222 research outputs found

    A crack-tracking technique for localized cohesive-frictional damage

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    This paper extends the use of crack-tracking techniques within the smeared crack approach for the numerical simulation of cohesive–frictional damage on quasi-brittle materials. The mechanical behaviour is described by an isotropic damage model with a Mohr–Coulomb failure surface. The correct crack propagation among the two alternative fracture planes proposed by the Mohr–Coulomb theory is selected with the use of an energy criterion based on the total elastic strain energy. The simulation of three benchmark problems of mixed-mode fracture in concrete demonstrates that the proposed methodology can reproduce the material’s frictional characteristics, showing robustness, as well as mesh-size and mesh-bias independence

    Seismic Vulnerability Assessment Method for Vernacular Architecture Considering Uncertainty

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    Built vernacular heritage embraces buildings that are not designed by specialists, but are part of a process that involves many people over many generations and relies on empirical knowledge. Its value as a key-element for cultural identity is unquestionable. However, precisely due to its empirical and traditional nature, it is often seen as an obsolete and unsafe way of construction, which leads to its progressive abandonment. This lack of proper construction details and poor maintenance increases the seismic vulnerability of the vernacular heritage. There is an evident need for simplified easy-to-use seismic vulnerability assessment methods for vernacular architecture, given the generalized lack of resources that can be normally assigned to its study and preservation. Most of the times, visual inspection will be the only tool available to carry out the assessment. Nevertheless, simplified methods demand a deep understanding of the seismic behavior of vernacular architecture. This is a complex task given the great heterogeneity in the geometrical, structural, construction and material characteristics of vernacular buildings. The present works explores the development of a probabilistic method for the analytical derivation of seismic fragility functions of vernacular buildings considering uncertainty in material parameters and structural characteristics. The procedure followed to investigate the effect of uncertainty and to evaluate the influence of a set of key parameters on the seismic response of vernacular buildings is based on stochastic analysis. In the end, a simplified numerical tool is proposed which can be applied based on visual inspection. The process applied and shown here is considered as an example of application and can be replicated in other contexts. It ultimately intends to extend the applicability and reliability of current seismic vulnerability assessment methods

    Seismic Vulnerability Assessment of Representative Building Typologies from Barcelona‘s Eixample District

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    Unreinforced masonry buildings prevail in many old historical centres and urban areas worldwide. These structures may present inadequate seismic performance because they were often designed without considering any seismic resistance requirements. Therefore, they may be highly vulnerable and susceptible to damage caused by earthquakes, even of low intensity. This work investigates the seismic vulnerability of typical unreinforced masonry buildings situated in the Eixample district of Barcelona, Spain. Most of the buildings of the district were designed only for vertical static loads with slender load-bearing masonry walls and flexible diaphragms. A typical characteristic is the presence of openings with considerable size on the facades. The identification of the main parameters affecting the structural behaviour under lateral loading is necessary to evaluate the seismic vulnerability. As a first step, a building taxonomy for the Eixample district has been prepared in order to classify the different building typologies by taking into account the influence of the structural features in the overall response. This typology classification serves two aims. The first aim is to empirically evaluate the vulnerability of each category. The second one is to provide the basis for creating a numerical model of a representative building and analyse its seismic performance. The main objective of this paper is to assess the seismic behaviour of a typical unreinforced masonry structure by means of nonlinear static analysis. For this purpose, a three-dimensional Finite Element model of a representative building has been prepared. Pushover analyses have been performed in two directions (parallel and perpendicular to the façades) aiming to identify the typical failure mechanisms and the seismic capacity. The performance of the representative building typology, with its typical heterogeneities and irregularities, is compared with that of a reference regular unreinforced masonry structure. Additionally, a parametric analysis is carried out to evaluate the different seismic response by adding more storeys in height. This work is the basis for future analyses devoted to large scale seismic vulnerability assessment of the most representative building typologies of the Eixample district

    Cancer burden in adolescents and young adults in Europe

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    Background Cancer epidemiology is unique in adolescents and young adults (AYAs; aged 15-39 years). The European Society for Medical Oncology/European Society for Paediatric Oncology (ESMO/SIOPE) AYA Working Group aims to describe the burden of cancers in AYAs in Europe and across European Union (EU) countries. Patients and methods We used data available on the Global Cancer Observatory. We retrieved crude and age-standardised (World Standard Population) incidence and mortality rates. We reported about AYA cancer burden in Europe and between 28 EU member states. We described incidence and mortality for all cancers and for the 13 cancers most relevant to the AYA population. Results Incidence and mortality varied widely between countries with the highest mortality observed in Eastern EU countries. Cancers of the female breast, thyroid and male testis were the most common cancers across countries followed by melanoma of skin and cancers of the cervix. Variations in cancer incidence rates across different populations may reflect different distribution of risk factors, variations in the implementation or uptake of screening as well as overdiagnosis. AYA cancer mortality disparities may be due to variation in early-stage diagnoses, different public education and awareness of cancer symptoms, different degrees of access or availability of treatment. Conclusions Our results highlight the future health care needs and requirements for AYA-specialised services to ensure a homogeneous treatment across different countries as well as the urgency for preventive initiatives that can mitigate the increasing burden

    Care of adolescents and young adults with cancer in Asia: results of an ESMO/SIOPE/SIOP Asia survey

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    Background Adolescents and young adults (AYAs) with cancer require dedicated management encompassing both adult and paediatric cancer services. Following a European survey, the European Society for Medical Oncology, the European Society for Paediatric Oncology and the Asian continental branch of International Society of Paediatric Oncology undertook a similar survey to assess AYA cancer care across Asia. Methods A link to the online survey was sent to healthcare professionals (HCPs) in Asia interested in AYA cancer care. Questions covered the demographics and training of HCPs, their understanding of AYA definition, availability and access to specialised AYA services, the support and advice offered during and after treatment, and factors of treatment non-compliance. Results We received 268 responses from 22 Asian countries. There was a striking variation in the definition of AYA (median lower age 15 years, median higher age 29 years). The majority of the respondents (78%) did not have access to specialised cancer services and 73% were not aware of any research initiatives for AYA. Over two-thirds (69%) had the option to refer their patients for psychological and/or nutritional support and most advised their patients on a healthy lifestyle. Even so, 46% did not ask about smokeless tobacco habits and only half referred smokers to a smoking cessation service. Furthermore, 29% did not promote human papillomavirus vaccination for girls and 17% did not promote hepatitis B virus vaccination for high-risk individuals. In terms of funding, 69% reported governmental insurance coverage, although 65% reported that patients self-paid, at least partially. Almost half (47%) reported treatment non-compliance or abandonment as an issue, attributed to financial and family problems (72%), loss of follow-up (74%) and seeking of alternative treatments (77%). Conclusions Lack of access to and suboptimal delivery of AYA-specialised cancer care services across Asia pose major challenges and require specific interventions

    Anticancer activity of a sub-fraction of dichloromethane extract of Strobilanthes crispus on human breast and prostate cancer cells in vitro

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    <p>Abstract</p> <p>Background</p> <p>The leaves of <it>Strobilanthes crispus </it>(<it>S. crispus</it>) which is native to the regions of Madagascar to the Malay Archipelago, are used in folk medicine for their antidiabetic, diuretic, anticancer and blood pressure lowering properties. Crude extracts of this plant have been found to be cytotoxic to human cancer cell lines and protective against chemically-induced hepatocarcinogenesis in rats. In this study, the cytotoxicity of various sub-fractions of dichloromethane extract isolated from the leaves of <it>S. crispus </it>was determined and the anticancer activity of one of the bioactive sub-fractions, SC/D-F9, was further analysed in breast and prostate cancer cell lines.</p> <p>Methods</p> <p>The dichloromethane extract of <it>S. crispus </it>was chromatographed on silica gel by flash column chromatography. The ability of the various sub-fractions obtained to induce cell death of MCF-7, MDA-MB-231, PC-3 and DU-145 cell lines was determined using the LDH assay. The dose-response effect and the EC<sub>50 </sub>values of the active sub-fraction, SC/D-F9, were determined. Apoptosis was detected using Annexin V antibody and propidium iodide staining and analysed by fluorescence microscopy and flow cytometry, while caspase 3/7 activity was detected using FLICA caspase inhibitor and analysed by fluorescence microscopy.</p> <p>Results</p> <p>Selected sub-fractions of the dichloromethane extract induced death of MCF-7, MDA-MB-231, PC-3 and DU-145 cells. The sub-fraction SC/D-F9, consistently killed breast and prostate cancer cell lines with low EC<sub>50 </sub>values but is non-cytotoxic to the normal breast epithelial cell line, MCF-10A. SC/D-F9 displayed relatively higher cytotoxicity compared to tamoxifen, paclitaxel, docetaxel and doxorubicin. Cell death induced by SC/D-F9 occurred via apoptosis with the involvement of caspase 3 and/or 7.</p> <p>Conclusions</p> <p>A dichloromethane sub-fraction of <it>S. crispus </it>displayed potent anticancer activities <it>in vitro </it>that can be further exploited for the development of a potential therapeutic anticancer agent.</p

    Biomarkers characterization of circulating tumour cells in breast cancer patients

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    Introduction: Increasing evidence supports the view that the detection of circulating tumor cells (CTCs) predicts outcomes of nonmetastatic breast cancer patients. CTCs differ genetically from the primary tumor and may contribute to variations in prognosis and response to therapy. As we start to understand more about the biology of CTCs, we can begin to address how best to treat this form of disease. Methods: Ninety-eight nonmetastatic breast cancer patients were included in this study. CTCs were isolated by immunomagnetic techniques using magnetic beads labelled with a multi-CK-specific antibody (CK3-11D5) and CTC detection through immunocytochemical methods. Estrogen receptor, progesterone receptor and epidermal growth factor receptor (EGFR) were evaluated by immunofluorescence experiments and HER2 and TOP2A by fluorescence in situ hybridization. We aimed to characterize this set of biomarkers in CTCs and correlate it with clinical-pathological characteristics. Results: Baseline detection rate was 46.9% ≥ 1 CTC/30 ml threshold. CTC-positive cells were more frequent in HER2-negative tumors (p = 0.046). In patients younger than 50 years old, HER2-amplified and G1-G2 tumors had a higher possibility of being nondetectable CTCs. Heterogeneous expression of hormonal receptors (HRs) in samples from the same patients was found. Discordances between HR expression, HER2 and TOP2A status in CTCs and their primary tumor were found in the sequential blood samples. Less that 35% of patients switched their CTC status after receiving chemotherapy. EGFR-positive CTCs were associated with Luminal tumors (p = 0.03). Conclusions: This is the largest exploratory CTC biomarker analysis in nonmetastatic BC patients. Our study suggests that CTC biomarkers profiles might be useful as a surrogate marker for therapeutic selection and monitoring since heterogeneity of the biomarker distribution in CTCs and the lack of correlation with the primary tumor biomarker status were found. Further exploration of the association between EGFR-positive CTCs and Luminal tumors is warranted

    4β-Hydroxywithanolide E from Physalis peruviana (golden berry) inhibits growth of human lung cancer cells through DNA damage, apoptosis and G2/M arrest

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    <p>Abstract</p> <p>Background</p> <p>The crude extract of the fruit bearing plant, <it>Physalis peruviana </it>(golden berry), demonstrated anti-hepatoma and anti-inflammatory activities. However, the cellular mechanism involved in this process is still unknown.</p> <p>Methods</p> <p>Herein, we isolated the main pure compound, 4β-Hydroxywithanolide (4βHWE) derived from golden berries, and investigated its antiproliferative effect on a human lung cancer cell line (H1299) using survival, cell cycle, and apoptosis analyses. An alkaline comet-nuclear extract (NE) assay was used to evaluate the DNA damage due to the drug.</p> <p>Results</p> <p>It was shown that DNA damage was significantly induced by 1, 5, and 10 μg/mL 4βHWE for 2 h in a dose-dependent manner (<it>p </it>< 0.005). A trypan blue exclusion assay showed that the proliferation of cells was inhibited by 4βHWE in both dose- and time-dependent manners (<it>p </it>< 0.05 and 0.001 for 24 and 48 h, respectively). The half maximal inhibitory concentrations (IC<sub>50</sub>) of 4βHWE in H1299 cells for 24 and 48 h were 0.6 and 0.71 μg/mL, respectively, suggesting it could be a potential therapeutic agent against lung cancer. In a flow cytometric analysis, 4βHWE produced cell cycle perturbation in the form of sub-G<sub>1 </sub>accumulation and slight arrest at the G<sub>2</sub>/M phase with 1 μg/mL for 12 and 24 h, respectively. Using flow cytometric and annexin V/propidium iodide immunofluorescence double-staining techniques, these phenomena were proven to be apoptosis and complete G<sub>2</sub>/M arrest for H1299 cells treated with 5 μg/mL for 24 h.</p> <p>Conclusions</p> <p>In this study, we demonstrated that golden berry-derived 4βHWE is a potential DNA-damaging and chemotherapeutic agent against lung cancer.</p
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