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1.
J Toxicol Environ Health A ; 87(10): 428-435, 2024 May 18.
Artigo em Inglês | MEDLINE | ID: mdl-38551404

RESUMO

Alzheimer's disease (AD) is a neurodegenerative disease associated with long non-coding RNAs and DNA methylation; however, the mechanisms underlying the role of lncRNA small nucleolar RNA host gene 1 (lncRNA SNHG1) and subsequent involvement of DNA methylation in AD development are not known. The aim of this study was to examine the regulatory mechanisms attributed to lncRNA SNHG1 gene utilizing 2 strains of senescence-accelerated mouse prone 8 (SAMP8) model of AD and compared to senescence-accelerated mouse resistant (SAMR) considered a control. Both strains of the mouse were transfected with either blank virus, psLenti-U6-SNHG1(low gene expression) virus, and psLenti-pA-SNHG1(gene overexpression) virus via a single injection into the brains for 2 weeks. At 2 weeks mice were subjected to a Morris water maze to determine any behavioral effects followed by sacrifice to extract hippocampal tissue for Western blotting to measure protein expression of p-tau, DNMT1, DNMT3A, DNMT3B, TET1, and p-Akt. No marked alterations were noted in any parameters following blank virus transfection. In SAMP8 mice, a significant decrease was noted in protein expression of DNMT1, DNMT3A, DNMT3B, and p-Akt associated with rise in p-tau and TET1. Transfection with ps-Lenti-U6-SNHG1 alone in SAMR1 mice resulted in a significant rise in DNMTs and p-Akt and a fall in p-tau and TET1. Transfection of SAMP8 with ps-Lenti-U6-SNHG1 blocked effects on overexpression noted in this mouse strain. However, knockdown of lncRNA SNHG1 yielded the opposite results as found in SAMR1 mice. In conclusion, the knockdown of lncRNA SNHG1 enhanced DNA methylation through the PI3K/Akt signaling pathway, thereby reducing the phosphorylation levels of tau in SAMP8 AD model mice with ameliorating brain damage attributed to p-tau accumulation with consequent neuroprotection.


Assuntos
Doença de Alzheimer , Doenças Neurodegenerativas , RNA Longo não Codificante , Camundongos , Animais , Doença de Alzheimer/genética , RNA Longo não Codificante/genética , RNA Longo não Codificante/metabolismo , Metilação de DNA , Proteínas Proto-Oncogênicas c-akt/metabolismo , Doenças Neurodegenerativas/genética , Fosfatidilinositol 3-Quinases/genética , Fosfatidilinositol 3-Quinases/metabolismo
2.
IEEE Trans Image Process ; 33: 2032-2043, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-38470578

RESUMO

Zero-shot learning (ZSL) recognizes unseen images by sharing semantic knowledge transferred from seen images, encouraging the investigation of associations between semantic and visual information. Prior works have been devoted to the alignment of global visual features with semantic information, i.e., attribute vectors, or further mining the local part regions related to each attribute and then simply concatenating them for category decisions. Although effective, these works ignore intrinsic interactions between local parts and the whole object, which enables a more discriminative and representative knowledge transfer for ZSL. In this paper, we propose a Part-Object Progressive Refinement Network (POPRNet), where discriminative and transferable semantics are progressively refined by the cooperation between parts and the whole object. Specifically, POPRNet incorporates discriminative part semantics and object-centric semantics guided by semantic intensity to improve cross-domain transferability. To achieve part-object learning, a semantic-augment transformer (SaT) is proposed to model the part-object relation at the part-level via an encoder and at the object-level via a decoder, generating a comprehensive semantic representation to boost discriminability and transferability. By introducing the prototype updating module embedded with the prototype selection layers, the discriminative ability of the updated category prototype is enhanced to further improve the recognition performance of ZSL. Extensive experiments are conducted to demonstrate the superiority and competitiveness of our proposed POPRNet method on three public benchmark datasets. The code is available at https://github.com/ManLiuCoder/POPRNet.

3.
J Fish Dis ; 47(4): e13919, 2024 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-38217353

RESUMO

Aeromonas jandaei is a gram-negative bacterium commonly found in aquatic environments and can induce illnesses in amphibians, reptiles and aquatic animals. In this study, a strain of bacteria was isolated from the diseased Chinese soft-shell turtle (Pelodiscus sinensis), then named strain JDP-FX. This isolate was identified as A. jandaei after analysis of morphological, physiological and biochemical characteristics, as well as 16S rRNA and gyrB gene sequences. Virulence genetic testing further detected temperature-sensitive protease (eprCAI), type III secretion system (TTSS) (ascv), nuclease (nuc), cytotonic enterotoxin (alt) and serine proteinase (ser) in JDP-FX. Compared with healthy Chinese soft-shell turtle, the serum levels of total protein (TP), albumin (ALB) and globulin (GLB) were significantly decreased in the diseased Chinese soft-shell turtle, while, the levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST) and alkaline phosphatase (ALP) were significantly increased. Histopathological observations showed that multiple tissues, including intestinal mucosa, liver and kidney, were severely damaged in the diseased Chinese soft-shell turtle. Moreover, the diseased Chinese soft-shell turtle had significant cell degeneration, necrosis, sloughing and interstitial inflammatory cell infiltration. The pathogenicity of JDP-FX was tested via artificial infection. The median lethal dosage (LD50 ) of the strain was 1.05 × 105 colony forming units (CFU/g) per weight of Chinese soft-shell turtle. Drug susceptibility analysis revealed that JDP-FX was susceptible to ceftazidime, minocycline, cefoperazone, ceftriaxone and piperacillin. In addition, JDP-FX was resistant to doxycycline, florfenicol, sulfonamides, gentamicin, ampicillin and neomycin. Therefore, this study may provide guidance for further research into the diagnosis, prevention and treatment of JDP-FX infection.


Assuntos
Aeromonas , Doenças dos Peixes , Tartarugas , Animais , Tartarugas/genética , Tartarugas/metabolismo , RNA Ribossômico 16S/genética , RNA Ribossômico 16S/metabolismo , China
4.
J Fish Dis ; 47(1): e13864, 2024 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-37723838

RESUMO

The Chinese revered a species of aquatic reptile known as Pelodiscus sinensis as both an edible and medicinal species. When artificially breeding, many deaths occurred at the farmed P. sinensis, mainly due to excessive breeding density, water contamination, and turtles biting each other secondary to bacterial infections. In this study, an isolate of gram-negative bacteria WH0623 was isolated from the liver and kidney of diseased P. sinensis to trace the potential pathogen of this disease. Based on biochemical characteristics and 16S rRNA gene sequencing analyses, this isolated strain of WH0623 was identified as Chryseobacterium indologenes. The strain's median lethal dose (LD50 ) was 3.3 × 105 colony-forming units (CFU)/g per fish weight tested using artificial infection. Histopathological analysis revealed pathological changes, including cell swelling, hyperaemia, and necrosis in many tissues. Antibiotic susceptibility tests revealed that the bacteria WH0623 was susceptible to doxycycline, sulphonamides, ceftazidime, norfloxacin, and ciprofloxacin. These antibiotics could treat the disease. In conclusion, the pathogen causing the death of farmed P. sinensis was isolated and identified, and a drug-sensitive test was conducted. Our findings contribute to the future diagnosis and treatment of the disease.


Assuntos
Doenças dos Peixes , Tartarugas , Animais , RNA Ribossômico 16S/genética , Doenças dos Peixes/tratamento farmacológico , Antibacterianos/farmacologia , Antibacterianos/uso terapêutico , Tartarugas/genética
5.
Aesthetic Plast Surg ; 47(5): 1957-1966, 2023 10.
Artigo em Inglês | MEDLINE | ID: mdl-37580561

RESUMO

BACKGROUND: The objective of the present study was to assess the hard and soft tissue differences of skeletal Class III malocclusion patients treated with orthodontic-orthognathic surgery treatment between two decompensation approaches including extraction of maxillary premolars in preoperative orthodontics and clockwise rotation of the maxilla in orthognathic surgery. METHODS: 22 skeletal Class III patients with the crowding of maxillary dental arch less than 3mm were included in this study. These patients were divided into two groups: extraction group and non-extraction group. Lateral cephalograms taken before preoperative orthodontic treatment and after postoperative orthodontic treatment were used to analyze the differences of hard and soft tissues between two groups. Independent t test was used to evaluate the differences of variables between extraction group and non-extraction group. RESULTS: After treatment, there was significant difference of Wits between extraction group and non-extraction group (- 4.34 mm vs - 2.82 mm, respectively, P <0.05). Co-Gn was significantly greater in non-extraction group than in extraction group (77.18 mm vs 71.58 mm, P <0.05). U1-SN and L1-MP in extraction group were significantly closer to the normal values than non-extraction group (P <0.05). Regarding the change of variables before and after orthodontic-orthognathic treatment, NLA (7.25° vs 1.46°, P <0.01) and G-Sn-Pog' (8.06° vs 4.62°, P <0.05) were significantly greater in extraction group than in non-extraction group. CONCLUSION: For patients with skeletal Class III malocclusion, extraction of maxillary premolars in preoperative orthodontic treatment can more effectively eliminate the dental compensation and achieve a more harmonious facial profile compared to clockwise rotation of the maxilla in orthognathic surgery. LEVEL OF EVIDENCE IV: This journal requires that authors assign a level of evidence to each article. For a full description of these Evidence-Based Medicine ratings, please refer to the Table of Contents or the online Instructions to Authors www.springer.com/00266 .


Assuntos
Má Oclusão Classe III de Angle , Procedimentos Cirúrgicos Ortognáticos , Humanos , Mandíbula/cirurgia , Má Oclusão Classe III de Angle/cirurgia , Maxila/cirurgia , Cefalometria
6.
Comput Intell Neurosci ; 2023: 2506274, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-36733786

RESUMO

Object detection is one of the most critical areas in computer vision, and it plays an essential role in a variety of practice scenarios. However, small object detection has always been a key and difficult problem in the field of object detection. Therefore, considering the balance between the effectiveness and efficiency of the small object detection algorithm, this study proposes an improved YOLOX detection algorithm (BGD-YOLOX) to improve the detection effect of small objects. We present the BigGhost module, which combines the Ghost model with a modulated deformable convolution to optimize the YOLOX for greater accuracy. At the same time, it can reduce the inference time by reducing the number of parameters and the amount of computation. The experimental results show that BGD-YOLOX has a higher average accuracy rate in terms of small target detection, with mAP0.5 up to 88.3% and mAP0.95 up to 56.7%, which surpasses the most advanced object detection algorithms such as EfficientDet, CenterNet, and YOLOv4.

7.
Microorganisms ; 11(2)2023 Feb 06.
Artigo em Inglês | MEDLINE | ID: mdl-36838373

RESUMO

Listeria monocytogenes has been shown to exhibit antitumor effects. However, the mechanism remains unclear. Autophagy is a cellular catabolic process that mediates the degradation of unfolded proteins and damaged organelles in the cytosol, which is a double-edged sword in tumorigenesis and treatment outcome. Tumor cells display lower levels of basal autophagic activity than normal cells. This study examined the role and molecular mechanism of autophagy in the antitumor effects induced by LM, as well as the combined antitumor effect of LM and the autophagy inhibitor chloroquine (CQ). We investigated LM-induced autophagy in B16F10 melanoma cells by real-time PCR, immunofluorescence, Western blotting, and transmission electron microscopy and found that autophagic markers were increased following the infection of tumor cells with LM. The autophagy pathway in B16F10 cells was blocked with the pharmacological autophagy inhibitor chloroquine, which led to a significant increase in intracellular bacterial multiplication in tumor cells. The combination of CQ and LM enhanced LM-mediated cancer cell death and apoptosis compared with LM infection alone. Furthermore, the combination of LM and CQ significantly inhibited tumor growth and prolonged the survival time of mice in vivo, which was associated with the increased colonization and accumulation of LM and induced more cell apoptosis in primary tumors. The data indicated that the inhibition of autophagy by CQ enhanced LM-mediated antitumor activity in vitro and in vivo and provided a novel strategy to improving the anticancer efficacy of bacterial treatment.

8.
RSC Adv ; 13(6): 4102-4112, 2023 Jan 24.
Artigo em Inglês | MEDLINE | ID: mdl-36756567

RESUMO

Integrating silicon (Si) and graphitic carbon into micron-sized composites by spray-drying holds great potential in developing advanced anodes for high-energy-density lithium-ion batteries (LIBs). However, common graphite particles as graphitic carbon are always too large in three-dimensional size, resulting in inhomogeneous hybridization with nanosized Si (NSi); in addition, the rate capability of graphite is poor owing to sluggish intercalation kinetics. Herein, we integrated graphite nanosheets (GNs) with NSi to prepare porous NSi-GN-C microspheres by spray-drying and subsequent calcination with the assistance of glucose. Two-dimensional GNs with average thickness of ∼80 nm demonstrate superior lithium storage capacity, high conductivity, and flexibility, which could improve the electronic transfer kinetics and structural stability. Moreover, the porous structure buffers the volume expansion of Si during the lithiation process. The obtained NSi-GN-C microspheres manifest excellent electrochemical performance, including high initial coulombic efficiency of 85.9%, excellent rate capability of 94.4% capacity retention after 50 repeated high-rate tests, and good cyclic performance for 500 cycles at 1.0 A g-1. Kinetic analysis and in situ impedance spectra reveal dominant pseudocapacitive behavior with rapid and stable Li+ insertion/extraction processes. Ex situ morphology characterization demonstrates the ultra-stable integrated structure of the NSi-GN-C. The highly active GN demonstrates great potential to improve the lithium storage properties of Si, which provides new opportunity for constructing high-performance anodes for LIBs.

9.
Polymers (Basel) ; 15(4)2023 Feb 14.
Artigo em Inglês | MEDLINE | ID: mdl-36850224

RESUMO

Magnetodielectric properties of prepared ordered microstructured polydimethylsiloxane-based magnetorheological elastomer with the Fe3O4@rGO (Fe3O4@rGO/PDMS-MRE) were investigated to expand the application of magnetorheological elastomer (MRE) in magnetic sensing fields by improving the magnetodielectric effect. Five types of Fe3O4@rGO electromagnetic biphasic composite particles were synthesized by the solvothermal method, and their characterization and magnetic properties were also tested. Microstructurally ordered Fe3O4@rGO/PDMS-MRE samples with different Fe3O4@rGO concentrations were obtained through the magnetic field orientation technique, an experimental platform for magnetodielectric properties was built, and the relative permittivity of the samples was tested under magnetic flux density from 0 to 500 mT. The results show when the ratio of modified Fe3O4 to GO reaches 10:1, the Fe3O4@rGO composite particles exhibit uniform distribution with a flaky structure and strong magnetic properties and have the best bonding effect of composite particles. The relative permittivity of Fe3O4@rGO/PDMS-MRE increases with the rise of Fe3O4@rGO concentration and applied magnetic flux density. The relative permittivity of Fe3O4@rGO/PDMS-MRE with Fe3O4@rGO concentration of 60 wt% reaches 12.934 under the action of 500 mT magnetic flux density, and the magnetodielectric effect is as high as 92.4%. A reasonable mechanism for improving the magnetodielectric effect of ordered microstructured Fe3O4@rGO/PDMS-MRE is proposed.

10.
Mol Biotechnol ; 65(3): 477-490, 2023 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-36030355

RESUMO

Long non-coding RNAs (lncRNAs) are of great significance in the pathogenesis and progression of papillary thyroid carcinoma (PTC). LncRNA tumorigenicity 7 antisense RNA 1 (ST7-AS1) is a newly identified lncRNA serving as an oncogene or tumor suppressor in different tumors; however, the role of ST7-AS1 in PTC remains completely unknown. In this study, ST7-AS1 was mainly distributed in the cytoplasm of PTC cells and presented reduced expression in THCA tumors and PTC cell lines. Functional experiments revealed that overexpressed ST7-AS1 inhibited the viability and proliferation of PTC cells, whereas accelerated the apoptosis of PTC cells. The expression of miR-181b-5p was upregulated and it bound with ST7-AS1 in PTC cells. Moreover, TRIM3 exhibited downregulated expression level in PTC cells and ST7-AS1 elevated TRIM3 expression via harboring miR-181b-5p. Rescue experiments illuminated that knockdown of TRIM3 reversed ST7-AS1 overexpression-induced promotion on PTC cell proliferation and suppression on PTC cell apoptosis. Overall, overexpression of ST7-AS1 enhances apoptosis and represses proliferation of PTC cells via targeting the miR-181b-5p/TRIM3 axis, which may help broaden the horizon and establish the foundation to develop therapeutic strategies for PTC in the future.


Assuntos
MicroRNAs , RNA Longo não Codificante , Neoplasias da Glândula Tireoide , Humanos , Câncer Papilífero da Tireoide/genética , Câncer Papilífero da Tireoide/metabolismo , Câncer Papilífero da Tireoide/patologia , Neoplasias da Glândula Tireoide/metabolismo , RNA Longo não Codificante/genética , RNA Longo não Codificante/metabolismo , MicroRNAs/genética , MicroRNAs/metabolismo , Linhagem Celular Tumoral , Apoptose/genética , Proliferação de Células/genética , Regulação Neoplásica da Expressão Gênica , Movimento Celular/genética
12.
Microb Pathog ; 174: 105921, 2023 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-36470347

RESUMO

Red sea bream iridovirus (RSIV) belongs to the family Iridoviridae, genus Megalocytivirus, which could widely infect marine fish, causing diseases and huge economic losses. Now it has been reported that RSIV was also detected in diseased mandarin fish. Transmission electron microscopy and immunohistochemistry showed that spleen was the main target organ in mandarin fish infected with RSIV. To investigate the immune response mechanism of mandarin fish to RSIV infection, transcriptomics of RSIV-infected mandarin fish was analyzed. A total of 53,040 unigenes were obtained, and there were 21,576 and 17,904 unigenes had significant hit the Nr and SwissProt databases, respectively. In RSIV-infected and non-infected spleen tissues, there were 309 differentially expressed genes (DEGs), including 100 up-regulated genes and 209 down-regulated genes. Gene Ontology database (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways analysis were performed to reveal the function information and give a better understanding of the signal transduction pathways of DEGs. Further analysis of the cytokine-cytokine receptor interactions pathway exhibited that the expression of cytokines was widely activated after viral infection. In addition, ten DEGs were randomly selected and verified by quantitative real-time PCR, which revealed a similar expression tendency as the high-throughput sequencing data. These findings present valuable information that will benefit for better understanding of RSIV infection in mandarin fish.


Assuntos
Infecções por Vírus de DNA , Doenças dos Peixes , Iridoviridae , Iridovirus , Dourada , Viroses , Animais , Iridovirus/genética , Transcriptoma , Iridoviridae/genética , Infecções por Vírus de DNA/veterinária
13.
Arch Microbiol ; 205(1): 20, 2022 Dec 08.
Artigo em Inglês | MEDLINE | ID: mdl-36482126

RESUMO

Salmonella enterica serovar Typhimurium (S. Typhimurium) is a zoonotic pathogen that causes severe gastroenteritis. The 5'-nucleotidases of pathogens can dephosphorylate adenosine phosphates, boost adenosine levels and suppress the pro-inflammatory immune response. In our previous study, an extracellular nuclease, 5'-nucleotidase, was identified in the extracellular proteins of S. Typhimurium. However, the nuclease activity and the function of the 5'-nucleotidase of S. Typhimurium have not been explored. In the present study, deletion of the 5'-nucleotidase gene is dispensable for S. Typhimurium growth, even under environmental stress. Fluorescence microscopy revealed that the 5'-nucleotidase mutant induced more macrophage extracellular traps (METs) than the wild type did. Furthermore, recombinant 5'-nucleotidase protein (r5Nuc) could degrade λDNA, and the nuclease activity of r5Nuc was optimum at 37 °C and pH 6.0-7.0. The Mg2+ enhanced the nuclease activity of r5Nuc, whereas Zn2+ inhibited it. Meanwhile, deletion of the 5'-nucleotidase gene increased the bactericidal activity of METs, and r5Nuc could degrade METs and inhibit the bactericidal activity of METs. In conclusion, S. Typhimurium growth was independent of 5'-nucleotidase, but the nuclease activity of 5'-nucleotidase assisted S. Typhimurium to evade macrophage-mediated extracellular killing through degrading METs.


Assuntos
Armadilhas Extracelulares , Salmonella typhimurium , Salmonella typhimurium/genética , Macrófagos
14.
BMC Biotechnol ; 22(1): 38, 2022 12 06.
Artigo em Inglês | MEDLINE | ID: mdl-36471312

RESUMO

BACKGROUND: Newcastle disease virus (NDV) strain ZM10, a typical enterotropic avirulent vaccine strain, has been widely used in China for chickens against Newcastle disease. To elucidate its enterotropic mechanism and develop recombiant multivalent vaccines based on it, the reverse genetics system for NDV ZM10 is an indispensable platform. RESULTS: A full-length cDNA clone of NDV ZM10 and three supporting plasmids were constructed using the ligation-independent cloning method. Recombinant NDV rZM10 was successfully rescued after these plasmids were co-transfected into BHK-21 cells. Besides, the recombinant virus rZM10-RFP encoding the red fluorescent protein was generated by inserting the RFP gene into the full-length clone of NDV between the P and M genes. These rescued viruses were genetically and biologically identical to the parental strain and showed similar growth kinetics. CONCLUSION: The recovery system of NDV ZM10 strain was established, and can be used as a foundation for research on the enterotropic mechanism and development of multivalent vaccines against viral diseases of livestock and poultry.


Assuntos
Doença de Newcastle , Vírus da Doença de Newcastle , Animais , Vírus da Doença de Newcastle/genética , DNA Complementar/genética , Galinhas/genética , Vacinas Combinadas
15.
IEEE Trans Image Process ; 31: 3056-3065, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-35385381

RESUMO

Zero-shot recognition has been a hot topic in recent years. Since no direct supervision is available, researchers use semantic information as the bridge instead. However, most zero-shot recognition methods jointly model images on the class level without considering the distinctive character of each image. To solve this problem, in this paper, we propose a novel exemplar-based, semantic guided zero-shot recognition method (EBSG). Both visual and semantic information of each image is used. We train visual sub-model to separate each image from the other images of different classes. We also train semantic sub-model to separate this image from the other images described with different semantics. We concatenate the outputs of visual and semantic sub-models to represent images. Image classification model is then learned by measuring visual similarity and semantic consistency of both source and target images. We conduct zero-shot recognition experiments on four widely used datasets. Experimental results show the effectiveness of the proposed EBSG method.

16.
Front Nutr ; 9: 765499, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-35242793

RESUMO

Koumiss is a traditional fermented dairy product with health and medicinal benefits. It is very popular in the Inner Mongolia Autonomous Region of China. The results of relevant studies have shown that koumiss can regulate the gastrointestinal environment, improve the absorption of nutrients, improve the body's intolerance to lactose, enhance the body's immunity, prevent scurvy and atherosclerosis, and aid in the treatment of tuberculosis. However, there are no systematic reports on the effects of koumiss on immunity. In this study, we aimed to decipher the effects of koumiss on intestinal immune modulation. We used liquid chromatography-tandem mass spectrometry (LC-MS) analysis to determine the composition of Koumiss. Using Compound Discoverer software, we compared the mass spectrometry data with the compound information in the online databases ChemSpider and mzCloud to intelligently identify the main chemical components of koumiss. Additionally, we used Mass Frontier small molecule fragmentation libraryTM to determine the structure of fragment ions. A total of 21 components were identified, which clarified the chemical basis of koumiss. These 21 compounds were then used to perform molecular docking with immune-related targets, such as TNF, IL2, IL10, etc. The results indicated good docking activity between most of the compounds and the targets. Then, an immunosuppressive rat model was used to determine the therapeutic effect of koumiss. The results of this study showed that koumiss could, to a certain extent, correct the atrophy of the thymus and spleen in immunosuppressed model rats. The number of leukocytes, lymphocytes, and the CD4+/CD8+ ratio of peripheral blood lymphocytes was also increased. In addition, it could effectively improve the structure of the small intestinal mucosa, which shows that koumiss has a positive effect on the intestinal immune function of immunosuppressed rats. These findings provide an experimental basis for the development and utilization of koumiss as a therapeutic product.

17.
Environ Sci Pollut Res Int ; 29(25): 38385-38394, 2022 May.
Artigo em Inglês | MEDLINE | ID: mdl-35076836

RESUMO

Mounting evidence indicates that lncRNAs (long noncoding RNAs) are involved in the initiation and development of tumors, including non-small cell lung cancer (NSCLC). However, the involvement of C-terminal binding protein-antisense RNA 2 (CTBP1-AS2) in NSCLC remains to be studied. RT-qPCR was carried out to detect CTBP1-AS2 and miR-623 expression in NSCLC cells and tissues. CCK-8 and flow cytometry were performed to measure cell proliferation and cell cycle progression. Luciferase reporter analysis was performed to study the potential target of CTBP1-AS2. We found that CTBP1-AS2 expression was upregulated in NSCLC cells (SPC-A1, A549, H23, and H1299) compared to 16HBE cells. We demonstrated that the CTBP1-AS2 level was higher in NSCLC specimens than in paired non-tumor specimens. Elevated expression of CTBP1-AS2 increased cell growth and induced cell cycle progression and epithelial-mesenchymal transition (EMT). We also found that ectopic expression of CTBP1-AS2 inhibited miR-623 expression. MMP3 was a direct target of miR-623, and luciferase reporter assays suggested that miR-623 overexpression suppressed the luciferase expression driven by the MMP3 wild-type reporter but not the mutant reporter. Overexpression of miR-623 suppressed MMP3 expression in A549 cells, and overexpression of CTBP1-AS2 increased MMP3 expression in A549 cells. Moreover, the miR-623 level was lower in NSCLC specimens than in paired non-tumor specimens, and CTBP1-AS2 expression was negatively correlated with miR-623 expression in NSCLC samples. Furthermore, overexpression of CTBP1-AS2 enhanced cell growth, cell cycle progression, and EMT progression by modulating MMP3 expression.


Assuntos
Carcinoma Pulmonar de Células não Pequenas , Neoplasias Pulmonares , Metaloproteinase 3 da Matriz , MicroRNAs , RNA Longo não Codificante , Carcinoma Pulmonar de Células não Pequenas/genética , Carcinoma Pulmonar de Células não Pequenas/metabolismo , Carcinoma Pulmonar de Células não Pequenas/patologia , Linhagem Celular Tumoral , Proliferação de Células/genética , Progressão da Doença , Humanos , Neoplasias Pulmonares/genética , Neoplasias Pulmonares/metabolismo , Neoplasias Pulmonares/patologia , Metaloproteinase 3 da Matriz/genética , Metaloproteinase 3 da Matriz/metabolismo , MicroRNAs/genética , MicroRNAs/metabolismo , RNA Longo não Codificante/genética , Transdução de Sinais
18.
IEEE Trans Image Process ; 31: 748-758, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-34928798

RESUMO

Recent techniques have achieved remarkable improvements depended on mining subtle yet distinctive features for fine-grained visual classification (FGVC). While prior works directly combine discriminative features extracted from different parts, we argue that the potential interactions between different parts and their abilities to category predictions should be taken into consideration, which enables significant parts to contribute more to the decision of the sub-category. To this end, we present a Cross-Part Convolutional Neural Network (CP-CNN) in a weakly supervised manner to explore cross-learning among multi-regional features. Specifically, the context transformer is implemented to encourage joint feature learning across different parts under the guidance of a navigator. The part with the highest confidence is regarded as a navigator to deliver distinguishing characteristics to the others with lower confidence while the complementary information is retained. To locate discriminative but subtle parts precisely, a part proposal generator (PPG) is designed with the feature enhancement blocks, through which complex scale variations caused by the viewpoint diversity can be effectively alleviated. Extensive experiments on three benchmark datasets demonstrate that our proposed method consistently outperforms existing state-of-the-art methods.

19.
Medicine (Baltimore) ; 100(51): e28233, 2021 Dec 23.
Artigo em Inglês | MEDLINE | ID: mdl-34941090

RESUMO

ABSTRACT: Reoperative thyroidectomy is challenging for surgeons because of the higher incidence of recurrent laryngeal nerve (RLN) palsy. RLN identification is the gold standard during thyroidectomy; however, it is sometimes difficult to perform thyroid reoperations. In recent years, intraoperative nerve monitoring (IONM) has gained increased acceptance, and the use of IONM can be a valuable adjunct to visual identification. The aim of this study was to evaluate the value of IONM during thyroid reoperation.A total of 109 patients who met our criteria at the Affiliated Hospital of Hangzhou Normal University from January 2010 to June 2020 were retrospectively analyzed and divided into the IONM group and the visualization-alone group (VA group) according to whether neuromonitoring was used during the operation. The patients' characteristics, perioperative data, and intraoperative information including the RLN identification, time of RLNs confirmation, operative time, intraoperative blood loss, and the rate of RLN injury were collected.Sixty-five procedures (94 RLNs at risk) were performed in the IONM group, whereas 44 (65 RLNs at risk) were in the VA group. The rate of RLN identification was 96.8% in the IONM group and 75.4% in the VA group (P < .05). The incidence of RLN injury was 5.3% in the IONM group and 13.8% in the VA group (P > .05). The incidence of surgeon-related RLN injury rate was 0% in the IONM group compared to 7.7% in the VA group (P < .05), but the tumor-related or scar-related RLN injury rate between the 2 groups were not significantly different (4.3% vs 3.1%, 1.1% vs 3.1%, P > .05).IONM in thyroid reoperation was helpful in improving the RLN identification rate and reducing the surgeon-related RLN injury rate, but was ineffective in reducing the tumor-related and scar-related RLN injury rate. In the future, multicenter prospective studies with large sample sizes may be needed to further assess the role of IONM in thyroid reoperations.


Assuntos
Traumatismos do Nervo Laríngeo Recorrente , Reoperação , Glândula Tireoide/cirurgia , Tireoidectomia/efeitos adversos , Paralisia das Pregas Vocais , Adulto , Idoso , Cicatriz , Feminino , Humanos , Período Intraoperatório , Masculino , Pessoa de Meia-Idade , Monitorização Intraoperatória , Estudos Prospectivos , Nervo Laríngeo Recorrente , Traumatismos do Nervo Laríngeo Recorrente/prevenção & controle , Estudos Retrospectivos , Paralisia das Pregas Vocais/epidemiologia , Paralisia das Pregas Vocais/etiologia , Paralisia das Pregas Vocais/prevenção & controle
20.
Oncol Lett ; 22(5): 769, 2021 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-34589148

RESUMO

Dishevelled-2 (DVL2) has been proven to be involved in the tumorigenesis of several human cancers, such as colorectal cancer, lung cancer, prostate cancer, etc. However, its role in pancreatic ductal adenocarcinoma (PDAC) remains unclear. The present study investigated the effects of aberrantly expressed DVL2 on PDAC. A total of 97 pancreatic cancer (PC) samples and 85 adjacent normal samples were obtained from patients who were histopathologically diagnosed with primary PDAC. The present study demonstrated that DVL2 expression was upregulated in PDAC tissues and was positively associated with advanced clinical stage and lymph node metastasis in patients with PDAC. In addition, patients with high expression of DVL2 had a shorter overall survival rate compared with those with low expression. To elucidate the role of DVL2 in PDAC, lentivirus-mediated short hairpin RNA was used to silence DVL2 and its physiological function was analyzed in CFPAC-1 and PANC-1 cells. The results indicated that DVL2 downregulation significantly impaired its oncogenic functions including cell proliferation, migration, invasion and epithelial-mesenchymal transition. Furthermore, DVL2 knockdown inhibits the proliferation and invasion of PC cells in vivo. In addition, co-immunoprecipitation assays revealed that DVL2 interacted with ß-catenin; knockdown of DVL2 reduced the expression level of ß-catenin and inhibited ß-catenin translocation into the nucleus. In conclusion the findings of the present study suggested that DVL2 may be a potential therapeutic target in the treatment of PDAC.

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