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1.
Genomics ; 116(1): 110761, 2024 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-38092323

RESUMEN

AIM: To unravel whether ferroptosis involves with the actions by circPDE3B-mediated facilitation of esophageal squamous cell carcinoma (ESCC) progression. METHODS: Human ESCC tissues and cell lines were prepared for the evaluation of ferroptosis. Cellular iron, ROS, GSH, and MDA levels were measured to assess ferroptosis. Flow cytometry was employed to analyze apoptosis and cell cycle. Subcellular fractionation and fluorescence in situ hybridization (FISH) were conducted to validate the localization of circPDE3B. RNA pull-down, RNA immunoprecipitation (RIP), and luciferase assay were subjected to identify the molecular mechanisms. Nude mouse xenograft model was carried out to evaluate the function of circPDE3B/SLC7A11/CBS in vivo. RESULTS: Increased circPDE3B in human ESCC specimens was positively correlated with ferroptosis-related molecules, SLC7A11 and CBS. Functionally, circPDE3B knockdown triggered ferroptosis, apoptosis, and cell cycle arrest in ESCC cells. Whereas, these effects were obviously blocked by miR-516b-5p inhibitor. Mechanistically, not only circPDE3B sponged miR-516b-5p to upregulate CBS, but also directly bound with HNRNPK to stabilize SLC7A11. In mice, depletion of circPDE3B restrained ESCC growth, while this was abolished by overexpression of CBS or SLC7A11. CONCLUSION: In summary, circPDE3B promotes ESCC progression by suppressing ferroptosis through recruiting HNRNPK/SLC7A11 and miR-516b-5p/CBS axes.


Asunto(s)
Neoplasias Esofágicas , Carcinoma de Células Escamosas de Esófago , Ferroptosis , MicroARNs , Humanos , Animales , Ratones , Carcinoma de Células Escamosas de Esófago/patología , Neoplasias Esofágicas/patología , MicroARNs/genética , MicroARNs/metabolismo , Ferroptosis/genética , Hibridación Fluorescente in Situ , Proliferación Celular/genética , Línea Celular Tumoral , Regulación Neoplásica de la Expresión Génica
2.
Opt Express ; 32(8): 13342-13356, 2024 Apr 08.
Artículo en Inglés | MEDLINE | ID: mdl-38859307

RESUMEN

Phase shifting profilometry is an important technique for reconstructing the three-dimensional (3D) geometry of objects with purely diffuse surfaces. However, it is challenging to measure the transparent objects due to the pattern aliasing caused by light refraction and multiple reflections inside the object. In this work, we analyze the aliasing fringe pattern formation for transparent objects and then, propose to learn the front surface light intensity distribution based on the formation principle by using the diffusion models for generating the non-aliased fringe patterns reflected from the front surface only. With the generated fringe patterns, the 3D shape of the transparent objects can be reconstructed via the conventional structured light. We show the feasibility and performance of the proposed method on the data of purely transparent objects that are not seen in the training stage. Moreover, we found it could be generalized to other cases with local-transparent and translucent objects, showing the potential capability of the diffusion based learnable framework in tackling the problems of transparent object reconstruction.

3.
Artículo en Inglés | MEDLINE | ID: mdl-38923044

RESUMEN

PURPOSE: To conduct a large retrospective study of screening refractive error in young children. METHODS: This retrospective study included children aged from 4 months to 8 years in Daxing District, Beijing, who underwent refractive examinations without cycloplegia. It included a cross-sectional assessment of refractive error screening for all children, and a longitudinal component for a subgroup with data available for two to five visits. RESULTS: A total of 14,987 children were included in the cross-sectional study. In the group <1 year of age, the percentage of children with a spherical equivalent (SE) >+2.00 D or with cylinder <-1.50 D was 15.25% and 33.24%, respectively. These were significantly higher than for the 1- to 4-year-old group (SE 8.1% higher, cylinder 13.2% higher) (χ2 = 53.57, p < 0.001; χ2 = 790.39, p < 0.001). Furthermore, 34.83% of children in the 0-year-old group had amblyopia risk factors (ARFs). In the 4-year-old group, boys had a significantly longer axial length (AL) than girls (differences in the right and left eyes were 0.53 and 0.56 mm, respectively; z = 5.48 p < 0.001, z = 5.80, p < 0.001). AL increased with age, while the AL difference between boys and girls remained stable at 4-8 years of age. The percentage of children aged 5-8 years with myopia in 2020-2021 was significantly higher than that in 2018-2019 (H = 12.44, p = 0.006). In the longitudinal study of 4406 children (up to 12-month follow-up), annual changes in SE were -0.27, -0.06, 0.19 and 0.13 D between 0 and 3 years, and -0.38, -0.58, -0.70 and -0.75 D between 5 and 8 years. CONCLUSIONS: Children's refractive error varied significantly from ages 4 months to 1 year, with a high proportion having ARFs. Children aged 5-8 years showed a trend towards myopia. The prevalence of myopia in the cross-sectional analysis in 2020-2021 was greater than in 2018-2019. Screening refraction changed minimally over a 12-month period for children aged 1-3 years, but became more myopic for children aged 5-8 years.

4.
J Cell Biochem ; 124(11): 1764-1778, 2023 11.
Artículo en Inglés | MEDLINE | ID: mdl-37909649

RESUMEN

Curcumin, a kind of natural compound, has been previously proven to inhibit the autophagy in hepatic stellate cells (HSCs) and induce their apoptosis. However, it is not clear whether the enhanced apoptosis of activated HSCs (aHSCs) caused by curcumin depends on autophagy inhibition. We aim to verify this hypothesis and explore the potential mechanisms in this study. Immortalized human HSC line LX-2 was used as an experimental specimen and pretreated with transforming growth factor ß1(TGF-ß1) for 24 h to activate it before drug application. The levels of autophagy, apoptosis, cell activity, lipid metabolism, and the activity of the PI3K/Akt/mTOR signal pathway were evaluated by multiple methods, such as Western blotting, mcherry-EGFP-LC3B adenoviruses transfection, immunofluorescence, Nile Red staining, flow cytometry among others. Our results showed that rapamycin, an autophagy activator, could partly offset the effects of curcumin on autophagy and apoptosis of LX-2 cells, while 3-Methyladenine (3-MA), an autophagy inhibitor, could enhance these effects. Furthermore, curcumin could promote the activity of the PI3K/Akt/mTOR signal pathway in LX-2 cells, while PI3K inhibitor could partly offset this effect and increase the autophagy level. Overall, we demonstrated that curcumin could inhibit the activity and promote LX-2 cells apoptosis by suppressing autophagy by activating the PI3K/Akt/mTOR signal pathway. In addition, lipid recovery and energy deprivation due to autophagy inhibition may be the exact mechanism by which curcumin attenuates the pro-fibrotic activity of LX-2.


Asunto(s)
Curcumina , Células Estrelladas Hepáticas , Humanos , Células Estrelladas Hepáticas/metabolismo , Curcumina/farmacología , Curcumina/metabolismo , Fosfatidilinositol 3-Quinasas/metabolismo , Proteínas Proto-Oncogénicas c-akt/metabolismo , Apoptosis , Serina-Treonina Quinasas TOR/metabolismo , Autofagia , Cirrosis Hepática/metabolismo
5.
Opt Express ; 31(23): 39007-39019, 2023 Nov 06.
Artículo en Inglés | MEDLINE | ID: mdl-38017990

RESUMEN

Reconstruction of moving target surfaces based on active image sensing techniques, such as phase-shifting profilometry, has attracted intensive research in recent years. The measurement error caused by object motion can be addressed successfully by tracking the object movement. However, it either requires high-cost color imaging equipment or is limited by the assumption of 2D translation movement. Therefore, this paper proposes what we believe to be a new method to reconstruct the kinematic object surfaces with any 2D movement sensed by affordable monochrome camera. An improved RAFT optical flow algorithm is proposed to track the object based on the object fringe pattern image directly. The feature points on the object are retrieved immune to the fringe pattern illumination. Then, the RANSAC algorithm and an iteration selection process are employed to select feature points with high quality optical flow. At last, the motion is described mathematically, and the dynamic object is reconstructed successfully. Experiments are presented to verify the effectiveness of the proposed method.

6.
J Gastroenterol Hepatol ; 38(3): 441-450, 2023 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-36652457

RESUMEN

BACKGROUND AND AIM: Whether vitamin D3 (VD3) supplementation is associated with improved liver fibrosis is controversial. METHODS: Liver fibrosis models were treated with VD3, active VD (1,25-OH2 Vitamin D3), or collaboration with GSK126 (Ezh2 inhibitor), respectively. Hepatic stellate cells (HSCs) were co-cultured with hepatocytes and then stimulated with TGF-ß. Autophagy of hepatocytes was determined after the intervention of 1,25-OH2 Vitamin D3 and GSK126. Also, the active status of HSCs and the mechanism with 1,25-OH2 Vitamin D3 and GSK126 intervention were detected. RESULTS: 1,25-OH2 Vitamin D3, but not VD3, is involved in anti-fibrosis and partially improves liver function, which might be associated with related enzymes and receptors (especially CYP2R1), leading to decreased of its biotransformation. GSK126 plays a synergistic role in anti-fibrosis. The co-culture system showed increased hepatocyte autophagy after HSCs activation. Supplementation with 1,25-OH2 Vitamin D3 or combined GSK126 reduced these effects. Further studies showed that 1,25-OH2 Vitamin D3 promoted H3K27 methylation of DKK1 promoter through VDR/Ezh2 due to the weakening for HSCs inhibitory signal. CONCLUSIONS: VD3 bioactive form 1,25-OH2 Vitamin D3 is responsible for the anti-fibrosis, which might have bidirectional effects on HSCs by regulating histone modification. The inhibitor of Ezh2 plays a synergistic role in this process.


Asunto(s)
Colecalciferol , Proteína Potenciadora del Homólogo Zeste 2 , Inhibidores Enzimáticos , Células Estrelladas Hepáticas , Cirrosis Hepática , Humanos , Colecalciferol/metabolismo , Colecalciferol/farmacología , Proteína Potenciadora del Homólogo Zeste 2/antagonistas & inhibidores , Proteína Potenciadora del Homólogo Zeste 2/metabolismo , Proteína Potenciadora del Homólogo Zeste 2/farmacología , Células Estrelladas Hepáticas/metabolismo , Hepatocitos/metabolismo , Hígado/patología , Cirrosis Hepática/tratamiento farmacológico , Cirrosis Hepática/patología , Factor de Crecimiento Transformador beta/metabolismo , Inhibidores Enzimáticos/metabolismo , Inhibidores Enzimáticos/farmacología , Inhibidores Enzimáticos/uso terapéutico
7.
Small ; 18(29): e2202867, 2022 07.
Artículo en Inglés | MEDLINE | ID: mdl-35754302

RESUMEN

Photothermal materials can convert renewable solar energy into thermal energy and have great potential for solar water evaporation. Copper sulfide (Cu2- x S) is an easily available and inexpensive plasmonic material with a high photothermal conversion efficiency and can be applied to solar evaporation and water purification. Monodispersed Cu7 S4 nanoparticles (NPs) and supercrystalline self-assembled superparticles are obtained via wet chemical synthesis and micelle self-assembly. The photothermal properties of the superstructures are investigated using the finite difference time domain method and laser radiation photothermography. The results show that the electromagnetic field intensity and photothermal efficiency of the self-assembly are significantly higher than those of isolated NPs, which is due to the plasmonic coupling of the NPs. The evaporation efficiency of the superstructure is significantly higher than that of isolated NPs, the metal salt ion and total organic carbon concentrations in the waterbody significantly decrease after evaporation, and the water polluted by high salt and organic dye concentrations is purified. The water quality significantly improves after the lake water from Fuxian Lake in the Yunnan-Guizhou Plateau of China is used for solar evaporation. The color changes from pale yellow to colorless and the ion and total organic carbon contents significantly decrease.


Asunto(s)
Energía Solar , Purificación del Agua , Carbono , China , Luz Solar , Purificación del Agua/métodos
8.
Alzheimer Dis Assoc Disord ; 36(4): 368-373, 2022.
Artículo en Inglés | MEDLINE | ID: mdl-36183420

RESUMEN

OBJECTIVE: This study investigated whether α-synuclein and tau in cerebrospinal fluid (CSF) can be used as biomarkers to diagnose dementia with Lewy bodies (DLB). MATERIALS AND METHODS: We retrieved 3303 studies with "Dementia with Lewy bodies," "α-synuclein," and "tau" as keywords. We formulated screening criteria, and 2 researchers completed the screening, quality evaluation, and data extraction tasks. Finally, 35 studies related to tau, and 14 studies related to α-synuclein were included. Review Manager 5.4 and Stata16 were used for meta-analysis. Subgroup, sensitivity, and meta-regression analyses were performed to identify sources of heterogeneity and strengthen the results. RESULTS: Compared with the control group, DLB patients showed significantly higher CSF levels of tau [weighted mean difference=81.36 (59.82, 102.91); Z =7.40; P <0.00001], and lower CSF levels of α-synuclein [weighted mean difference=-95.25 (-162.02, -28.48); Z =2.80; P =0.005]. Mini-Mental State Examination (MMSE) score, male ratio, and disease duration were not sources of heterogeneity on subgroup and meta-regression analyses. Sensitivity analysis revealed no significant differences. CONCLUSIONS: Higher levels of tau and lower levels of α-synuclein were found in the CSF of patients with DLB compared with the control group. Therefore, CSF tau and α-synuclein levels may be diagnostic biomarkers for DLB.


Asunto(s)
Enfermedad de Alzheimer , Enfermedad por Cuerpos de Lewy , Humanos , Masculino , alfa-Sinucleína/líquido cefalorraquídeo , Enfermedad por Cuerpos de Lewy/diagnóstico , Enfermedad por Cuerpos de Lewy/líquido cefalorraquídeo , Proteínas tau/líquido cefalorraquídeo , Enfermedad de Alzheimer/diagnóstico , Biomarcadores/líquido cefalorraquídeo , Péptidos beta-Amiloides/líquido cefalorraquídeo
9.
Neurol Sci ; 43(5): 3145-3152, 2022 May.
Artículo en Inglés | MEDLINE | ID: mdl-34845561

RESUMEN

OBJECTIVES: While many studies have investigated the associations between fibroblast growth factor 20 (FGF20) rs1721100 (C/G) and rs12720208 (C/T) polymorphisms and susceptibility to Parkinson's disease (PD), their results are controversial. Our present meta-analysis estimated the overall association between FGF20 rs1721100 and rs12720208 polymorphisms and the risk of sporadic PD. METHODS: We performed a comprehensive literature search of the PubMed, Web of Science, Embase, Chinese National Knowledge Infrastructure, and Wanfang Medicine electronic databases, which was updated in April 2021. Based on strict inclusion and exclusion criteria, the analysis included a total of 10 papers involving 14 studies with 5262 cases of PD and 6075 controls. Review Manager 5.4 software was used to assess the available data from each study. The pooled odds ratios (ORs) and 95% confidence intervals (CIs) were calculated to assess the association between the FGF20 rs1721100 and rs12720208 polymorphisms and sporadic PD risk. RESULTS: Our results showed that the FGF20 rs1721100 G allele frequency and genotype distribution did not differ between PD patients and controls. Similarly, the FGF20 rs12720208 T allele frequency and genotype distribution did not differ significantly between the two groups. A subgroup analysis of Asian and Caucasian populations also showed the same results. CONCLUSIONS: The results of this meta-analysis indicated that neither the rs1721100 C/G nor the rs12720208 C/T variants were associated with sporadic PD susceptibility.


Asunto(s)
Enfermedad de Parkinson , Pueblo Asiatico/genética , Factores de Crecimiento de Fibroblastos/genética , Predisposición Genética a la Enfermedad/genética , Humanos , Enfermedad de Parkinson/genética , Polimorfismo de Nucleótido Simple/genética
10.
Neurol Sci ; 43(6): 3541-3550, 2022 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-35332438

RESUMEN

OBJECTIVES: Glucocerebrosidase (GBA) gene may be a risk factor for dementia with Lewy bodies (DLB). However, due to the small number of existing studies and the small sample size of previous investigations, it is necessary to conduct objective and quantitative analyses of the association between GBA variants and DLB. There is no consensus regarding the relationship between GBA and the clinical characteristics of DLB. Therefore, we conducted multiple systematic reviews and meta-analyses with a particular focus on the age of onset, sex, and cognitive impairment. METHODS: PubMed, Cochrane, and EMBASE databases were searched to retrieve related studies. The odds ratios and 95% confidence interval were calculated to determine the association between GBA and DLB and between GBA and the clinical characteristics of DLB. RESULTS: Our meta-analysis confirmed that the GBA variant rate was significantly higher in the DLB group than in the control group, as were the variant rates of L444P, N370S, and E326K, whereas the variant rate of T369M showed no significant difference between the groups. Furthermore, the relevant literature was summarised again for meta-analyses. The GBA variant group had a younger age of onset and lower Montreal Cognitive Assessment score than the GBA non-variant group in DLB patients. GBA variants do not differ between sexes in DLB patients. CONCLUSIONS: GBA variants increased the risk of DLB, especially N370S, E326K, and L444P which are strongly associated with DLB, but T369M was not. Patients harbouring GBA variants have an earlier age of onset, more severe cognitive impairment, and rapid symptom progression; however, sex is irrelevant in DLB.


Asunto(s)
Glucosilceramidasa , Enfermedad por Cuerpos de Lewy , Enfermedad de Parkinson , Glucosilceramidasa/genética , Humanos , Enfermedad por Cuerpos de Lewy/genética , Enfermedad de Parkinson/genética , Factores de Riesgo
11.
Ecotoxicol Environ Saf ; 242: 113853, 2022 Sep 01.
Artículo en Inglés | MEDLINE | ID: mdl-35809396

RESUMEN

Various indices based on metal chemical data are used to evaluate pollution and ecological risk, but the consistency of the assessment results is usually unsatisfactory, and it is unclear if the ecological risk from sediment metals is accurately represented in in situ zoobenthos. Herein, the pollution and ecological risk associated with As, Cd, Cr, Cu, Ni, Pb and Zn in the sediments of two adjacent lakes (Datun (DT) and Changqiao (CQ)) were comprehensively evaluated by integrating metal concentrations, chemical forms and bioaccumulation in Bellamya aeruginosa (B. aeruginosa). The metal concentrations and chemical compositions varied widely in the sediments. Over 50% of the Cd, Pb and Zn in the sediments was present in bioavailable forms, followed by 28% of Cu and less than 25% of As, Cr and Ni. According to the enrichment factor (EF) and concentration enrichment ratio (CER) assessments, Cr and Ni were natural in origin, while the other metals were at minor to extremely high pollution levels, with average EFs of 1.5-77.6 and CERs of 1.1-113.4. The pollution levels for Cd, Cu and Pb from the EF and CER assessments were similar, while those for As and Zn were higher according to CER than EF (p = 0.05), likely due to the baseline underestimation associated with the potential diagenetic remobilization of bioavailable metals. The ecological risk index (Er), sediment quality guidelines (SQGs) and risk assessment code (RAC) showed a high eco-risk for Cd, while no similar risk was found for the other metals. By integrating risk indices with the chemical forms and pollution levels of metals, we deduced high eco-risks for As and Pb and moderate eco-risks for Cu and Zn in DT Lake and moderate eco-risks for As, Pb and Zn in CQ Lake. The other metals in the sediments of the two lakes presented low eco-risks. No significant positive correlations (p = 0.05) between metal accumulation in B. aeruginosa and the indices of pollution and eco-risk were observed except for the case of As, implying that measuring the metal concentrations in B. aeruginosa would not accurately characterize the metal pollution and ecological risk of sediments.


Asunto(s)
Gastrópodos , Metales Pesados , Contaminantes Químicos del Agua , Animales , Bioacumulación , Cadmio , China , Monitoreo del Ambiente/métodos , Sedimentos Geológicos/química , Lagos/química , Plomo , Metales Pesados/análisis , Pseudomonas aeruginosa , Medición de Riesgo , Contaminantes Químicos del Agua/análisis
12.
Sensors (Basel) ; 22(19)2022 Oct 06.
Artículo en Inglés | MEDLINE | ID: mdl-36236682

RESUMEN

The intensity of radio waves decays rapidly with increasing propagation distance, and an edge server's antenna needs more power to form a larger signal coverage area. Therefore, the power of the edge server should be controlled to reduce energy consumption. In addition, edge servers with capacitated resources provide services for only a limited number of users to ensure the quality of service (QoS). We set the signal transmission power for the antenna of each edge server and formed a signal disk, ensuring that all users were covered by the edge server signal and minimizing the total power of the system. This scenario is a typical geometric set covering problem, and even simple cases without capacity limits are NP-hard problems. In this paper, we propose a primal-dual-based algorithm and obtain an m-approximation result. We compare our algorithm with two other algorithms through simulation experiments. The results show that our algorithm obtains a result close to the optimal value in polynomial time.

13.
Gastric Cancer ; 24(1): 85-102, 2021 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-32623586

RESUMEN

BACKGROUND: YAP1 is a core protein of the Hippo signaling pathway and is associated with malignancy and immunosuppression. In the present study, we discovered a novel lncRNA, RP11-323N12.5, with tumor promotion and immunosuppression activities through enhancing transcription of YAP1. METHODS: RP11-323N12.5 was identified using GEPIA. Its expression levels and their relationship with clinical features were investigated using clinical samples. The regulation of YAP1 transcription by RP11-323N12.5 was investigated in both GC and T cells, the tumor and immunosuppression promotion roles of RP11-323N12.5 were explored in vitro and in vivo. RESULTS: RP11-323N12.5 was the most up-regulated lncRNA in human GC, based on data from the TCGA database. Its transcription was significantly positively correlated with YAP1 transcription, YAP1 downstream gene expression which contribute to tumor growth and immunosuppression. RP11-323N12.5 promoted YAP1 transcription by binding to c-MYC in the YAP1 promoter region. Meanwhile, transcription of RP11-323N12.5 was also regulated by YAP1/TAZ/TEADs activation in GC cells. RP11-323N12.5 had tumor- and immnosuppression-promoting effects by enhancing YAP1 downstream genes in GC cells. Excessive RP11-323N12.5 was also observed in tumor-infiltrating leukocytes (TILs), which may be exosome-derived and also be related to enhanced Treg differentiation as a result YAP1 up-regulation. Moreover, RP11-323N12.5 promoted tumor growth and immunosuppression via YAP1 up-regulation in vivo. CONCLUSIONS: RP11-323N12.5 was the most up-regulated lncRNA in human GC and it promoted YAP1 transcription by binding to c-MYC within the YAP1 promoter in both GC and T cells. RP11-323N12.5 is an ideal therapeutic target in human GC due to its tumor-promoting and immunosuppression characteristics.


Asunto(s)
Proteínas Adaptadoras Transductoras de Señales/genética , ARN Largo no Codificante/inmunología , Neoplasias Gástricas/genética , Neoplasias Gástricas/inmunología , Factores de Transcripción/genética , Transcripción Genética/genética , Carcinogénesis/genética , Regulación Neoplásica de la Expresión Génica/genética , Humanos , Tolerancia Inmunológica/genética , Transducción de Señal/genética , Regulación hacia Arriba/genética , Proteínas Señalizadoras YAP
14.
Int J Clin Oncol ; 26(2): 284-295, 2021 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-33216242

RESUMEN

OBJECTIVE: Esophageal schwannoma (ES) are rare and mostly benign neurogenic tumors. The clinical misdiagnosis rate of it is high. In this study, the clinicopathologic features of ES in mainland China were studied to better understand the disease and improve the diagnosis and treatment rate. METHODS: A systematic review was conducted in accordance with PRISMA guidelines. The keywords "esophageal schwannoma", "esophageal neurinoma" and "esophageal neurilemoma" were searched for databases such as Pubmed, EMbase, Wanfang Database and Chinese National Knowledge Infrastructure. The search time frame for database was until July 2019. Combined with our patient, the clinicopathological data and the diagnosis and treatment of ES were summarized. RESULTS: ES occurs in the upper part of the mediastinum and in the thoracic esophagus in most patients in the neck, upper and middle segments. CT and PET/CT examinations can be used for diagnosis, but the differentiation value of both benign and malignant ES is similar. The histopathological findings of forceps biopsy specimens are often difficult to diagnose, and deep tissue biopsies may increase pathological accuracy. EUS-FNA is also recommended for ES diagnosis, but it may also be misdiagnosed. Pathological features include a fusiform arrangement in a palisade-like structure or a tumor cell arranged in a network to form a loose structure. ES characteristic immunohistochemistry results showed that S-100 protein has strong immunological activity. CONCLUSION: The definitive diagnosis requires immunohistochemistry, especially immunological reaction with S-100 protein. The appropriate treatment plan should be selected according to the diameter of the lesion. The overall prognosis of ES is good, but attention should be paid to follow-up.


Asunto(s)
Neoplasias Esofágicas , Neurilemoma , China , Endosonografía , Neoplasias Esofágicas/diagnóstico por imagen , Neoplasias Esofágicas/patología , Humanos , Neurilemoma/diagnóstico por imagen , Neurilemoma/patología , Tomografía Computarizada por Tomografía de Emisión de Positrones
15.
BMC Nurs ; 20(1): 38, 2021 Mar 06.
Artículo en Inglés | MEDLINE | ID: mdl-33676508

RESUMEN

BACKGROUND: Collaboration between physicians and nurses is critical. However, a limited number of studies have provided insights into the status of physician-nurse collaboration in truth disclosure. METHODS: A cross-sectional survey was conducted using an electronic questionnaire among Chinese nurses who attended a provincial conference. The Nurse-Physician Collaboration Scale was administered to nurses to assess the collaboration in truth disclosure from their perspective. A multiple-choice question was asked to assess the perceived difficulties in truth disclosure. Descriptive statistics, univariate, and multiple stepwise regression analyses were performed to evaluate physician-nurse collaboration in truth disclosure. RESULTS: A total of 287 nurses completed the survey, and 279 of them reported that they had carried out truth disclosures among patients. The average score for physician-nurse collaboration in truth disclosure was 3.98 ± 0.72. The majority of nurses (73.1-81%) responded positively to different dimensions of collaboration in truth disclosure. The results of multiple stepwise regression analysis showed that seniority (B = - 0.111, 95% confidence interval [CI] = - 0.167-- 0.055, p < 0.001) and frequency of truth disclosure (B = 0.162, 95%CI = 0.076-0.249, p < 0.001) were the only two factors associated with collaboration in truth disclosure between physicians and nurses. The most common barrier perceived by nurses was fear of patients' negative emotions or their suicide attempts after truth telling. CONCLUSIONS: Most nurses responded positively to physician-nurse collaboration in truth disclosure. Various difficulties existed in the practice of truth-telling collaboration. Further studies are required to test the potential interventions to promote cooperation between nurses and physicians in truth disclosure.

16.
Opt Express ; 28(19): 28600-28611, 2020 Sep 14.
Artículo en Inglés | MEDLINE | ID: mdl-32988127

RESUMEN

Many methods have been proposed to reconstruct the moving object based on phase shifting profilometry. Quality reconstruction results can be achieved when a single moving object or multiple objects with same movement are measured. However, errors will be introduced when multiple objects with individual movements are reconstructed. This paper proposes an automated method to track and reconstruct the multiple objects with individual movement. First, the objects are identified automatically and their bounding boxes are obtained. Second, with the identified objects' images before movement, the objects are tracked by the KCF algorithm in the successive fringe pattern after movement. Third, the SIFT method is applied on the tracked object images and the objects' movement is described individually by the rotation matrix and translation vector. Finally, the multiple objects are reconstructed based on the different movement information. Experiments are presented to verify the effectiveness.

17.
Epidemiol Infect ; 148: e104, 2020 05 08.
Artículo en Inglés | MEDLINE | ID: mdl-32381124

RESUMEN

Outbreaks of norovirus-associated gastroenteritis have been reported in schools in recent decades in China. For early warning and response to infectious disease outbreaks, the Shanghai Infectious Diseases Bud Event Surveillance System (IDBESS) was established in 2016. Bud event is a term used for the early sign of a potential infectious disease outbreak in public settings when the first few cases appear. This study aimed to describe the epidemiological characteristics of Norovirus-associated gastroenteritis bud events from June 2016 to December 2017 and to understand factors influencing the severity of events. Data were extracted from the IDBESS, supplemented by field investigations and school absence surveillance. In total, 189 bud events of Norovirus-associated gastroenteritis were reported in schools and kindergartens, affecting 3827 individuals and 52.38% happened in primary schools. The attack rate of Norovirus-associated gastroenteritis was 3.82% on average in students in the affected schools. In each event, case numbers varied between 5 and 148, with a median of 16. The duration of bud events lasted for 2 days on average. School absence happened in 47.93% (1797/3749) of affected students and the average duration of absence was 3.07 days. It was found that a longer delay before reporting was associated with a longer-lasting duration of bud event (OR = 2.25, 95% CI: 1.65, 3.07). In conclusion, ascribed to the sensitive threshold for alerting and the timely field investigation, the surveillance of bud events of Norovirus-associated gastroenteritis is effective in the control of Norovirus infection among preschool children and students in Shanghai.


Asunto(s)
Infecciones por Caliciviridae/prevención & control , Gastroenteritis/prevención & control , Norovirus , Vigilancia de la Población , Instituciones Académicas , Adolescente , Infecciones por Caliciviridae/epidemiología , Niño , Preescolar , China/epidemiología , Brotes de Enfermedades , Femenino , Gastroenteritis/epidemiología , Genotipo , Humanos , Masculino , Norovirus/genética
18.
Cancer Sci ; 110(8): 2507-2519, 2019 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-31215741

RESUMEN

Abnormal tumor microenvironment and the epithelial-mesenchymal transition (EMT) are important features of tumor metastasis. However, it remains unknown how signals can form complicated networks to regulate the sustainability of the EMT process. The aim of our study is to explore the possible interaction between tumor-associated macrophages and tumor cells in the EMT process mediated by microRNA (miR)-362-3p. In this study, we found that by releasing TGF-ß, M2 macrophages mediate binding of Smad2/3 to miR-362-3p promoter, leading to overexpression of miR-362-3p. MicroRNA-362-3p maintains EMT by regulating CD82, one of the most important members of the family of tetraspanins. Our finding suggests that miR-362-3p can serve as a core factor mediating cross-talk between the TGF-ß pathway in tumor-associated macrophages and tetraspanins in tumor cells, and thus facilitates the EMT process.


Asunto(s)
Carcinoma Hepatocelular/metabolismo , Carcinoma Hepatocelular/patología , Transición Epitelial-Mesenquimal/fisiología , Proteína Kangai-1/metabolismo , Neoplasias Hepáticas/metabolismo , Macrófagos/metabolismo , MicroARNs/metabolismo , Factor de Crecimiento Transformador beta/metabolismo , Animales , Línea Celular Tumoral , Regulación Neoplásica de la Expresión Génica/fisiología , Células Hep G2 , Humanos , Neoplasias Hepáticas/patología , Macrófagos/patología , Ratones , Ratones Desnudos , Transducción de Señal/fisiología , Proteína Smad2/metabolismo , Proteína smad3/metabolismo , Tetraspaninas/metabolismo
19.
J Gene Med ; 21(2-3): e3071, 2019 02.
Artículo en Inglés | MEDLINE | ID: mdl-30657227

RESUMEN

INTRODUCTION: The Maonan population is a relatively isolated minority in China. Little is known about endothelial lipase gene (LIPG) single nucleotide polymorphisms (SNPs) and serum lipid levels in the Chinese populations. The present study aimed to detect the association of several LIPG SNPs and environmental factors with serum lipid levels in the Chinese Maonan and Han populations. METHODS: In total, 773 subjects of Maonan ethnicity and 710 participants of Han ethnicity were randomly selected from our previous stratified randomized samples. Genotypes of the LIPG rs2156552, rs4939883 and rs7241918 SNPs were determined by polymerase chain reaction-restriction fragment length polymorphism, and then confirmed by direct sequencing. RESULTS: The allelic (rs2156552, rs4939883 and rs7241918) and genotypic (rs2156552 and rs4939883) frequencies were different between the two ethnic groups (p < 0.05-0.01). The minor allele carriers had lower apolipoprotein (Apo)A1/ApoB ratio (rs2156552 and rs7241918), high-density lipoprotein cholesterol (HDL-C) and apolipoprotein (Apo)A1 (rs2156552) levels and higher ApoB levels (rs4939883) in the Han population, and lower HDL-C (rs2156552, rs4939883 and rs7241918) levels in the Maonan minority than the minor allele non-carriers (p < 0.0167 after Bonferroni correction). Subgroup analyses according to sex showed that the minor allele carriers had a lower ApoA1/ApoB ratio (rs2156552 and rs7241918) and higher ApoB levels (rs7241918) in Han males, and lower ApoA1 and HDL-C levels in Maonan females than the minor allele non-carriers (p < 0.0167-0.001). CONCLUSIONS: The present study demonstrates the association between the LIPG polymorphsims and serum lipid levels in the two ethnic groups. These associations might have an ethnic- and or/sex-specificity.


Asunto(s)
Etnicidad/genética , Lipasa/genética , Lípidos/sangre , Polimorfismo de Nucleótido Simple , Adulto , Anciano , Alelos , Apolipoproteína A-I/sangre , Apolipoproteínas B/sangre , Pueblo Asiatico/etnología , Pueblo Asiatico/genética , China , HDL-Colesterol/sangre , Femenino , Frecuencia de los Genes , Genotipo , Humanos , Masculino , Persona de Mediana Edad
20.
Lipids Health Dis ; 18(1): 10, 2019 Jan 08.
Artículo en Inglés | MEDLINE | ID: mdl-30621702

RESUMEN

BACKGROUND: Maonan nationality is a relatively conservative and isolated minority in the Southwest of China. Little is known about the association of endothelial lipase gene (LIPG) single nucleotide polymorphisms (SNPs) and serum lipid levels in the Chinese populations. METHODS: A total of 1280 subjects of Maonan nationality and 1218 participants of Han nationality were randomly selected from our previous stratified randomized samples. Genotypes of the four LIPG SNPs were determined by polymerase chain reaction-restriction fragment length polymorphism, and then confirmed by direct sequencing. RESULTS: Several SNPs were associated with high-density lipoprotein cholesterol (rs3813082, rs2000813 and rs2097055) in the both ethnic groups; total cholesterol and apolipoprotein (Apo) A1 (rs2000813) in Han nationality; and low-density lipoprotein cholesterol, ApoB, triglyceride (rs2097055) and ApoA1 (rs3819166) in Maonan minority (P < 0.0125 for all after Bonferroni correction). The commonest haplotype was rs3813082T-rs2000813C-rs2097055T-rs3819166A (Han, 44.2% and Maonan, 48.7%). The frequencies of the T-C-T-A, T-C-T-G, T-T-C-G and G-T-C-G haplotypes were different between the Maonan and Han populations (P < 0.05-0.001). The associations between haplotypes and dyslipidemia were also different in the Han and/or Maonan populations (P < 0.05-0.001). CONCLUSIONS: The differences in serum lipid profiles between the two ethnic groups might partly be attributed to these LIPG SNPs, their haplotypes and gene-environmental interactions. TRIAL REGISTRATION: Retrospectively registered.


Asunto(s)
Dislipidemias/etnología , Dislipidemias/genética , Interacción Gen-Ambiente , Lipasa/genética , Polimorfismo de Nucleótido Simple , Adulto , Anciano , Anciano de 80 o más Años , Apolipoproteína A-I/sangre , Apolipoproteína A-I/genética , Apolipoproteína B-100/sangre , Apolipoproteína B-100/genética , China/epidemiología , HDL-Colesterol/sangre , LDL-Colesterol/sangre , Dislipidemias/sangre , Dislipidemias/fisiopatología , Etnicidad , Expresión Génica , Estudios de Asociación Genética , Haplotipos , Humanos , Lipasa/sangre , Masculino , Persona de Mediana Edad , Triglicéridos/sangre
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