Disease Markers最新文献

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Retracted: Study on the Effect of MRI in the Diagnosis of Benign and Malignant Thoracic Tumors. 回顾性研究:MRI在胸部良恶性肿瘤诊断中的作用。
4区 医学
Disease Markers Pub Date : 2023-07-12 eCollection Date: 2023-01-01 DOI: 10.1155/2023/9767143
Disease Markers
{"title":"Retracted: Study on the Effect of MRI in the Diagnosis of Benign and Malignant Thoracic Tumors.","authors":"Disease Markers","doi":"10.1155/2023/9767143","DOIUrl":"10.1155/2023/9767143","url":null,"abstract":"<p><p>[This retracts the article DOI: 10.1155/2021/3265561.].</p>","PeriodicalId":11201,"journal":{"name":"Disease Markers","volume":"2023 ","pages":"9767143"},"PeriodicalIF":0.0,"publicationDate":"2023-07-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10356411/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9848135","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Retracted: A Comprehensive Bioinformatic Analysis of NOTCH Pathway Involvement in Stomach Adenocarcinoma. 撤回:NOTCH通路参与胃癌的综合生物信息学分析。
4区 医学
Disease Markers Pub Date : 2023-07-12 eCollection Date: 2023-01-01 DOI: 10.1155/2023/9895230
Disease Markers
{"title":"Retracted: A Comprehensive Bioinformatic Analysis of NOTCH Pathway Involvement in Stomach Adenocarcinoma.","authors":"Disease Markers","doi":"10.1155/2023/9895230","DOIUrl":"10.1155/2023/9895230","url":null,"abstract":"<p><p>[This retracts the article DOI: 10.1155/2021/4739868.].</p>","PeriodicalId":11201,"journal":{"name":"Disease Markers","volume":"2023 ","pages":"9895230"},"PeriodicalIF":0.0,"publicationDate":"2023-07-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10356479/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9848138","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Retracted: Introducing V-Line as a New Strategy to Choose Surgical Corridor in Oblique Lumbar Interbody Fusion at the L5-S1 Segment. 回缩:引入V型线作为L5-S1段斜交腰段融合术中选择手术通道的新策略。
4区 医学
Disease Markers Pub Date : 2023-07-12 eCollection Date: 2023-01-01 DOI: 10.1155/2023/9839325
Disease Markers
{"title":"Retracted: Introducing V-Line as a New Strategy to Choose Surgical Corridor in Oblique Lumbar Interbody Fusion at the L5-S1 Segment.","authors":"Disease Markers","doi":"10.1155/2023/9839325","DOIUrl":"10.1155/2023/9839325","url":null,"abstract":"<p><p>[This retracts the article DOI: 10.1155/2021/5584372.].</p>","PeriodicalId":11201,"journal":{"name":"Disease Markers","volume":"2023 ","pages":"9839325"},"PeriodicalIF":0.0,"publicationDate":"2023-07-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10356478/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9848137","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Retracted: Alterations of Several Serum Parameters Are Associated with Preeclampsia and May Be Potential Markers for the Assessment of PE Severity. 收回:几种血清参数的改变与先兆子痫有关,可能是评估PE严重程度的潜在标志物。
4区 医学
Disease Markers Pub Date : 2023-07-12 eCollection Date: 2023-01-01 DOI: 10.1155/2023/9843085
Disease Markers
{"title":"Retracted: Alterations of Several Serum Parameters Are Associated with Preeclampsia and May Be Potential Markers for the Assessment of PE Severity.","authors":"Disease Markers","doi":"10.1155/2023/9843085","DOIUrl":"10.1155/2023/9843085","url":null,"abstract":"<p><p>[This retracts the article DOI: 10.1155/2020/7815214.].</p>","PeriodicalId":11201,"journal":{"name":"Disease Markers","volume":"2023 ","pages":"9843085"},"PeriodicalIF":0.0,"publicationDate":"2023-07-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10356431/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9848139","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Retracted: Environmental and Genetic Factors in the Pathogenesis of COPD in the Road-Working Population. 收回:道路作业人群COPD发病机制中的环境和遗传因素。
4区 医学
Disease Markers Pub Date : 2023-07-12 eCollection Date: 2023-01-01 DOI: 10.1155/2023/9759372
Disease Markers
{"title":"Retracted: Environmental and Genetic Factors in the Pathogenesis of COPD in the Road-Working Population.","authors":"Disease Markers","doi":"10.1155/2023/9759372","DOIUrl":"10.1155/2023/9759372","url":null,"abstract":"<p><p>[This retracts the article DOI: 10.1155/2021/9953234.].</p>","PeriodicalId":11201,"journal":{"name":"Disease Markers","volume":"2023 ","pages":"9759372"},"PeriodicalIF":0.0,"publicationDate":"2023-07-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10356519/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9840797","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Retracted: Distinct Urinary Metabolic Biomarkers of Human Colorectal Cancer. 撤回:人类癌症大肠癌的独特尿代谢生物标志物。
4区 医学
Disease Markers Pub Date : 2023-07-12 eCollection Date: 2023-01-01 DOI: 10.1155/2023/9873530
Disease Markers
{"title":"Retracted: Distinct Urinary Metabolic Biomarkers of Human Colorectal Cancer.","authors":"Disease Markers","doi":"10.1155/2023/9873530","DOIUrl":"10.1155/2023/9873530","url":null,"abstract":"<p><p>[This retracts the article DOI: 10.1155/2022/1758113.].</p>","PeriodicalId":11201,"journal":{"name":"Disease Markers","volume":"2023 ","pages":"9873530"},"PeriodicalIF":0.0,"publicationDate":"2023-07-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10356303/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9840799","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Cuproptosis-Related Genes CDK1 and COA6 Involved in the Prognosis Prediction of Liver Hepatocellular Carcinoma. 参与肝肝细胞癌预后预测的杯突相关基因 CDK1 和 COA6
4区 医学
Disease Markers Pub Date : 2023-05-11 eCollection Date: 2023-01-01 DOI: 10.1155/2023/5552798
Sanfeng Han, Tao Ye, Yuqin Mao, Bo Hu, Chen Wang
{"title":"Cuproptosis-Related Genes CDK1 and COA6 Involved in the Prognosis Prediction of Liver Hepatocellular Carcinoma.","authors":"Sanfeng Han, Tao Ye, Yuqin Mao, Bo Hu, Chen Wang","doi":"10.1155/2023/5552798","DOIUrl":"10.1155/2023/5552798","url":null,"abstract":"<p><strong>Background: </strong>Liver hepatocellular carcinoma (LIHC) is the most frequently seen type of primary liver cancer. Cuproptosis is a novel form of cell death highly associated with mitochondrial metabolism. However, the clinical impact and pertinent mechanism of cuproptosis genes in LIHC remain largely unknown.</p><p><strong>Methods: </strong>From public databases, we systematically assessed common genes from LIHC differentially expressed genes (DEGs) and cuproptosis-related genes using bioinformatics analysis. These common genes were then analyzed by enrichment analysis, mutation analysis, risk score model, and others to find candidate hub genes related to LIHC and cuproptosis. Next, hub genes were determined by expression, clinical factors, immunoassay, and prognostic nomogram.</p><p><strong>Results: </strong>Based on 129 cuproptosis-related genes and 3492 LIHC DEGs, we totally identified 21 downregulated and 18 upregulated common genes, and they were enriched in pathways, such as zinc ion homeostasis and oxidative phosphorylation. In the mutation analysis, missense mutation was the most common type in LIHC patients, and the common gene F5 had the highest mutation frequency. After LASSO-Cox regression analysis and prognostic analysis, CDK1, ABCB6, LCAT, and COA6 were identified as prognostic signature genes. Among them, ABCB6 and LCAT were lowly expressed in tumors, and CDK1 and COA6 were highly expressed in tumors. In addition, ABCB6 and LCAT were negatively correlated with 6 kinds of immune cells, while CDK1 and COA6 were positively correlated with them. CDK1 and COA6 were identified as hub genes related to LIHC by Cox regression analysis and prognostic nomogram.</p><p><strong>Conclusion: </strong>CDK1 and COA6 are two oncogenes in LIHC, which are involved in the molecular mechanism of cuproptosis and LIHC. Besides, CDK1 and COA6 can positively regulate the expressions of immune cells in LIHC. In clinical practice, they can be used as immunotherapeutic targets and prognostic predictors in LIHC, which sheds new light on the scientific fields of cuproptosis and LIHC.</p>","PeriodicalId":11201,"journal":{"name":"Disease Markers","volume":"2023 ","pages":"5552798"},"PeriodicalIF":0.0,"publicationDate":"2023-05-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10195163/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10489921","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Treatment with Antiviral Drugs Will Significantly Inhibit the HIV-1 RNA POL Gene Expression and Viral Load in AIDS Patients. 抗病毒药物治疗将显著抑制艾滋病患者的 HIV-1 RNA POL 基因表达和病毒载量。
4区 医学
Disease Markers Pub Date : 2023-04-14 eCollection Date: 2023-01-01 DOI: 10.1155/2023/9910542
Penghui Shi, Xiaodong Wang, Miaomiao Su, Juan Meng, Hao Wang, Weiguang Fan
{"title":"Treatment with Antiviral Drugs Will Significantly Inhibit the HIV-1 RNA POL Gene Expression and Viral Load in AIDS Patients.","authors":"Penghui Shi, Xiaodong Wang, Miaomiao Su, Juan Meng, Hao Wang, Weiguang Fan","doi":"10.1155/2023/9910542","DOIUrl":"10.1155/2023/9910542","url":null,"abstract":"<p><strong>Objective: </strong>This study is to investigate the difference in HIV-1 RNA pol gene expression in AIDS patients before and after antiviral treatment and its effect on the expression level of CD4<sup>+</sup>/CD8<sup>+</sup> T cells in peripheral blood.</p><p><strong>Methods: </strong>The participants included 200 AIDS patients who had undergone antiviral medication, and the quantity of HIV-1 RNA pol gene was determined using nested polymerase chain reaction (nPCR). The levels of CD3+, CD4+, and CD8+ T lymphocytes in peripheral blood were measured by flow cytometry before and after therapy. The receiver operating characteristics (ROC) curve was used to assess the impact of HIV-1 RNA pol gene expression and the CD4+/CD8+ ratio on the prognosis of AIDS patients.</p><p><strong>Results: </strong>After three months of therapy, the levels of HIV-1 RNA and viral load in the patients showed a drastic decline, while the levels of CD4+/CD8+ were markedly elevated (<i>P</i> < 0.05). Logistic analysis revealed that patients' viral loads were positively correlated with HIV-1 RNA and negatively correlated with CD4+/CD8+ (<i>P</i> < 0.05). The alanine aminotransferase (ALT), white blood cell (WBC) count, Serum creatinine (Cr), total cholesterol (TC), triglyceride (TG), and platelet (PLT) levels significantly increased following a 24-month therapy, while no significant changes were observed in the level of aspartate aminotransferase (AST), red blood cell (RBC), and neutrophil (NEU) (%). (<i>P</i> > 0.05).</p><p><strong>Conclusion: </strong>Antiviral drugs significantly inhibit the HIV-1 RNA POL gene expression and viral load in AIDS patients but upregulate the expression level of CD4<sup>+</sup>/CD8<sup>+</sup> T cells in peripheral blood.</p>","PeriodicalId":11201,"journal":{"name":"Disease Markers","volume":"2023 ","pages":"9910542"},"PeriodicalIF":0.0,"publicationDate":"2023-04-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10121356/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9445398","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The Identification and Clinical Value Evaluation of CYCS Related to Asthma through Bioinformatics Analysis and Functional Experiments. 通过生物信息学分析和功能实验鉴定与哮喘相关的 CYCS 并评估其临床价值。
4区 医学
Disease Markers Pub Date : 2023-04-14 eCollection Date: 2023-01-01 DOI: 10.1155/2023/5746940
Yan Li, Li Li, Hua Zhao, Xiwen Gao, Shanqun Li
{"title":"The Identification and Clinical Value Evaluation of CYCS Related to Asthma through Bioinformatics Analysis and Functional Experiments.","authors":"Yan Li, Li Li, Hua Zhao, Xiwen Gao, Shanqun Li","doi":"10.1155/2023/5746940","DOIUrl":"10.1155/2023/5746940","url":null,"abstract":"<p><strong>Background: </strong>Asthma is one of the most common respiratory diseases and one of the largest burdens of health care resources across the world. This study is aimed at using bioinformatics methods to find effective clinical indicators for asthma and conducting experimental validation.</p><p><strong>Methods: </strong>We downloaded GSE64913 data and performed differentially expressed gene (DEG) screening. Weighted gene coexpression network analysis (WGCNA) on DEGs was applied to identify key module most associated with asthma for protein-protein interaction (PPI) analysis. According to the degree value, ten genes were obtained and subjected to expression analysis and receiver operating characteristic (ROC) analysis. Next, key genes were screened for expression analysis and immunological analysis. Finally, cell counting kit-8 (CCK-8) and qRT-PCR were also conducted to observe the influence of hub gene on cell proliferation and inflammatory cytokines.</p><p><strong>Results: </strong>From the GSE64913 dataset, 711 upregulated and 684 downregulated DEGs were found. In WGCNA, the top 10 genes in the key module were examined by expression analysis in asthma, and CYCS was determined as an asthma-related oncogene with a good predictive ability for the prognosis of asthmatic patients. CYCS is significantly associated with immune cells, such as HHLA2, IDO1, TGFBR1, and CCL18 and promoted the proliferation of asthmatic cells in vitro.</p><p><strong>Conclusion: </strong>CYCS plays an oncogenic role in the pathophysiology of asthma, indicating that this gene may become a novel diagnostic biomarker and promising target of asthma treatment.</p>","PeriodicalId":11201,"journal":{"name":"Disease Markers","volume":"2023 ","pages":"5746940"},"PeriodicalIF":0.0,"publicationDate":"2023-04-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10121352/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9445395","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Identification of Inflammatory Gene in the Congenital Heart Surgery Patients following Cardiopulmonary Bypass via the Way of WGCNA and Machine Learning Algorithms. 应用WGCNA和机器学习算法鉴定先天性心脏手术患者体外循环后炎症基因
4区 医学
Disease Markers Pub Date : 2023-04-12 eCollection Date: 2023-01-01 DOI: 10.1155/2023/5493415
Liang Cai, Bingdong Zhang
{"title":"Identification of Inflammatory Gene in the Congenital Heart Surgery Patients following Cardiopulmonary Bypass via the Way of WGCNA and Machine Learning Algorithms.","authors":"Liang Cai, Bingdong Zhang","doi":"10.1155/2023/5493415","DOIUrl":"10.1155/2023/5493415","url":null,"abstract":"<p><p>Performing cardiopulmonary bypass (CPB) to reduce ischemic injury during surgery is a common approach to cardiac surgery. However, this procedure can lead to systemic inflammation and multiorgan dysfunction. Therefore, elucidating the molecular mechanisms of CPB-induced inflammatory cytokine release is essential as a critical first step in identifying new targets for therapeutic intervention. The GSE143780 dataset which is mRNA sequencing from total circulating leukocytes of the neonatorum was downloaded from the Gene Expression Omnibus (GEO) database. A total of 21 key module genes were obtained by analyzing the intersection of differentially expressed gene (DEG) and gene coexpression network analysis (WGCNA), and then, 4 genes (TRAF3IP2-AS1, PPARGC1B, CD4, and PDLIM5) were further confirmed after the least absolute shrinkage and selection operator (LASSO) and support vector machine recursive feature elimination (SVM-RFE) screening and were used as hub genes for CPB-induced inflammatory cytokine release in patients with congenital heart defects. The enrichment analysis revealed 21 key module genes mainly related to the functions of developmental cell growth, regulation of monocyte differentiation, regulation of myeloid leukocyte differentiation, ERK1 and ERK2 cascade, volume-sensitive anion channel activity, and estrogen receptor binding. The result of gene set enrichment analysis (GSEA) showed that the hub genes were related to different physiological functions of cells. The ceRNA network established for hub genes includes 3 hub genes (PPARGC1B, CD4, and PDLIM5), 55 lncRNAs, and 34 miRNAs. In addition, 4 hub genes have 215 potential therapeutic agents. Finally, expression validation of the four hub genes revealed that they were all significantly low expressed in the surgical samples than before.</p>","PeriodicalId":11201,"journal":{"name":"Disease Markers","volume":"1 1","pages":"5493415"},"PeriodicalIF":0.0,"publicationDate":"2023-04-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11401684/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43852390","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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