Publications by authors named "Jisung Hwang"

Article Synopsis
  • Widespread interest in nanoscale pillar structures for optical devices faces challenges like high equipment costs and limited scalability due to traditional manufacturing methods.
  • The study introduces a novel technique using thermally assisted nanotransfer printing to create highly uniform nanoscale pillar arrays, achieving an impressive density of 0.1 tera-pillars per square inch.
  • These nanopillars are demonstrated as effective surface-enhanced Raman scattering sensors, providing consistent performance and sensitivity at very low concentrations while maintaining durability for multiple uses.
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  • Proteins inside living organisms can self-assemble into various 3D structures that serve specific functions, which can be used to create new materials through a process called biotemplating, though traditional methods face challenges in adaptability and functionality.* -
  • The study introduces CamBio, a new integrated biotemplating platform that labels target protein structures with antibodies and grows functional materials, allowing for better control over the nanostructure's properties and designed for advanced applications like surface-enhanced Raman spectroscopy (SERS).* -
  • CamBio not only generates plasmonic nanostructures for precise measurements but also enhances performance through iterative antibody labeling strategies, and demonstrates its practical applications with substrates made from cells and whole meat, which
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Coarse-grained (CG) interactions determined via bottom-up methodologies can faithfully reproduce the structural correlations observed in fine-grained (atomistic resolution) systems, yet they can suffer from limited extensibility due to complex many-body correlations. As part of an ongoing effort to understand and improve the applicability of bottom-up CG models, we propose an alternative approach to address both accuracy and transferability. Our main idea draws from classical perturbation theory to partition the hard sphere repulsive term from effective CG interactions.

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Estimating accurate radiation doses when a radioactive source's location is unknown can protect workers from radiation exposure. Unfortunately, depending on a detector's shape and directional response variations, conventional G(E) function can be prone to inaccurate dose estimations. Therefore, this study estimated accurate radiation doses regardless of source distributions, using the multiple G(E) function groups (i.

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We developed a multi-tasking deep learning model for simultaneous pulse height estimation and pulse shape discrimination for pile-up n/γ signals. Compared with single-tasking models, our model showed better spectral correction performance with higher recall for neutrons. Further, it achieved more stable neutron counting with less signal loss and a lower error rate in the predicted gamma ray spectra.

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Dose-rate monitoring instruments measure the ambient dose equivalent and hence are crucial for protecting workers from radiation exposure. Although plastic scintillation detectors (PSDs) are ideal equipment for dosimetry, they are rarely used owing to the lower detection efficiency than other scintillation detectors. In this study, we acquired ten types of G(E) functions to utilize a PSD in spectroscopic dosimetry using the least-square and first-order methods.

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We propose a Bayesian denoising method to improve the quality of ghost imaging. The proposed method achieved the highest PSNR and SSIM in both binary and gray-scale targets with fewer measurements. Experimentally, it obtained a reconstructed image of a USAF target where the PSNR and SSIM of the image were up to 12.

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Article Synopsis
  • Lutetium-based inorganic scintillators are gaining attention due to their beneficial physical properties, but they may have drawbacks stemming from naturally occurring radioisotopes in luetium.
  • Previous research mainly focused on specific interactions like the photoelectric effect, leaving other photon interactions less explored.
  • This study introduces a new method that combines various energy spectra from different radiation interactions, providing a more comprehensive analysis that aligns well with experimental results.
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  • - The study investigates the apoptotic mechanism of ginsenoside metabolite compound K in colorectal cancer cells, highlighting its superior ability to reduce cell viability and alter key protein expressions compared to control HCT116 cells.
  • - Through its effects, compound K was shown to increase sub G1 cell population and decrease levels of proteins associated with survival and proliferation, including LGR5, c-Myc, and procaspase3.
  • - Additionally, compound K enhances the effectiveness of traditional chemotherapy drugs like 5-fluorouracil and Doxorubicin, suggesting its potential for combined therapy in treating colorectal cancer by inhibiting LGR5 through a caspase and p53 dependent mechanism.
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Though limited success through chemotherapy, radiotherapy and surgery has been obtained for efficient cancer therapy for modern decades, cancers are still considered high burden to human health worldwide to date. Recently repurposing drugs are attractive with lower cost and shorter time compared to classical drug discovery, just as Metformin from Galega officinalis, originally approved for treating Type 2 diabetes by FDA, is globally valued at millions of US dollars for cancer therapy. As most previous reviews focused on FDA approved drugs and synthetic agents, current review discussed the anticancer potential of phytochemicals originally approved for treatment of cardiovascular diseases, diabetes, infectious diarrhea, depression and malaria with their molecular mechanisms and efficacies and suggested future research perspectives.

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Though Forkhead box P (FOXP) transcription factors comprising of FOXP1, FOXP2, FOXP3 and FOXP4 are involved in the embryonic development, immune disorders and cancer progression, the underlying function of FOXP3 targeting CD4 + CD25+ regulatory T (Treg) cells and the dual roles of FOXP proteins as an oncogene or a tumor suppressor are unclear and controversial in cancers to date. Thus, the present review highlighted research history, dual roles of FOXP proteins as a tumor suppressor or an oncogene, their molecular networks with other proteins and noncoding RNAs, cellular immunotherapy targeting FOXP3, and clinical implications in cancer progression.

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In the current study, the function of long noncoding RNA (LncRNA) RAB5IF was elucidated in hepatocellular carcinoma (HCCs) in association with LGR5 related signaling. Here TCGA analysis revealed that LncRNA RAB5IF was overexpressed in HCC, and its overexpression level was significantly ( < 0.05) correlated with poor prognosis in patients with HCC.

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Though Atorvastatin has been used as a hypolipidemic agent, its anticancer mechanisms for repurposing are not fully understood so far. Thus, in the current study, its apoptotic and autophagic mechanisms were investigated in non-small cell lung cancers (NSCLCs). Atorvastatin increased cytotoxicity, sub G1 population, the number of apoptotic bodies, cleaved poly (ADP-ribose) polymerase (PARP) and caspase 3 and activated p53 in H1299, H596, and H460 cells.

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Use of femoral-femoral veno-arterial (VA) extracorporeal membrane oxygenation (ECMO) for cardiopulmonary support during lung transplantation can be inadequate for efficient distribution of oxygenated blood into the coronary circulation. We hypothesized that creating a left-to-right shunt flow using veno-arterio-venous (VAV) ECMO would alleviate the differential hypoxia. Total 10 patients undergoing lung transplantation were enrolled in this study.

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As p300-mediated RelA/p65 hyperacetylation by signal transducers and activators of transcription 3 (STAT3) is critical for NF-κB activation, in the current study, the apoptotic mechanism of lambertianic acid (LA) was explored in relation to STAT3 phosphorylation and RelA/p65 acetylation in MCF-7, DU145, PC-3, and MDA-MB-453 cells. LA significantly increased the cytotoxicity, sub G 1 population, and the cleavage of poly (ADP-ribose) polymerase (PARP) in MDA-MB-453 or PC-3 cells (STAT3 mutant), more than in the MCF-7 or DU145 cells (STAT3 wild). Consistently, LA inhibited the phosphorylation of STAT3 and nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB), and disrupted the interaction between p-STAT3, p300, NF-κB, and RelA/p65 acetylation (Ac-RelA/p65) in the MCF-7 and DU145 cells.

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Background: Dexamethasone is widely used in cancer patients despite the concern that perioperative glucocorticoids may potentially cause immunosuppression. However, studies on the influence of dexamethasone on cancer recurrence after curative surgery have produced conflicting results. The goal of our study was to compare postoperative recurrence-free survival and overall survival between patients with breast cancer who received perioperative dexamethasone and those who did not.

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Although Moracin D derived from was known to have anti-inflammatory and antioxidant activities, the underlying antitumor mechanism of Moracin D has not been unveiled thus far. Thus, in the recent study, the apoptotic mechanism of Moracin D was elucidated in breast cancer cells. Herein, Moracin D exerted significant cytotoxicity in MDA-MB-231 and MCF-7 cells.

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Though melatonin is known to improve ultraviolet B (UVB)-induced oxidative damage and inflammatory conditions via the blockade of the nuclear factor (NF)-κB, interleukin (IL)-6, there is no report on the anti-wrinkle effect of melatonin to date. Hence in the present study, the anti-wrinkle mechanism of melatonin was elucidated in UVB treated HaCaT keratinocytes and hairless mice. Herein melatonin protected against a radical initiator tert-Butyl hydroperoxide (t-BOOH) induced reactive oxygen species (ROS) production, matrix metalloprotease 1 (MMP-1), pro-collagen and cytotoxicity in HaCaT keratinocytes.

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Lambertianic acid (LA) is a biologically active compound from the leaves of In the present study, apoptotic mechanisms of LA plus TNF-related apoptosis-inducing ligand (TRAIL) were elucidated in non-small cell lung cancer cells (NSCLCs). Cytotoxicity assay, flow cytometry, immunoprecipitation, and Western blotting were performed. Here, combined treatment of LA and TRAIL increased cytotoxicity, sub-G1 population, cleaved poly (ADP-ribose) polymerase (PARP), and caspase3/8/9 in A549 and H1299 cells compared to LA or TRAIL alone.

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