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肝外胆管癌中循环miR-18a和miR-532水平

Circulating miR-18a and miR-532 Levels in Extrahepatic Cholangiocarcinoma.

作者信息

Orzan Rares Ilie, Țigu Adrian Bogdan, Nechita Vlad-Ionuț, Nistor Madalina, Agoston Renata, Gonciar Diana, Pojoga Cristina, Seicean Andrada

机构信息

3rd Department of Internal Medicine, "Iuliu Hatieganu" University of Medicine and Pharmacy, Victor Babes Street, No. 8, 400347 Cluj-Napoca, Romania.

Regional Institute of Gastroenterology and Hepatology, Croitorilor Street, No. 19-21, 400394 Cluj-Napoca, Romania.

出版信息

J Clin Med. 2024 Oct 17;13(20):6177. doi: 10.3390/jcm13206177.

DOI:10.3390/jcm13206177
PMID:39458127
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11509052/
Abstract

: Cholangiocarcinoma (CCA) is a highly aggressive cancer of the bile ducts with a poor prognosis and limited diagnostic markers. This study aims to investigate the potential of miR-18a and miR-532 as biomarkers for CCA by exploring their correlations with clinical parameters and traditional tumor markers such as CA19.9, CEA, and AFP. : This study involved a cohort of patients diagnosed with CCA. Serum levels of miR-18a and miR-532 were measured and analyzed in relation to various clinical parameters, including age, tumor markers, and histological features. : Serum levels of miR-18a and miR-532 were upregulated in patients with extrahepatic cholangiocarcinoma (eCCA) compared to healthy controls ( < 0.05). MiR-18a and miR-532 levels were correlated with each other ( = 0.011, Spearman's rho = 0.482) but showed no significant correlation with age or traditional tumor markers (CA19.9, CEA, AFP). No significant differences in miR-18a and miR-532 levels were observed concerning tumor localization or histological grading. For predicting tumor resectability, miR-532 at a cut-off point of 2.12 showed a sensitivity of 72.73%, specificity of 81.25%, and an AUC of 71.3%, while miR-18a, at a cut-off of 1.83, had a sensitivity of 63.64%, specificity of 75%, and an AUC of 59.7%. ROC curve analysis suggested moderate diagnostic potential for miR-18a and miR-532, with AUC values of 0.64 and 0.689, respectively. : Although miR-18a and miR-532 showed significant upregulation in eCCA patients compared to healthy controls, they did not demonstrate significant associations with key clinical parameters, limiting their effectiveness as standalone diagnostic biomarkers. Further research involving larger, multi-center cohorts and additional molecular markers is necessary to validate these findings and explore the broader diagnostic potential of miRNAs in CCA.

摘要

胆管癌(CCA)是一种侵袭性很强的胆管癌症,预后较差且诊断标志物有限。本研究旨在通过探究miR-18a和miR-532与临床参数以及CA19.9、癌胚抗原(CEA)和甲胎蛋白(AFP)等传统肿瘤标志物的相关性,来研究它们作为CCA生物标志物的潜力。

本研究纳入了一组被诊断为CCA的患者。检测并分析了miR-18a和miR-532的血清水平与包括年龄、肿瘤标志物和组织学特征在内的各种临床参数的关系。

与健康对照相比,肝外胆管癌(eCCA)患者血清中miR-18a和miR-532水平上调(<0.05)。miR-18a和miR-532水平相互关联(P = 0.011,Spearman秩相关系数 = 0.482),但与年龄或传统肿瘤标志物(CA19.9、CEA、AFP)无显著相关性。在肿瘤定位或组织学分级方面,未观察到miR-18a和miR-532水平有显著差异。对于预测肿瘤可切除性,miR-532在截断点为2.12时,敏感性为72.73%,特异性为81.25%,曲线下面积(AUC)为71.3%,而miR-18a在截断点为1.83时,敏感性为63.64%,特异性为75%,AUC为59.7%。受试者工作特征(ROC)曲线分析表明,miR-18a和miR-532具有中等诊断潜力,AUC值分别为0.64和0.689。

虽然与健康对照相比,miR-18a和miR-532在eCCA患者中显著上调,但它们与关键临床参数无显著关联,限制了它们作为独立诊断生物标志物的有效性。有必要开展涉及更大规模多中心队列以及更多分子标志物的进一步研究,以验证这些发现,并探索miRNA在CCA中更广泛的诊断潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5279/11509052/05dd8aaa8489/jcm-13-06177-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5279/11509052/1b3a98b133d4/jcm-13-06177-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5279/11509052/c7da7189816f/jcm-13-06177-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5279/11509052/7cd2b577065d/jcm-13-06177-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5279/11509052/7127bfc2291e/jcm-13-06177-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5279/11509052/05dd8aaa8489/jcm-13-06177-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5279/11509052/1b3a98b133d4/jcm-13-06177-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5279/11509052/c7da7189816f/jcm-13-06177-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5279/11509052/7cd2b577065d/jcm-13-06177-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5279/11509052/7127bfc2291e/jcm-13-06177-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5279/11509052/05dd8aaa8489/jcm-13-06177-g005.jpg

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