724 research outputs found

    Solar and biomass hybridization through hydrothermal carbonization

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    Hydrothermal carbonization process can transform wet bio-wastes into value-added products. This work aims to hybridize a concentrating solar technology and a biomass reactor for the continuous and sustainable valorization of biomass. The novel technology proposed integrates a linear beam-down solar field with a twin-screw reactor for continuous HTC process. The solar field consists of two reflections that concentrate linearly the sun energy on the ground, where the twin-screw reactor is placed. A mathematical model is proposed to solve both the heat transfer and HTC kinetics for a co-rotating twin-screw reactor. The incoming heat flux from the solar field (8-20 kW/m(2)), the reactor length (L/D = 30-60 where D is the diameter) and the rotating velocity of the screw (25-100 rpm) are the main variables used to process the biomass up to the desired severity factor. The simulation results of different lignocellulosic biomasses (loblolly pine, sugarcane bagasse, corn stover and rice husk) are validated against literature data. The developed model shows good agreement with experimental results shown in the literature. The proposed technology foresees hydrochar yields of 64-78% for severity factors of 4.2 and 5.3, respectively, in agreement to the experimental results of 63-70% shown in literature. (C) 2021 Elsevier Ltd. All rights reserved

    Value of Serum NEUROG1 Methylation for the Detection of Advanced Adenomas and Colorectal Cancer

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    Aberrant DNA methylation detected in liquid biopsies is a promising approach for colorectal cancer (CRC) detection, including premalignant advanced adenomas (AA). We evaluated the diagnostic capability of serum NEUROG1 methylation for the detection of AA and CRC. A CpG island in NEUROG1 promoter was assessed by bisulfite pyrosequencing in a case-control cohort to select optimal CpGs. Selected sites were evaluated through a nested methylation-specific qPCR custom assay in a screening cohort of 504 asymptomatic family-risk individuals. Individuals with no colorectal findings and benign pathologies showed low serum NEUROG1 methylation, similar to non-advanced adenomas. Contrarily, individuals bearing AA or CRC (advanced neoplasia-AN), exhibited increased NEUROG1 methylation. Using >1.3518% as NEUROG1 cut-off (90.60% specificity), 33.33% of AN and 32.08% of AA were identified, detecting 50% CRC cases. Nonetheless, the combination of NEUROG1 with fecal immunochemical test (FIT), together with age and gender through a multivariate logistic regression resulted in an AUC = 0.810 for AN, and 0.796 for AA, detecting all cancer cases and 35-47% AA (specificity 98-95%). The combination of NEUROG1 methylation with FIT, age and gender demonstrated a convenient performance for the detection of CRC and AA, providing a valuable tool for CRC screening programs in asymptomatic individuals

    TP53, ATRX alterations, and low tumor mutation load feature IDH-wildtype giant cell glioblastoma despite exceptional ultra-mutated tumors

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    Background: Giant cell glioblastoma (gcGBM) is a rare morphological variant of IDH-wildtype (IDHwt) GBM that occurs in young adults and have a slightly better prognosis than "classic" IDHwt GBM. Methods: We studied 36 GBMs, 14 with a histopathological diagnosis of gcGBM and 22 with a giant cell component. We analyzed the genetic profile of the most frequently mutated genes in gliomas and assessed the tumor mutation load (TML) by gene-targeted next-generation sequencing. We validated our findings using The Cancer Genome Atlas (TCGA) data. Results: p53 was altered by gene mutation or protein overexpression in all cases, while driver IDH1, IDH2, BRAF, or H3F3A mutations were infrequent or absent. Compared to IDHwt GBMs, gcGBMs had a significant higher frequency of TP53, ATRX, RB1, and NF1 mutations, while lower frequency of EGFR amplification, CDKN2A deletion, and TERT promoter mutation. Almost all tumors had low TML values. The high TML observed in only 2 tumors was consistent with POLE and MSH2 mutations. In the histopathological review of TCGA IDHwt, TP53-mutant tumors identified giant cells in 37% of the cases. Considering our series and that of the TCGA, patients with TP53-mutant gcGBMs had better overall survival than those with TP53wt GBMs (log-rank test, P < .002). Conclusions: gcGBMs have molecular features that contrast to "classic" IDHwt GBMs: unusually frequent ATRX mutations and few EGFR amplifications and CDKN2A deletions, especially in tumors with a high number of giant cells. TML is frequently low, although exceptional high TML suggests a potential for immune checkpoint therapy in some cases, which may be relevant for personalized medicine

    Fluctuations of wave functions about their classical average

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    Quantum-classical correspondence for the average shape of eigenfunctions and the local spectral density of states are well-known facts. In this paper, the fluctuations that quantum mechanical wave functions present around the classical value are discussed. A simple random matrix model leads to a Gaussian distribution of the amplitudes. We compare this prediction with numerical calculations in chaotic models of coupled quartic oscillators. The expectation is broadly confirmed, but deviations due to scars are observed.Comment: 9 pages, 6 figures. Sent to J. Phys.

    Holonomy from wrapped branes

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    Compactifications of M-theory on manifolds with reduced holonomy arise as the local eleven-dimensional description of D6-branes wrapped on supersymmetric cycles in manifolds of lower dimension with a different holonomy group. Whenever the isometry group SU(2) is present, eight-dimensional gauged supergravity is a natural arena for such investigations. In this paper we use this approach and review the eleven dimensional description of D6-branes wrapped on coassociative 4-cycles, on deformed 3-cycles inside Calabi-Yau threefolds and on Kahler 4-cycles.Comment: 1+8 pages, Latex. Proceedings of the Leuven workshop, 2002. v2: Corrected typos in equations (4)-(8

    Oncogenic driver mutations predict outcome in a cohort of head and neck squamous cell carcinoma (HNSCC) patients within a clinical trial

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    234 diagnostic formalin-fixed paraffin-embedded (FFPE) blocks from homogeneously treated patients with locally advanced head and neck squamous cell carcinoma (HNSCC) within a multicentre phase III clinical trial were characterised. The mutational spectrum was examined by next generation sequencing in the 26 most frequent oncogenic drivers in cancer and correlated with treatment response and survival. Human papillomavirus (HPV) status was measured by p16INK4a immunohistochemistry in oropharyngeal tumours. Clinicopathological features and response to treatment were measured and compared with the sequencing results. The results indicated TP53 as the most mutated gene in locally advanced HNSCC. HPV-positive oropharyngeal tumours were less mutated than HPV-negative tumours in TP53 (p < 0.01). Mutational and HPV status influences patient survival, being mutated or HPV-negative tumours associated with poor overall survival (p < 0.05). No association was found between mutations and clinicopathological features. This study confirmed and expanded previously published genomic characterization data in HNSCC. Survival analysis showed that non-mutated HNSCC tumours associated with better prognosis and lack of mutations can be identified as an important biomarker in HNSCC. Frequent alterations in PI3K pathway in HPV-positive HNSCC could define a promising pathway for pharmacological intervention in this group of tumours

    Probabilistic reframing for cost-sensitive regression

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    © ACM, 2014. This is the author's version of the work. It is posted here by permission of ACM for your personal use. Not for redistribution. The definitive version was published in ACM Transactions on Knowledge Discovery from Data (TKDD), VOL. 8, ISS. 4, (October 2014) http://doi.acm.org/10.1145/2641758Common-day applications of predictive models usually involve the full use of the available contextual information. When the operating context changes, one may fine-tune the by-default (incontextual) prediction or may even abstain from predicting a value (a reject). Global reframing solutions, where the same function is applied to adapt the estimated outputs to a new cost context, are possible solutions here. An alternative approach, which has not been studied in a comprehensive way for regression in the knowledge discovery and data mining literature, is the use of a local (e.g., probabilistic) reframing approach, where decisions are made according to the estimated output and a reliability, confidence, or probability estimation. In this article, we advocate for a simple two-parameter (mean and variance) approach, working with a normal conditional probability density. Given the conditional mean produced by any regression technique, we develop lightweight “enrichment” methods that produce good estimates of the conditional variance, which are used by the probabilistic (local) reframing methods. We apply these methods to some very common families of costsensitive problems, such as optimal predictions in (auction) bids, asymmetric loss scenarios, and rejection rules.This work was supported by the MEC/MINECO projects CONSOLIDER-INGENIO CSD2007-00022 and TIN 2010-21062-C02-02, and TIN 2013-45732-C4-1-P and GVA projects PROMETEO/2008/051 and PROMETEO2011/052. Finally, part of this work was motivated by the REFRAME project (http://www.reframe-d2k.org) granted by the European Coordinated Research on Long-term Challenges in Information and Communication Sciences & Technologies ERA-Net (CHIST-ERA) and funded by Ministerio de Economia y Competitividad in Spain (PCIN-2013-037).Hernández Orallo, J. (2014). Probabilistic reframing for cost-sensitive regression. ACM Transactions on Knowledge Discovery from Data. 8(4):1-55. https://doi.org/10.1145/2641758S15584G. Bansal, A. Sinha, and H. Zhao. 2008. 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    Systemic Effects Induced by Hyperoxia in a Preclinical Model of Intra-abdominal Sepsis

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    Supplemental oxygen is a supportive treatment in patients with sepsis to balance tissue oxygen delivery and demand in the tissues. However, hyperoxia may induce some pathological effects. We sought to assess organ damage associated with hyperoxia and its correlation with the production of reactive oxygen species (ROS) in a preclinical model of intra-abdominal sepsis. For this purpose, sepsis was induced in male, Sprague-Dawley rats by cecal ligation and puncture (CLP). We randomly assigned experimental animals to three groups: control (healthy animals), septic (CLP), and sham-septic (surgical intervention without CLP). At 18 h after CLP, septic (n = 39), sham-septic (n = 16), and healthy (n = 24) animals were placed within a sealed Plexiglas cage and randomly distributed into four groups for continuous treatment with 21%, 40%, 60%, or 100% oxygen for 24 h. At the end of the experimental period, we evaluated serum levels of cytokines, organ damage biomarkers, histological examination of brain and lung tissue, and ROS production in each surviving animal. We found that high oxygen concentrations increased IL-6 and biomarkers of organ damage levels in septic animals, although no relevant histopathological lung or brain damage was observed. Healthy rats had an increase in IL-6 and aspartate aminotransferase at high oxygen concentration. IL-6 levels, but not ROS levels, are correlated with markers of organ damage. In our study, the use of high oxygen concentrations in a clinically relevant model of intra-abdominal sepsis was associated with enhanced inflammation and organ damage. These findings were unrelated to ROS release into circulation. Hyperoxia could exacerbate sepsis-induced inflammation, and it could be by itself detrimental. Our study highlights the need of developing safer thresholds for oxygen therapy
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