4,557 research outputs found

    Impact of Human Immunodeficiency Virus in the Pathogenesis and Outcome of Patients with Glioblastoma Multiforme.

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    BackgroundImprovement in antiviral therapies have been accompanied by an increased frequency of non-Acquired Immune Deficiency Syndrome (AIDS) defining malignancies, such as glioblastoma multiforme. Here, we investigated all reported cases of human immunodeficiency virus (HIV)-positive patients with glioblastoma and evaluated their clinical outcomes. A comprehensive review of the molecular pathogenetic mechanisms underlying glioblastoma development in the setting of HIV/AIDS is provided.MethodsWe performed a PubMed search using keywords "HIV glioma" AND "glioblastoma," and "AIDS glioma" AND "glioblastoma." Case reports and series describing HIV-positive patients with glioblastoma (histologically-proven World Health Organization grade IV astrocytoma) and reporting on HAART treatment status, clinical follow-up, and overall survival (OS), were included for the purposes of quantitative synthesis. Patients without clinical follow-up data or OS were excluded. Remaining articles were assessed for data extraction eligibility.ResultsA total of 17 patients met our inclusion criteria. Of these patients, 14 (82.4%) were male and 3 (17.6%) were female, with a mean age of 39.5±9.2 years (range 19-60 years). Average CD4 count at diagnosis of glioblastoma was 358.9±193.4 cells/mm3. Tumor progression rather than AIDS-associated complications dictated patient survival. There was a trend towards increased median survival with HAART treatment (12.0 vs 7.5 months, p=0.10).ConclusionOur data suggests that HAART is associated with improved survival in patients with HIV-associated glioblastoma, although the precise mechanisms underlying this improvement remain unclear

    Landau Collision Integral Solver with Adaptive Mesh Refinement on Emerging Architectures

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    The Landau collision integral is an accurate model for the small-angle dominated Coulomb collisions in fusion plasmas. We investigate a high order accurate, fully conservative, finite element discretization of the nonlinear multi-species Landau integral with adaptive mesh refinement using the PETSc library (www.mcs.anl.gov/petsc). We develop algorithms and techniques to efficiently utilize emerging architectures with an approach that minimizes memory usage and movement and is suitable for vector processing. The Landau collision integral is vectorized with Intel AVX-512 intrinsics and the solver sustains as much as 22% of the theoretical peak flop rate of the Second Generation Intel Xeon Phi, Knights Landing, processor

    Optical control over transmission of terahertz radiation through arrays of subwavelength holes of varying size

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    Thomas Henry Isaac, J. Gómez Rivas, and Euan Hendry, Physical Review B, Vol. 80, article 193412 (2009). "Copyright © 2009 by the American Physical Society."We modulate the transmission of terahertz (THz) radiation through periodic arrays of subwavelength holes in a metallic film by using pulses of visible-wavelength light to photoexcite the semiconducting substrate of the hole arrays. By varying the photodoping level of the semiconductor we are able to switch off the resonant transmission of THz radiation through the array. By varying the size of the holes, we demonstrate the crucial role that surface modes play in the resonant transmission and ultimately in the photomodulation behavior of these structures. We demonstrate that the surface-wave transmission mechanism can allow for very efficient optical modulation of radiation transmission

    Rapamycin inhibits ALDH activity, resistance to oxidative stress, and metastatic potential in murine osteosarcoma cells

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    Osteosarcoma (OS) is the most common primary malignancy of bone. Mortality is determined by the presence of metastatic disease, but little is known regarding the biochemical events that drive metastases. Two murine OS cell lines, K7M2 and K12, are related but differ significantly in their metastatic potentials: K7M2 is highly metastatic whereas K12 displays much less metastatic potential. Using this experimental system, the mammalian target of rapamycin (mTOR) pathway has been implicated in OS metastasis. We also discovered that aldehyde dehydrogenase (ALDH, a stem cell marker) activity is higher in K7M2 cells than K12 cells. Rapamycin treatment reduces the expression and enzymatic activity of ALDH in K7M2 cells. ALDH inhibition renders these cells more susceptible to apoptotic death when exposed to oxidative stress. Furthermore, rapamycin treatment reduces bone morphogenetic protein-2 (BMP2) and vascular endothelial growth factor (VEGF) gene expression and inhibits K7M2 proliferation, migration, and invasion in vitro. Inhibition of ALDH with disulfiram correlated with decreased mTOR expression and activity. In conclusion, we provide evidence for interaction between mTOR activity, ALDH activity, and metastatic potential in murine OS cells. Our work suggests that mTOR and ALDH are therapeutic targets for the treatment and prevention of OS metastasis. © 2013 Xiaodong Mu et al

    Rapamycin inhibits ALDH activity, resistance to oxidative stress, and metastatic potential in murine osteosarcoma cells

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    Osteosarcoma (OS) is the most common primary malignancy of bone. Mortality is determined by the presence of metastatic disease, but little is known regarding the biochemical events that drive metastases. Two murine OS cell lines, K7M2 and K12, are related but differ significantly in their metastatic potentials: K7M2 is highly metastatic whereas K12 displays much less metastatic potential. Using this experimental system, the mammalian target of rapamycin (mTOR) pathway has been implicated in OS metastasis. We also discovered that aldehyde dehydrogenase (ALDH, a stem cell marker) activity is higher in K7M2 cells than K12 cells. Rapamycin treatment reduces the expression and enzymatic activity of ALDH in K7M2 cells. ALDH inhibition renders these cells more susceptible to apoptotic death when exposed to oxidative stress. Furthermore, rapamycin treatment reduces bone morphogenetic protein-2 (BMP2) and vascular endothelial growth factor (VEGF) gene expression and inhibits K7M2 proliferation, migration, and invasion in vitro. Inhibition of ALDH with disulfiram correlated with decreased mTOR expression and activity. In conclusion, we provide evidence for interaction between mTOR activity, ALDH activity, and metastatic potential in murine OS cells. Our work suggests that mTOR and ALDH are therapeutic targets for the treatment and prevention of OS metastasis. © 2013 Xiaodong Mu et al

    SPH Simulations of Direct Impact Accretion in the Ultracompact AM CVn Binaries

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    The ultracompact binary systems V407 Vul (RX J1914.4+2456) and HM Cnc (RX J0806.3+1527) - a two-member subclass of the AM CVn stars - continue to pique interest because they defy unambiguous classification. Three proposed models remain viable at this time, but none of the three is significantly more compelling than the remaining two, and all three can satisfy the observational constraints if parameters in the models are tuned. One of the three proposed models is the direct impact model of Marsh & Steeghs (2002), in which the accretion stream impacts the surface of a rapidly-rotating primary white dwarf directly but at a near-glancing angle. One requirement of this model is that the accretion stream have a high enough density to advect its specific kinetic energy below the photosphere for progressively more-thermalized emission downstream, a constraint that requires an accretion spot size of roughly 1.2x10^5 km^2 or smaller. Having at hand a smoothed particle hydrodynamics code optimized for cataclysmic variable accretion disk simulations, it was relatively straightforward for us to adapt it to calculate the footprint of the accretion stream at the nominal radius of the primary white dwarf, and thus to test this constraint of the direct impact model. We find that the mass flux at the impact spot can be approximated by a bivariate Gaussian with standard deviation \sigma_{\phi} = 164 km in the orbital plane and \sigma_{\theta} = 23 km in the perpendicular direction. The area of the the 2\sigma ellipse into which 86% of the mass flux occurs is roughly 47,400 km^2, or roughly half the size estimated by Marsh & Steeghs (2002). We discuss the necessary parameters of a simple model of the luminosity distribution in the post-impact emission region.Comment: 24 pages, 5 figures, Accepted for publication in Ap

    Rapamycin inhibits ALDH activity, resistance to oxidative stress, and metastatic potential in murine osteosarcoma cells

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    Osteosarcoma (OS) is the most common primary malignancy of bone. Mortality is determined by the presence of metastatic disease, but little is known regarding the biochemical events that drive metastases. Two murine OS cell lines, K7M2 and K12, are related but differ significantly in their metastatic potentials: K7M2 is highly metastatic whereas K12 displays much less metastatic potential. Using this experimental system, the mammalian target of rapamycin (mTOR) pathway has been implicated in OS metastasis. We also discovered that aldehyde dehydrogenase (ALDH, a stem cell marker) activity is higher in K7M2 cells than K12 cells. Rapamycin treatment reduces the expression and enzymatic activity of ALDH in K7M2 cells. ALDH inhibition renders these cells more susceptible to apoptotic death when exposed to oxidative stress. Furthermore, rapamycin treatment reduces bone morphogenetic protein-2 (BMP2) and vascular endothelial growth factor (VEGF) gene expression and inhibits K7M2 proliferation, migration, and invasion in vitro. Inhibition of ALDH with disulfiram correlated with decreased mTOR expression and activity. In conclusion, we provide evidence for interaction between mTOR activity, ALDH activity, and metastatic potential in murine OS cells. Our work suggests that mTOR and ALDH are therapeutic targets for the treatment and prevention of OS metastasis. © 2013 Xiaodong Mu et al

    Evaluation of Adsorption Effects on Measurements of Ammonia, Acetic Acid, and Methanol

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    [1] We examined how adsorption and desorption of gases from inlets and a cell could affect the accuracy of closed-cell FTIR measurements of carbon dioxide (CO2), carbon monoxide (CO), methane (CH4), nitric oxide (NO), nitrogen dioxide (NO2), methanol (CH3OH), acetic acid (CH3COOH), and ammonia (NH3). When standards were delivered to the cell through a stainless steel inlet, temporarily reduced transmission was observed for CH3OH and NH3. However, a halocarbon wax coated inlet (normally used on the system) had excellent transmission (comparable to room temperature Teflon) for both CH3OH and NH3, even at temperatures as low as 5°C. Thus the wax is valuable for coating sampling system components that cannot be fashioned from Teflon. The instrument had a delayed response (∼10–40 s) for NH3 only, which was attributed to passivation of the Pyrex multipass cell. To determine sampling artifacts that could arise from the complex sample matrix presented by smoke, the closed-cell FTIR system was intercompared with an open-path FTIR system (which is immune to sampling artifacts) in well-mixed smoke. A similar cell passivation delay for NH3 was the only artifact found in this test. Overall, the results suggest that ∼10 s is sufficient to detect \u3e80% of an NH3/CO ratio sampled by our fast-flow, closed-cell system. Longer sampling times or consecutive samples return better results. In field campaigns the closed-cell system sampling times were normally 10 to \u3e100 s so NH3 was probably underestimated by 5–15%

    Comparison of Tracking-By-Detection Algorithms for Real-Time Satellite Component Tracking

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    With space becoming more and more crowded, there is a growing demand for increasing satellite lifetimes and performing on-orbit servicing (OOS) at a scale that calls for autonomous missions. Many such missions would require chaser satellites to autonomously execute safe and effective flightpath to dock with a non-cooperative target satellite on orbit. Performing this autonomously requires the chaser to be aware of hazards to route around and safe capture points through time, i.e., by first identifying and tracking key components of the target satellite. State-of-the-art object detection algorithms are effective at detecting such objects on a frame-by-frame basis. However, implementing them on a real-time video feed often results in poor performance at tracking objects over time, making errors which could be easily corrected by rejecting non-physical predictions or by exploiting temporal patterns. On the other hand, dedicated object tracking algorithms can be far too computationally expensive for spaceflight computers. Considering this, the paradigm of tracking-by-detection works by incorporating patterns of prior-frame detections and the corresponding physics in tandem with a base object detector. This paper focuses on comparing the performance of object tracking-by-detection algorithms with a YOLOv8 base object detector: namely, BoTSORT and ByteTrack. These algorithms are hardware-in-the-loop tested for autonomous spacecraft component detection for a simulated tumbling target satellite. This will emulate mission conditions, including motion and lighting, with a focus on operating under spaceflight computational and power limitations, providing an experimental comparison of performance. Results demonstrate lightweight tracking-by-detection can improve the reliability of autonomous vision-based navigation

    Examining the Acute Effects of Virtual Reality on the Star Excursion Balance Test in Chronic Ankle Instability

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    Chronic ankle instability (CAI) patients display mechanical and functional restrictions, along with neurocognitive dysfunction after lateral ankle sprains. Athletes need to divide their attention to effectively multitask during sports activities. Recent studies have utilized virtual reality (VR) to simulate dynamic sporting environments, aiming to enhance cognitive and postural control. However, little is known about the acute effects of VR on dynamic postural control in CAI patients. PURPOSE: To identify the acute effects of VR gear on dynamic postural control in CAI patients. METHODS: This study was a cross-over study. Twenty CAI patients (11males, 9females; age=21±3year; height=1.63±0.28m; mass=74±13.1kg). We used the Foot and Ankle Ability Measures and Ankle Instability Instrument questionnaires for CAI. VR training included 3 trials of single-leg stance; double and single-leg drop landings; and 5 trials of jump landing/cutting. Before and after VR training, participants performed 3 trials each in 3 directions: anterior (ANT), posteromedial (PM), and posterolateral (PL). The average reach distance was normalized by an individual’s leg length from the anterior superior iliac spine to the distal end of the medial malleolus. Matched paired t-tests were used to evaluate the acute effect (posttest-pretest difference) of VR training. The significance level for all analyses was set at a priori of p≤0.05. RESULTS: Acute effects were not observed in both ANT and PM directions (60.2±7.2 vs. 60.9±6.9, p=0.15 and 103.3±10.4 vs. 104.6±11.2, p=0.31). CAI patients showed an acute effect, improving PL reach distance (98.3±11.2 vs. 102.1±13.3, p=0.006) during the star excursion balance test after VR training. CONCLUSION: VR resulted in no difference in ANT direction, which is related to the dorsiflexion range of motion, suggesting that VR training had no improvement in mechanical restriction. After VR training, PL reach distance was increased, suggesting improvement in functional restriction in CAI patients. Therefore, VR training may affect functional restriction, by potentially increasing eversion strength and improving mediolateral static postural control. More data are needed to determine if VR may reduce the risk of recurrent ankle sprains in CAI patients
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