Benedikt Ewig , Thomas Büttner , Glen Kristiansen , Doris Schmidt , Jörg Ellinger , Stefan Hauser
{"title":"微rna 193a-3p、378-3p、210-3p和362-3p作为透明细胞肾细胞癌血清生物标志物的潜力","authors":"Benedikt Ewig , Thomas Büttner , Glen Kristiansen , Doris Schmidt , Jörg Ellinger , Stefan Hauser","doi":"10.1016/j.humgen.2025.201444","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><div>MicroRNAs (miRs) play a significant role in carcinogenesis and tumor progression, suggesting their potential as biomarkers. This study aimed to evaluate the diagnostic utility of four circulating miRs in patients with clear cell renal cell carcinoma (ccRCC).</div></div><div><h3>Methods</h3><div>Serum expression levels of miR-193a-3p, miR-378-3p, miR-210-3p, and miR-362-3p were quantified in 30 patients with clear cell renal cell carcinoma (ccRCC) and 15 non-tumor controls using real-time polymerase chain reaction. Mann–Whitney <em>U</em> tests and Receiver Operating Characteristics with Area under the curve (AUC) calculations were employed to evaluate the association between miR expression levels and patient group (ccRCC versus controls).</div></div><div><h3>Results</h3><div>Statistically significant differences in mean serum levels of miR-193a-3p and miR-378-3p were observed between ccRCC patients and controls. The median miR-193a-3p level was increased in ccRCC patients (median: 4.50 %, IQR: 1.38, 11.47) compared to controls (median: 2.57 %, IQR: 0.27, 3.87), <em>p</em> = 0.032; AUC for ccRCC detection was 0.70. Also, the median miR-378-3p level was higher in ccRCC patients (median: 2.01 %, IQR: 1.00, 3.33) compared to controls (median: 0.66 %, IQR: 0.44, 1.98), <em>p</em> = 0.049. AUC was 0.68. No significant differences were found for serum miR-362-3p and miR-210-3p expression in ccRCC patients and non-tumor controls (<em>p</em> = 0.547 for miR-362-3p and <em>p</em> = 0.791 for miR-210-3p).</div></div><div><h3>Conclusion</h3><div>These findings suggest that miR-193a-3p and miR-378-3p may have limited potential as diagnostic biomarkers for ccRCC. The data do not support further investigation of miR-362-3p and miR-210-3p for this purpose.</div></div>","PeriodicalId":29686,"journal":{"name":"Human Gene","volume":"45 ","pages":"Article 201444"},"PeriodicalIF":0.5000,"publicationDate":"2025-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Potential of micro-RNAs 193a-3p, 378-3p, 210-3p, and 362-3p as serum biomarkers for clear cell renal cell carcinoma\",\"authors\":\"Benedikt Ewig , Thomas Büttner , Glen Kristiansen , Doris Schmidt , Jörg Ellinger , Stefan Hauser\",\"doi\":\"10.1016/j.humgen.2025.201444\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Objective</h3><div>MicroRNAs (miRs) play a significant role in carcinogenesis and tumor progression, suggesting their potential as biomarkers. This study aimed to evaluate the diagnostic utility of four circulating miRs in patients with clear cell renal cell carcinoma (ccRCC).</div></div><div><h3>Methods</h3><div>Serum expression levels of miR-193a-3p, miR-378-3p, miR-210-3p, and miR-362-3p were quantified in 30 patients with clear cell renal cell carcinoma (ccRCC) and 15 non-tumor controls using real-time polymerase chain reaction. Mann–Whitney <em>U</em> tests and Receiver Operating Characteristics with Area under the curve (AUC) calculations were employed to evaluate the association between miR expression levels and patient group (ccRCC versus controls).</div></div><div><h3>Results</h3><div>Statistically significant differences in mean serum levels of miR-193a-3p and miR-378-3p were observed between ccRCC patients and controls. The median miR-193a-3p level was increased in ccRCC patients (median: 4.50 %, IQR: 1.38, 11.47) compared to controls (median: 2.57 %, IQR: 0.27, 3.87), <em>p</em> = 0.032; AUC for ccRCC detection was 0.70. Also, the median miR-378-3p level was higher in ccRCC patients (median: 2.01 %, IQR: 1.00, 3.33) compared to controls (median: 0.66 %, IQR: 0.44, 1.98), <em>p</em> = 0.049. AUC was 0.68. No significant differences were found for serum miR-362-3p and miR-210-3p expression in ccRCC patients and non-tumor controls (<em>p</em> = 0.547 for miR-362-3p and <em>p</em> = 0.791 for miR-210-3p).</div></div><div><h3>Conclusion</h3><div>These findings suggest that miR-193a-3p and miR-378-3p may have limited potential as diagnostic biomarkers for ccRCC. The data do not support further investigation of miR-362-3p and miR-210-3p for this purpose.</div></div>\",\"PeriodicalId\":29686,\"journal\":{\"name\":\"Human Gene\",\"volume\":\"45 \",\"pages\":\"Article 201444\"},\"PeriodicalIF\":0.5000,\"publicationDate\":\"2025-06-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Human Gene\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2773044125000701\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Human Gene","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2773044125000701","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0
摘要
目的:micrornas (miRs)在癌变和肿瘤进展中发挥重要作用,提示其作为生物标志物的潜力。本研究旨在评估四种循环miRs在透明细胞肾细胞癌(ccRCC)患者中的诊断价值。方法采用实时聚合酶链反应法测定30例透明细胞肾细胞癌(ccRCC)患者和15例非肿瘤对照组血清中miR-193a-3p、miR-378-3p、miR-210-3p和miR-362-3p的表达水平。采用Mann-Whitney U检验和曲线下面积(AUC)计算的受试者操作特征来评估miR表达水平与患者组(ccRCC与对照组)之间的关系。结果ccRCC患者血清miR-193a-3p、miR-378-3p水平与对照组比较差异均有统计学意义。与对照组(中位数:2.57%,IQR: 0.27, 3.87)相比,ccRCC患者中位miR-193a-3p水平升高(中位数:4.50%,IQR: 1.38, 11.47), p = 0.032;ccRCC检测的AUC为0.70。此外,ccRCC患者中位miR-378-3p水平(中位数:2.01%,IQR: 1.00, 3.33)高于对照组(中位数:0.66%,IQR: 0.44, 1.98), p = 0.049。AUC为0.68。血清miR-362-3p和miR-210-3p在ccRCC患者和非肿瘤对照组中表达无显著差异(miR-362-3p p = 0.547, miR-210-3p p = 0.791)。这些发现表明miR-193a-3p和miR-378-3p作为ccRCC的诊断生物标志物可能潜力有限。数据不支持为此目的进一步研究miR-362-3p和miR-210-3p。
Potential of micro-RNAs 193a-3p, 378-3p, 210-3p, and 362-3p as serum biomarkers for clear cell renal cell carcinoma
Objective
MicroRNAs (miRs) play a significant role in carcinogenesis and tumor progression, suggesting their potential as biomarkers. This study aimed to evaluate the diagnostic utility of four circulating miRs in patients with clear cell renal cell carcinoma (ccRCC).
Methods
Serum expression levels of miR-193a-3p, miR-378-3p, miR-210-3p, and miR-362-3p were quantified in 30 patients with clear cell renal cell carcinoma (ccRCC) and 15 non-tumor controls using real-time polymerase chain reaction. Mann–Whitney U tests and Receiver Operating Characteristics with Area under the curve (AUC) calculations were employed to evaluate the association between miR expression levels and patient group (ccRCC versus controls).
Results
Statistically significant differences in mean serum levels of miR-193a-3p and miR-378-3p were observed between ccRCC patients and controls. The median miR-193a-3p level was increased in ccRCC patients (median: 4.50 %, IQR: 1.38, 11.47) compared to controls (median: 2.57 %, IQR: 0.27, 3.87), p = 0.032; AUC for ccRCC detection was 0.70. Also, the median miR-378-3p level was higher in ccRCC patients (median: 2.01 %, IQR: 1.00, 3.33) compared to controls (median: 0.66 %, IQR: 0.44, 1.98), p = 0.049. AUC was 0.68. No significant differences were found for serum miR-362-3p and miR-210-3p expression in ccRCC patients and non-tumor controls (p = 0.547 for miR-362-3p and p = 0.791 for miR-210-3p).
Conclusion
These findings suggest that miR-193a-3p and miR-378-3p may have limited potential as diagnostic biomarkers for ccRCC. The data do not support further investigation of miR-362-3p and miR-210-3p for this purpose.