12 results on '"Li, Dong‐Ya"'
Search Results
2. Effectiveness of empathy clinical education for children's nursing students: A quasi-experimental study
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Ding, Xiang, Wang, Li, Sun, Jing, Li, Dong-ya, Zheng, Bing-ya, He, Shi-wen, Zhu, Li-hui, and Latour, Jos M.
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- 2020
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3. Exploring NK‐Cell molecules that impact the immune response and microenvironment in head and neck squamous cell carcinoma.
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Shao, Peng, Hu, Wei‐Wei, Shi, Xin‐lian, Shu, Ming‐yang, Li, Dong‐Ya, Zhou, Tingting, and Zhao, Qi‐Tao
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SQUAMOUS cell carcinoma ,IMMUNE response ,KILLER cells ,KI-67 antigen ,NECK ,DATABASES - Abstract
NK cells play a role in various cancers, but their role in head and neck squamous cell carcinoma (HNSCC) still needs to be explored. All public data are obtained from the Cancer Genome Atlas Program (TCGA) database. All analysis was performed using specific packages in R software. In our study, we quantified the immune microenvironment of HNSCC through multiple algorithms. Next, we identified NK cell‐associated genes by quantifying NK cells, including SSNA1, TRIR, PAXX, DPP7, WDR34, EZR, PHLDA1 and ELOVL1. Then, we explored the single‐cell expression pattern of these genes in the HNSCC microenvironment. Univariate Cox regression analysis indicated that the EZR, PHLDA1 and ELOVL1 were related to the prognosis of HNSCC patients. Following this, we selected EZR for further analysis. Our results showed that the patients with high EZR expression might have a poor prognosis and worse clinical features. Biological enrichment analysis showed that EZR is associated with many oncogenic pathways and a higher tumour stemness index. Meanwhile, we found that EZR can remodel the immune microenvironment of HNSCC. Moreover, we noticed that EZR could affect the immunotherapy and specific drug sensitivity, making it an underlying clinical target. In summary, our results can improve the understanding of NK cell in HNSCC. Meanwhile, we identified EZR as the underlying clinical target of HNSCC. [ABSTRACT FROM AUTHOR]
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- 2024
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4. Downregulation of miR-221-3p contributes to IL-1β-induced cartilage degradation by directly targeting the SDF1/CXCR4 signaling pathway
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Zheng, Xin, Zhao, Feng-chao, Pang, Yong, Li, Dong-ya, Yao, Sheng-cheng, Sun, Shao-song, and Guo, Kai-jin
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- 2017
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5. MicroRNA-21-5p as a novel therapeutic target for osteoarthritis.
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Wang, Xiao-bo, Zhao, Feng-chao, Yi, Lin-hong, Tang, Jin-long, Zhu, Zheng-ya, Pang, Yong, Chen, Ye-shuai, Li, Dong-ya, Guo, Kai-jin, and Zheng, Xin
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OSTEOARTHRITIS diagnosis ,PREVENTION of disease progression ,CELL proliferation ,ANIMAL experimentation ,APOPTOSIS ,CARTILAGE ,CARTILAGE cells ,CHEMICAL inhibitors ,EXTRACELLULAR space ,GENE expression ,GROWTH factors ,INTRA-articular injections ,MENISCUS injuries ,MICE ,OLIGONUCLEOTIDES ,OSTEOARTHRITIS ,WESTERN immunoblotting ,TREATMENT effectiveness ,GENE expression profiling ,MICRORNA ,THERAPEUTICS ,DISEASE risk factors - Abstract
Objective Growing evidence indicates that microRNAs (miRNA) play a critical role in the pathogenesis of OA, and overexpressing or silencing miRNA expression in OA models can contribute to the development of miRNA-based therapeutics. The objective of this study was to determine whether intra-articular injection of miRNA can inhibit OA progression. Methods The miRNA expression profile was determined in OA cartilage tissues and controls. Functional analysis of the miRNAs on extracellular matrix degradation was performed after miRNA mimic or inhibitor transfection. Luciferase reporter assays and western blotting were employed to determine miRNA targets. To investigate the functional mechanism of miR-21-5p in OA development, miR-21-5p
fl/fl Col2a1-CreER and wild-type mice were subject to surgical destabilization of the medial meniscus. Therapeutically, wild-type mice undergoing surgical destabilization of the medial meniscus were treated with intra-articular injection of agomir- and antagomir-21-5p. Results We found that expression of miR-21-5p was significantly up-regulated in OA cartilage tissues. The articular cartilage degradation of miR-21-5p conditional knockout mice was significantly alleviated compared with that of wild-type mice in spontaneous and destabilization of the medial meniscus models. Through gain-of-function and loss-of-function studies, miR-21-5p was shown to significantly affect matrix synthesis genes expression, and chondrocyte proliferation and apoptosis. Further, fibroblast growth factor 18 (FGF18) was identified as a target of miR-21-5p. Intra-articular injection of antagomir-21-5p significantly attenuated the severity of experimental OA. Clinically, FGF18 expression level was correlated with miR-21-5p expression and a modified Mankin scale. Conclusion Our findings reveal a miRNA functional pathway important for OA development, highlighting miRNA-21-5p silencing as an attractive therapeutic regimen in future clinical trials involving patients with OA. [ABSTRACT FROM AUTHOR]- Published
- 2019
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6. LINC00641 regulates autophagy and intervertebral disc degeneration by acting as a competitive endogenous RNA of miR‐153‐3p under nutrition deprivation stress.
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Wang, Xiao‐Bo, Wang, Hua, Long, Hou‐Qing, Li, Dong‐Ya, and Zheng, Xin
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AUTOPHAGY ,INTERVERTEBRAL disk ,NON-coding RNA ,DEPRIVATION (Psychology) ,LUCIFERASES ,NUCLEUS pulposus - Abstract
Emerging evidence supports the involvement of autophagy in the pathogenesis of intervertebral disc degeneration (IDD). MicroRNAs (miRNAs) and long noncoding RNAs (lncRNAs) play fundamental roles in various cellular processes, including autophagy. However, it remains largely unknown as to how autophagy is regulated by miRNAs and lncRNAs in IDD. Biological functions of miR‐153‐3p and long intergenic nonprotein coding RNA 641 (LINC00641) were investigated. Luciferase reporter assays was done to validate miR‐153‐3p targets. To induce nutritional stress, nucleus pulposus (NP) cells were cultured in the normal nutritional condition and the low nutritional condition. Quantitative reverse‐transcription polymerase chain reaction (RT‐qPCR) was used to analyze miR‐153‐3p and LINC00641 in response to nutrient deprivation. Autophagic activity was assessed by transmission electron microscopy, western blot analysis and green fluorescent protein‐light chain 3 puncta. Pull‐down assay and RNA fluorescent in situ hybridization were performed to validate LINC00641 target and the location. MiR‐153‐3p is downregulated in NP tissues from IDD patients. Further, LINC00641 can affect collagen II and matrix metalloproteinase‐3 expressions. Upregulation of LINC00641 and downregulation of miR‐153‐3p are detected in NP cells under nutritional stress. LINC00641 can regulate autophagic cell death by targeting miR‐153‐3p and autophagy‐related gene 5 (ATG5). MiR‐153‐3p inhibits autophagy and IDD by targeting ATG5. More important, LINC00641 targets miR‐153‐3p, and thus affects ATG5 expression, autophagic cell death and IDD. These findings uncover a novel regulatory pathway that is composed of LINC00641, miR‐153‐3p, and ATG5 in IDD. This mechanism may stimulate to a more understanding of IDD pathogenesis and provide new sights for the treatment of this disorder. We demonstrated that long intergenic nonprotein coding RNA 641 (LINC00641) acts as endogenous sponge RNA and inhibits miR‐153‐3p expression and its biological function. Therefore, modulation of LINC00641 may represent a novel treatment paradigm in human IDD. These findings shed new light on the importance of the orchestrated interactions between lncRNAs, miRNAs, and autophagy in maintaining cellular homeostasis and suggest that a disturbance in these networks might lead to diseases. [ABSTRACT FROM AUTHOR]
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- 2019
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7. Effect of Chemical Thromboprophylaxis on the Rate of Venous Thromboembolism After Treatment of Foot and Ankle Fractures.
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Zheng, Xin, Li, Dong-Ya, Wangyang, Yufan, Zhang, Xing-Chen, Guo, Kai-Jin, Zhao, Feng-Chao, Pang, Yong, and Chen, Yi-Xin
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Background: Venous thromboembolism (VTE) is a well-documented complication in patients with lower limb fractures, but management guidelines for its prevention in isolated foot and ankle fracture patients are conflicting. The aim of this study was to conduct a multicenter, prospective cohort study to define the prevalence of VTE in patients with isolated foot and ankle fractures and determine whether routine prophylaxis is necessary in these patients. Methods: In a double-blind, placebo-controlled study, consecutive patients in 3 hospitals who met our criteria were enrolled. After randomization, patients received either thromboprophylaxis with low-molecular-weight heparin units (LMWH group) or placebo (placebo group) for a period of 2 weeks. All patients underwent routine ultrasonography 1 day preoperatively, 1 week postoperatively, and 1 month postoperatively. Demographic parameters were then collected and compared. Results: Of the 814 patients who met our criteria, 19 patients (2.3%, 95% confidence interval [CI], 0%-31.9%) were found to have objectively confirmed VTE, but none of the patients were symptomatic. Of the 411 patients in the LMWH group, 2 developed VTEs preoperatively and 4 postoperatively; of the 403 patients in the placebo group, 5 developed VTEs preoperatively and 8 postoperatively. The overall incidence of asymptomatic postoperative deep vein thrombosis (DVT) was 0.98% (95% CI 0%-20.3%) in the LMWH group and 2.01% (95% CI 0%-29.5%) in the placebo group without significant difference. Advanced age (odds ratio [OR] 1.050, 95% CI 1.014-1.088, P = .007) and high body mass index (OR 1.201, 95% CI 1.034-1.395, P = .016) were identified as risk factors in predicting occurrence of DVT. No fatal pulmonary emboli or major bleeding complication occurred in either group. Conclusion: Routine anticoagulant prophylaxis was not found to be necessary for patients with foot and ankle fractures, although further investigation with a properly powered study design is required to definitively determine which foot and ankle patients are best served by anticoagulation and which ones are not. Level of Evidence: Level II, prospective comparative study. [ABSTRACT FROM AUTHOR]
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- 2016
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8. Anatomical study of simple landmarks for guiding the quick access to humeral circumflex arteries.
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Chen, Yi-Xin, Zhu, Yi, Wu, Fu-Hua, Zheng, Xin, Wangyang, Yu-Fan, Yuan, Han, Xie, Xiao-Xiao, Li, Dong-Ya, Wang, Chang-Jun, and Shi, Hong-Fei
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Background: The posterior and anterior circumflex humeral artery (PCHA and ACHA) are crucial for the blood supply of humeral head. We aimed to identify simple landmarks for guiding the quick access to PCHA and ACHA, which might help to protect the arteries during the surgical management of proximal humeral fractures.Methods: Twenty fresh cadavers were dissected to measure the distances from the origins of PCHA and ACHA to the landmarks (the acromion, the coracoid, the infraglenoid tubercle, the midclavicular line) using Vernier calipers.Results: The mean distances from the origin of PCHA to the infraglenoid tubercle, the coracoid, the acromion and the midclavicular line were 27.7 mm, 50.2 mm, 68.4 mm and 75.8 mm. The mean distances from the origin of ACHA to the above landmarks were 26.9 mm, 49.2 mm, 67.0 mm and 74.9 mm.Conclusion: Our study provided a practical method for the intraoperative identification as well as quick access of PCHA and ACHA based on a series of anatomical measurements. [ABSTRACT FROM AUTHOR]- Published
- 2014
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9. Will the untreated ulnar styloid fracture influence the outcome of unstable distal radial fracture treated with external fixation when the distal radioulnar joint is stable.
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Chen, Yi-Xin, Zheng, Xin, Shi, Hong-Fei, Wangyang, Yu-Fan, Yuan, Han, Xie, Xiao-Xiao, Li, Dong-Ya, Wang, Chang-Jun, and Qiu, Xu-Sheng
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Background: The ulnar styloid is an important supportive structure for the triangular fibrocartilage complex. However, it remains inconclusive whether or not a fractured ulnar styloid should be fixed in an unstable distal radius fracture (DRF) with a stable distal radioulnar joint (DRUJ). The purpose of this study is to evaluate the effect of an untreated ulnar styloid fracture on the outcome of unstable DRF treated with transarticular external fixation when the DRUJ is stable.Methods: 106 patients with an unstable DRF and a stable DRUJ were included in this study following external fixation. The patients were divided into the non-fracture, the tip-fracture and the base-fracture groups according to the location of the ulnar styloid fracture at the time of injury. Postoperative evaluation included the range of wrist motion, the radiological index, the grip strength, the PRWE-HK scores, the wrist pain scores, and the instability of DRUJ at the external fixator removal time, three months postoperatively and the final follow-up visit.Results: The patients were followed for 12 to 24 months (15 months in average). Sixty-two of 106 patients (58%) had ulnar styloid fracture and 16 patients (26%) showed radiographic evidence of union of ulnar styloid fractures at the final follow-up visit. No significant difference in the radiological findings, the range of wrist motion, the grip strength, the PRWE-HK scores, and the wrist pain scores among three patient groups was detected at the external fixator removal time, three months postoperatively, or the final follow-up visit. Six of the 106 patients (5.7%) complained of persistent ulnar-side wrist pain during daily activities. One patient (0.9%) showed a positive sign in a stress-test, three patients (2.8%) showed a positive sign in a provocative-test, and five patients (4.7%) showed a positive sign in a press-test. There was no significant difference in the percentages of patients who complained of persistent ulnar-side wrist pain or showed a positive sign in the physical examination of the distal radioulnar joint among the three groups at the final follow-up time points.Conclusion: When the DRUJ is stable, an untreated ulnar styloid fracture does not affect the wrist outcome of the patient with an unstable DRF treated with external fixation. [ABSTRACT FROM AUTHOR]- Published
- 2013
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10. Prevalence of incidental thyroid abnormalities in patients with degenerative cervical spondylosis: a retrospective cross-sectional magnetic resonance imaging study.
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Yan ZW, Li DY, Jin WY, Huang CR, Pan S, Peng DL, Zhang XC, Pang Y, Guo KJ, and Zheng X
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Background: Incidental thyroid abnormalities found on magnetic resonance imaging (MRI) of the neck are not uncommon. This study aimed to investigate the prevalence of incidental thyroid abnormalities in the cervical spine MRI of the degenerative cervical spondylosis (DCS) population indicated for surgery and to identify patients who require additional workup based on the recommendations of the American College of Radiology (ACR)., Methods: All consecutive patients with DCS and indications for cervical spine surgery from October 2014 to May 2019 in the Affiliated Hospital of Xuzhou Medical University were reviewed. All MRI scans of the cervical spine routinely include the thyroid. Cervical spine MRI scans were retrospectively evaluated for the prevalence, size, morphologic characteristics, and location of incidental thyroid abnormalities., Results: A total of 1,313 patients were included in the analysis, 98 (7.5%) of whom were found to have incidental thyroid abnormalities. The most frequent thyroid abnormality was thyroid nodules (5.3%), followed by goiters (1.4%). Other thyroid abnormalities included Hashimoto thyroiditis (0.4%) and thyroid cancer (0.5%). There was a statistically significant difference in age and sex between patients with DCS with and without incidental thyroid abnormalities (P=0.018 and P=0.007). Stratified by age, the results showed that the highest incidence of incidental thyroid abnormalities was found in patients aged 71 to 80 years (12.4%). Eighteen patients (1.4%) needed further ultrasound (US) and relevant workups., Conclusions: Incidental thyroid abnormalities are common in cervical MRI, with a prevalence of 7.5% identified in patients with DCS. Incidental thyroid abnormalities are large or have suspicious imaging features, and further evaluation with a dedicated thyroid US examination should be completed before cervical spine surgery is undertaken., Competing Interests: Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at https://qims.amegroups.com/article/view/10.21037/qims-22-484/coif). The authors have no conflicts of interest to declare., (2023 Quantitative Imaging in Medicine and Surgery. All rights reserved.)
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- 2023
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11. Lymphadenopathy in POEMS syndrome: a correlation between clinical features and imaging findings.
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Shi XF, Hu SD, Wu LL, Chen XY, Wu JN, Yu XQ, Li DY, Chen M, Liu YC, Zhu Y, and Xi XD
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Lymphadenopathy is an important characteristic of POEMS syndrome, and a Castleman disease (CD)-like pathologic change in the lymph nodes is one of the major diagnostic criteria. However, the characteristics of lymphadenopathy in POEMS still have not been completely elucidated. The lymph node biopsies are available only for a small proportion of patients. A simple and safe way is needed to rule CD in or out. This study aimed to analyse the features of lymphadenopathy and estimate the role of imaging methods, including computed tomography (CT) and positron emission tomography-CT (PET/CT), in the diagnosis of lymphadenopathy in patients with POEMS syndrome. We conducted a retrospective analysis of 23 patients with confirmed POEMS syndrome. All of the patients received chest and abdominal CT scan and/or superficial ultrasound examinations. Four patients underwent PET/CT examinations, and 6 patients received lymph node biopsies. Enlarged lymph nodes (short diameter ≥ 1 cm) were found in 48% (11/23) of patients, but only 1 patient had an enlarged lymph node with a diameter ≥ 2 cm. Lymph nodes with CD-like pathologic changes from 2 patients showed increased maximum standard uptake values (SUV
max ) of18 F-deoxyglucose (18 FDG) on PET/CT, while lymph nodes with reactive pathologic changes from 2 other patients showed a normal metabolic PET/CT profile. The extent of lymph node enlargement in patients with POEMS was less than that in patients with CD per se . We draw the conclusion that most of the enlarged lymph nodes had diameters ≤ 2 cm, which is less than that in cases of CD per se and PET/CT may be helpful in determining whether enlarged lymph nodes are characterized by CD-like changes or not., Competing Interests: None., (IJCEP Copyright © 2020.)- Published
- 2020
12. Upregulation of P63 inhibits chondrocyte autophagy thereby enhancing the malignant progression of osteoarthritis.
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Wangyang Y, Zheng X, Liu GW, Li DY, Feng YB, Guo TY, Ma C, and Wang T
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- Adenine analogs & derivatives, Adenine pharmacology, Aged, Blotting, Western, Cartilage, Articular pathology, Case-Control Studies, Disease Progression, Female, Humans, Male, Microscopy, Electron, Transmission, Middle Aged, Osteoarthritis genetics, Time Factors, Transfection, Up-Regulation, Autophagy genetics, Chondrocytes pathology, Osteoarthritis pathology, Transcription Factors genetics, Tumor Suppressor Proteins genetics
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Loss of autophagy is suggested to play a key role in the progression of osteoarthritis (OA). P63 is a member of the P53 family, which is widely dysregulated in various tumors. However, the specific role of P63 in chondrocyte autophagy has never been fully understood. Here, the expression level of P63 in the articular cartilages of OA patients and chondrocytes treated with 3-MA was explored using western blot. Autophagy was determined using transmission electron microscopy and mRFP-GFP-LC3 assay. Fewer autophagic vesicles were identified in the articular cartilages of OA patients compared with that of normal control. Both the mRNA and protein levels of P63 was markedly increased in the articular cartilages of OA patients compared with that of normal control. MTT assay demonstrated that P63 overexpression markedly reduced chondrocyte viability at 24, 36 and 48 h, while inhibition of P63 inhibited cell viability at 24, 36 and 48 h, respectively. Furthermore, autophagic flux assay showed that transfection of ad-P63 markedly decreased the yellow dots in chondrocytes, while inhibition of P63 induced chondrycyte autophagy. In summary, we first demonstrated that upregulation of P63 in the cartilage tissues of OA patients inhibited chondrocyte autophagy thereby contributing to the malignant progression of OA.
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- 2017
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