Publications by authors named "Dasom Hwang"

HPV/pap tests are widely used for cervical cancer screening, playing a crucial role in early diagnosis and guiding future treatment options. However, approximately 50% of cervical cancer patients are diagnosed at an advanced stage, which is associated with higher recurrence rates and poorer survival outcomes than early-stage diagnoses. This underscores the need for effective treatments for advanced-stage cervical cancer.

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Small molecules that exhibit broad-spectrum enteroviral inhibitory activity by targeting viral replication proteins are highly desired in antiviral drug discovery studies. To discover new human rhinovirus (hRV) inhibitors, we performed a high-throughput screening of 100,000 compounds from the Korea Chemical Bank library. This search led to identification of two phosphatidylinositol-4-kinase IIIβ (PI4KIIIβ) inhibitors having the pyrazolo-pyrimidine core structure, which display moderate anti-rhinoviral activity along with mild cytotoxicity.

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  • The text is a correction related to a published article, specifically identified by its DOI: 10.1039/D3MD00630A.
  • This correction aims to address errors or inaccuracies found in the original publication.
  • It emphasizes the importance of maintaining scientific integrity and ensuring that research findings are accurate and reliable.
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  • Human rhinoviruses (hRVs) cause respiratory infections and worsen conditions like asthma and COPD, with over 160 genetically diverse strains complicating treatment development.
  • Researchers discovered new inhibitors of the PI4KIIIβ enzyme, critical for viral replication, through high-throughput screening, with one compound, 7f, showing promising antiviral activity and low toxicity.
  • Inhibitor 7f demonstrates strong selectivity against hRVs and enteroviruses, making it a potential candidate for future antiviral therapies targeting hRVs.
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  • The study explores a nanotechnology approach to enhance the efficacy of remdesivir (RDS) as an antiviral treatment for SARS-CoV-2.
  • Researchers developed nanosized RDS-NLC, which improved the drug's effectiveness by increasing its bioavailability and cellular absorption.
  • The findings suggest that using NLC technology could be a promising strategy to enhance the antiviral properties of existing antiviral agents against SARS-CoV-2 and its variants.
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Background: Staphylococcus (S) aureus colonization is known to cause skin barrier disruption in atopic dermatitis (AD) patients. However, it has not been studied how S. aureus induces aberrant epidermal lipid composition and skin barrier dysfunction.

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Liquid biopsy has been emerging for early screening and treatment monitoring at each cancer stage. However, the current blood-based diagnostic tools in breast cancer have not been sufficient to understand patient-derived molecular features of aggressive tumors individually. Herein, we aimed to develop a blood test for the early detection of breast cancer with cost-effective and high-throughput considerations in order to combat the challenges associated with precision oncology using mRNA-based tests.

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MicroRNAs are reported as promising biomarkers for the diagnosis and treatment of breast cancer. miR-1260b is identified as a tumor-associated noncoding microRNA in other cancers, although the role of miR-1260b and its clinical relevance in breast cancer remain unclear. In this study, miR-1260b as a potential prognostic biomarker was observed by univariate and multivariate Cox regression analyses in 102 breast tumor tissues.

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  • - Researchers developed new compounds based on an existing antiviral to effectively inhibit human rhinovirus (hRV) replication and other enteroviruses.
  • - The most promising compound, 2c (KR-25210), demonstrated strong antiviral activity with a half-maximal effective concentration of ≤ 2 µM against various hRVs, while also showing good drug-like properties.
  • - Further studies indicated that compound 2c functions by targeting the virus replication stages, rather than inhibiting the viral capsid.
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The diagnosis and prognosis of tuberculosis remains challenging and necessitates the development of a new test that can accurately diagnose and monitor treatment responses. In this regard, miRNA is becoming a potential diagnostic and prognostic biomarker which differentiates treatment respondents from non-respondents for various non-infectious and infectious diseases, including tuberculosis. The concentration of miRNAs varies based on cell type, disease, and site of infection, implicating that selection of an optimal reference gene is crucial, and determines the quantification of transcript level and biological interpretation of the data.

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Tuberculosis infection exhibits different forms, namely, pulmonary, extrapulmonary, and latent. Here, diagnostic markers based on the gene expression of cytokines and chemokines for differentiating between tuberculosis infection state(s) were identified. Gene expression of seven cytokines (Interferon gamma (IFN-γ), Interferon gamma-induced protein 10 (IP-10), Interleukin-2 receptor (IL-2R), C-X-C Motif Chemokine Ligand 9 (CXCL-9), Interleukin 10 (IL-10), Interleukin 4 (IL-4), and Tumor Necrosis Factor alpha (TNF-α)) in response to tuberculosis antigen was analyzed using real-time polymerase reaction.

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: Breast cancer is the most common cancer among women worldwide. Early stage diagnosis is important for predicting increases in treatment success rates and decreases in patient mortality. Recently, circulating biomarkers such as circulating tumor cells, circulating tumor DNA, exosomes, and circulating microRNAs have been examined as blood-based markers for the diagnosis of breast cancer.

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Background: Although the incidence of tuberculosis (TB) is decreasing, cases of multidrug-resistant (MDR) TB and extensively drug-resistant (XDR) TB continue to increase. As conventional phenotype drug susceptibility testing (pDST) takes six to eight weeks, molecular assays are widely used to determine drug resistance. we developed QuantaMatrix Multiplexed Assay Platform (QMAP) MDR/XDR assay (QuantaMatrix Inc.

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