870 research outputs found
Liquid Communication: An Analysis of the Impact of Mobile Micro-blogging on Communication and Decision-Making
One of the most common forms of using mobile and social media technologies is the use of micro-blogging such as Twitter on mobile devices. The ubiquity of mobile devices combined with the communication via social network service like Twitter can potentially host a number of significant changes in the way people communicate and make decisions in a group setting. Yet, there is no theoretical framework that can effectively predict or interpret the changes. Based on the Bauman’s ‘liquid modernity,’ we develop a new concept, ‘communication liquidity’ which illustrates the extent to which communication is dynamic. The communication liquidity consists of the three dimensions – temporal, spatial, and conversational. We posit that micro-blogging on a mobile device brings higher levels of the communication liquidity in these three dimensions, which in turn improve the outcomes of communication among the group members
Sleep state classification using power spectral density and residual neural network with multichannel EEG signals.
This paper proposes a classification framework for automatic sleep stage detection in both male and female human subjects by analyzing the electroencephalogram (EEG) data of polysomnography (PSG) recorded for three regions of the human brain, i.e., the pre-frontal, central, and occipital lobes. Without considering any artifact removal approach, the residual neural network (ResNet) architecture is used to automatically learn the distinctive features of different sleep stages from the power spectral density (PSD) of the raw EEG data. The residual block of the ResNet learns the intrinsic features of different sleep stages from the EEG data while avoiding the vanishing gradient problem. The proposed approach is validated using the sleep dataset of the Dreams database, which comprises of EEG signals for 20 healthy human subjects, 16 female and 4 male. Our experimental results demonstrate the effectiveness of the ResNet based approach in identifying different sleep stages in both female and male subjects compared to state-of-the-art methods with classification accuracies of 87.8% and 83.7%, respectively
Phlegmonous Enteritis in a Patient with Congestive Heart Failure and Colon Cancer
Phlegmonous enteritis is a rare infective inflammatory disease of the intestine, predominantly involving the submucosal layer. It is difficult to diagnose and often fatal. Its association with alcoholism and various liver diseases, although rarely reported, is well documented. We report a case of phlegmonous enteritis in a male patient with congestive heart failure and colon cancer, and describe the ultrasonographic and CT findings
Prostate Cancer with Solitary Metastases to the Bilateral Testis
We present the case of an 81-year-old patient with testicular metastasis from prostate carcinoma. After the initial diagnosis of prostate cancer, he had an 8-year course of hormonal therapy and showed no clinical evidence of metastasis to other organs. Asymptomatic metastasis of prostate carcinoma to the testis is a rare clinical condition. We diagnosed his condition, based on histopathology following a subcapsular orchiectomy and transurethral resection of the prostate
Loss of Human Leukocyte Antigen Class I Expression Is Associated with Poor Prognosis in Patients with Advanced Breast Cancer
Background Human leukocyte antigen class I (HLA-I) molecules play important roles in regulating immune responses. Loss or reduction of HLA-I expression has been shown to be associated with prognosis in several cancers. Regulatory T-cells (Tregs) also play critical functions in immune response regulation. Evaluation of HLA-I expression status by the EMR8-5 antibody and its clinical impact in breast cancer have not been well studied, and its relationship with Tregs remains unclear. Methods We evaluated HLA-I expression and Treg infiltration by immunohistochemistry in 465 surgically resected breast cancer samples. We examined the correlation between HLA-I expression and Treg infiltration and clinicopathologic characteristics and survival analyses were performed. Results Total loss of HLA-I expression was found in 84 breast cancer samples (18.1%). Univariate survival analysis revealed that loss of HLA-I expression was significantly associated with worse disease-specific survival (DSS) (p = .029). HLA-I was not an independent prognostic factor in the entire patient group, but it was an adverse independent prognostic factor for DSS in patients with advanced disease (stage II–IV) (p = .031). Treg numbers were significantly higher in the intratumoral stroma of HLA-I–positive tumors than in HLA-I–negative tumors (median 6.3 cells/high power field vs 2.1 cells/high power field, p < .001). However, Tregs were not an independent prognostic factor in our cohort. Conclusions Our findings suggest that the loss of HLA-I expression is associated with poor prognosis in breast cancer patients, highlighting the role of HLA-I alterations in immune evasion mechanisms of breast cancer. HLA-I could be a promising marker that enables the application of more effective and precise immunotherapies for patients with advanced breast cancer
Polarization-selective vortex-core switching by orthogonal Gaussian-pulse currents
We experimentally demonstrate low-power-consumption vortex-core switching in
magnetic nanodisks using tailored rotating magnetic fields that are produced
with orthogonal and unipolar Gaussian-pulse currents. Optimal width of the
orthogonal pulses and their time delay are found to be determined only by the
angular eigenfrequency {\omega}_D for a given vortex-state disk of its
polarization p, such that {\sigma} = 1/{\omega}_D and {\Delta}t =
{\pi}p/2{\omega}_D, as studied from analytical and micromagnetic numerical
calculations. The estimated optimal pulse parameters are in good agreements
with the experimentally found results. This work provides a foundation for
energy-efficient information recording in vortex-core cross-point architecture.Comment: 32 pages, 10 figure
Mannosylated-serum albumin nanoparticle imaging to monitor tumor-associated macrophages under anti-PD1 treatment
Background
Immune checkpoint inhibitors such as anti-programmed cell death protein 1 (PD1) block tumor growth
by reinvigorating the immune system; however, determining their efcacy only by the changes in tumor size may
prove inaccurate. As the immune cells including macrophages in the tumor microenvironment (TME) are associ‑
ated with the response to anti-PD1 therapy, tumor-associated macrophages (TAMs) imaging using nanoparticles can
noninvasively provide the immune enrichment status of TME. Herein, the mannosylated-serum albumin (MSA) nano‑
particle was labeled with radioactive isotope 68Ga to target the mannose receptors on macrophages for noninvasive
monitoring of the TME according to anti-PD1 therapy.
Results
B16F10-Luc and MC38-Luc tumor-bearing mice were treated with anti-PD1, and the response to anti-PD1
was determined by the tumor volume. According to the fow cytometry, the responders to anti-PD1 showed an
increased proportion of TAMs, as well as lymphocytes, and the most enriched immune cell population in the TME
was also TAMs. For noninvasive imaging of TAMs as a surrogate of immune cell augmentation in the TME via anti-PD1,
we acquired [
68Ga] Ga-MSA positron emission tomography. According to the imaging study, an increased number of
TAMs in responders at the early phase of anti-PD1 treatment was observed in both B16F10-Luc and MC38-Luc tumorbearing mice models.
Conclusion
As representative immune cells in the TME, non-invasive imaging of TAMs using MSA nanoparticles can
refect the immune cell enrichment status in the TME closely associated with the response to anti-PD1. As non-inva‑
sive imaging using MSA nanoparticles, this approach shows a potential to monitor and evaluate anti-tumor response
to immune checkpoint inhibitors.This research was supported by the Basic Science Research Program through
the National Research Foundation of Korea (NRF), funded by the Ministry of
Education (NRF-2020R1A6A3A13069409), the Korean government the Ministry
of Science, ICT and Future Planning (2020R1A2C2010202, 2020R1A4A2002903,
2020M3A9B6038086, 2021M2E7A2079570, 2021R1A2C3009427,
2022M3E5F2018261), and the Ministry of Health and Welfare (HI19C0339,
HN22C0644). This study also was carried out by the research fund supported
by the fund project of Park Yang Sook - Chung Yung Ho in Seoul National
University
Impact of Nicotine Exposure on Hair Cell Toxicity and Embryotoxicity During Zebrafish Development
Objectives Nicotine has various adverse effects including negative impacts associated with maternal exposure. In the current study, we examined nicotine-induced damage of hair cells and embryotoxicity during zebrafish development. Methods Zebrafish embryos were exposed to nicotine at several concentrations (5, 10, 20, and 40 μM) and embryotoxicity were evaluated at 72 hours, including hatching rate, mortality, teratogenicity rate, and heart rate. Hair cells within the supraorbital (SO1 and SO2), otic (O1), and occipital (OC1) neuromasts were identified at 120 hours. Apoptosis and mitochondrial damage of hair cells were analyzed using TUNEL (terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end labeling) and DASPEI (2-[4-(dimethylamino)styryl]-N-ethylpyridinium iodide) assays, respectively, and changes of ultrastructure were observed by scanning electron microscopy. Results The control group without nicotine appeared normal with overall mortality and teratogenicity rate <5%. The hatching rate and mortality rate was not significantly different according to nicotine concentration (n=400 each). The abnormal morphology rate (n=400) increased and heart rate (n=150) decreased with increasing nicotine concentration (P<0.05). Nicotine-induced hair cell damage significantly increased as nicotine concentration increased. A significantly greater number of TUNEL-positive cells (P<0.01) and markedly smaller DASPEI area (P<0.01) were shown as nicotine concentration increased. Conclusion The current results suggest that nicotine induces dose-dependent hair cell toxicity in embryos by promoting apoptosis and mitochondrial and structural damage
Neuronal Apoptosis Inhibitory Protein is Overexpressed in Patients with Unfavorable Prognostic Factors in Breast Cancer
Neuronal apoptosis inhibitory protein (NAIP) is a recently identified inhibitor of apoptosis protein. However, the clinical relevance of NAIP expression is not completely understood. In an attempt to determine the clinical relevance of NAIP expression in breast cancer, the levels of NAIP and survivin expression were measured in 117 breast cancer samples and 10 normal breast tissues using quantitative reverse-transcriptase-polymerase chain reaction. While there was no evidence of NAIP expression in the normal breast tissue, NAIP was expressed in all breast cancer samples. The level of NAIP expression in breast cancer was significantly higher (257 times) than in the universal tumor control. There was a strong correlation between the level of NAIP expression and the level of survivin expression (p=0.001). The level of NAIP expression in patients with a large tumor (≥T2) and patients with an unfavorable histology (nuclear grade III) was significantly higher than in those patients with a small tumor (T1) and patients with a favorable histology (nuclear grade I, II) (p=0.026 and p=0.050, respectively). Although the level of NAIP expression was higher in patients with other unfavorable prognostic factors, it was not significant. The three-year relapse-free survival rate was not significantly the patients showing high NAIP expression and patients showing low NAIP expression (86.47±4.79% vs. 78.74±6.57%). Further studies should include the expressions of NAIP in a larger number of patients and for a longer period of follow-up to evaluate correlation with metastasis and treatment outcome. In conclusion, NAIP is overexpressed in breast cancer patients with unfavorable clinical features such as stage and tumor size, suggesting that NAIP would play a role in the disease manifestation
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