without harming the cells.
  • * In experiments, 6SG not only reduced angiogenesis in human endothelial cells but also showed promise in reducing retinal and tumor angiogenesis in mouse models, suggesting it could be a useful treatment for conditions like retinopathy and cancer.
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  • Lactate dehydrogenase A (LDHA) is crucial for energy metabolism and cancer growth, and its inhibition can hinder cancer progression.
  • Machilin A (MA) acts as a competitive inhibitor of LDHA, effectively reducing cancer cell growth, lactate production, and overall survival in various types of cancer.
  • In mouse models, MA treatment led to significant tumor growth suppression and inhibited neovascularization by altering macrophage polarization, showcasing its potential as a cancer treatment.
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The influenza A virus is a highly infectious respiratory pathogen that sickens many people with respiratory disease annually. To prevent outbreaks of this viral infection, an understanding of the characteristics of virus-host interaction and development of an anti-viral agent is urgently needed. The influenza A virus can infect mammalian species including humans, pigs, horses and seals.

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  • Aerobic glycolysis is crucial for many tumors, and pyruvate dehydrogenase kinase (PDHK) is a key player by regulating this process, making it a target for cancer therapies.
  • The compound huzhangoside A (Hu.A), derived from certain plants, effectively inhibits PDHK, leading to reduced viability in various cancer cell lines, including breast and colon cancer.
  • Hu.A enhances oxygen consumption and reduces lactate levels in cancer cells, induces mitochondrial stress, and shows potential in curbing tumor growth in mice models.
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  • The Warburg effect is a phenomenon where cancer cells favor glycolysis over oxidative phosphorylation, making lactate dehydrogenase A (LDHA) a key target in anti-cancer drug development.
  • Recent research discovered that several selenobenzene compounds inhibit LDHA activity, with 1-(phenylseleno)-4-(trifluoromethyl) benzene (PSTMB) showing the strongest effect.
  • PSTMB not only inhibits LDHA activity and lactate production in various tumor cell lines but also triggers apoptosis in HT29 colon cancer cells, indicating its potential as a new anti-cancer drug targeting cancer metabolism.
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Hominis placenta (HP), a dried human placenta, has been known to target liver, lung, or kidney meridians, improving the functions associated with these meridians in traditional Chinese or Asian medicine (TCM). Since recent studies implicate an HP extract in suppressing inflammation, we investigated whether an aqueous HP extract can ameliorate inflammation that occurred in the lungs. When administered with a single intratracheal lipopolysaccharide (LPS), C57BL/6 mice developed an acute neutrophilic lung inflammation along with an increased expression of pro-inflammatory cytokine genes.

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Bojungikki-tang (BT), an Asian herbal remedy, has been prescribed to increase the vitality of debilitated patients. Since a compromised, weakened vitality often leads to illness, BT has been widely used to treat various diseases. However, little is known about the mechanism by which BT exerts its effect.

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Ras proteins are small GTPases that serve as master moderators of a large number of signaling pathways involved in various cellular processes. Activating mutations in Ras are found in about one-third of cancers. H-REV107, a K-Ras binding protein, plays an important role in determining K-Ras function.

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