基于唾液的新型 miRNA 图谱可用于诊断和预测口腔癌。

IF 10.8 1区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE International Journal of Oral Science Pub Date : 2024-02-18 DOI:10.1038/s41368-023-00273-w
Jaikrishna Balakittnen, Chameera Ekanayake Weeramange, Daniel F Wallace, Pascal H G Duijf, Alexandre S Cristino, Gunter Hartel, Roberto A Barrero, Touraj Taheri, Liz Kenny, Sarju Vasani, Martin Batstone, Omar Breik, Chamindie Punyadeera
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引用次数: 0

摘要

口腔癌(OC)是最常见的头颈部癌症。尽管口腔癌发病率高,对患者的预后不利,但目前还没有用于早期检测口腔癌的生物标志物。本研究旨在发现、开发和验证一种基于唾液的新型 microRNA 标志,用于口腔潜在恶性疾病(OPMD)的早期诊断和 OC 风险预测。研究利用癌症基因组图谱(TCGA)的miRNA测序数据和唾液样本的小RNA测序数据来发现差异表达的miRNA。利用定量实时 PCR 技术在 OC(n = 50)、OPMD(n = 52)和对照组(n = 60)的唾液样本中验证了识别出的 miRNA。在发现阶段发现并验证了八个差异表达的 miRNA(miR-7-5p、miR-10b-5p、miR-182-5p、miR-215-5p、miR-431-5p、miR-486-3p、miR-3614-5p 和 miR-4707-3p)。我们的 8 个 miRNA 标志区分 OC 和对照组的效率为:曲线下面积(AUC)为 0.954,灵敏度为 86%:0.954,灵敏度:86%,特异性:90%,阳性预测值(PPV):87.8%,阴性预测值(PPV):87.8%:87.8%,阴性预测值 (NPV):88.5%:88.5%,而 OC 和 OPMD 之间的差异为AUC:灵敏度:90%,特异性:82.7%,PPV:74.2%,NPV:89.6%。我们制定了一个风险概率评分,以预测 OPMD 患者是否存在 OC 或 OC 的风险。我们建立的唾液 miRNA 特征可帮助诊断和预测 OC,从而彻底改变 OPMD 患者的治疗方法。我们的研究结果为利用唾液miRNA管理OC提供了新的思路,也为利用从唾液样本中提取的miRNA的临床实用性提供了新的思路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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A novel saliva-based miRNA profile to diagnose and predict oral cancer.

Oral cancer (OC) is the most common form of head and neck cancer. Despite the high incidence and unfavourable patient outcomes, currently, there are no biomarkers for the early detection of OC. This study aims to discover, develop, and validate a novel saliva-based microRNA signature for early diagnosis and prediction of OC risk in oral potentially malignant disorders (OPMD). The Cancer Genome Atlas (TCGA) miRNA sequencing data and small RNA sequencing data of saliva samples were used to discover differentially expressed miRNAs. Identified miRNAs were validated in saliva samples of OC (n = 50), OPMD (n = 52), and controls (n = 60) using quantitative real-time PCR. Eight differentially expressed miRNAs (miR-7-5p, miR-10b-5p, miR-182-5p, miR-215-5p, miR-431-5p, miR-486-3p, miR-3614-5p, and miR-4707-3p) were identified in the discovery phase and were validated. The efficiency of our eight-miRNA signature to discriminate OC and controls was: area under curve (AUC): 0.954, sensitivity: 86%, specificity: 90%, positive predictive value (PPV): 87.8% and negative predictive value (NPV): 88.5% whereas between OC and OPMD was: AUC: 0.911, sensitivity: 90%, specificity: 82.7%, PPV: 74.2% and NPV: 89.6%. We have developed a risk probability score to predict the presence or risk of OC in OPMD patients. We established a salivary miRNA signature that can aid in diagnosing and predicting OC, revolutionising the management of patients with OPMD. Together, our results shed new light on the management of OC by salivary miRNAs to the clinical utility of using miRNAs derived from saliva samples.

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来源期刊
International Journal of Oral Science
International Journal of Oral Science DENTISTRY, ORAL SURGERY & MEDICINE-
CiteScore
31.80
自引率
1.30%
发文量
53
审稿时长
>12 weeks
期刊介绍: The International Journal of Oral Science covers various aspects of oral science and interdisciplinary fields, encompassing basic, applied, and clinical research. Topics include, but are not limited to: Oral microbiology Oral and maxillofacial oncology Cariology Oral inflammation and infection Dental stem cells and regenerative medicine Craniofacial surgery Dental material Oral biomechanics Oral, dental, and maxillofacial genetic and developmental diseases Craniofacial bone research Craniofacial-related biomaterials Temporomandibular joint disorder and osteoarthritis The journal publishes peer-reviewed Articles presenting new research results and Review Articles offering concise summaries of specific areas in oral science.
期刊最新文献
Organoids in the oral and maxillofacial region: present and future. Personalized bioceramic grafts for craniomaxillofacial bone regeneration An unexpected role of neurite outgrowth inhibitor A as regulator of tooth enamel formation Periodontitis impacts on thrombotic diseases: from clinical aspect to future therapeutic approaches. CREB3L1 deficiency impairs odontoblastic differentiation and molar dentin deposition partially through the TMEM30B.
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