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

被引:11
|
作者
Balakittnen, Jaikrishna [1 ,2 ]
Weeramange, Chameera Ekanayake [1 ,3 ]
Wallace, Daniel F. [4 ]
Duijf, Pascal H. G. [5 ,6 ,7 ,8 ]
Cristino, Alexandre S. [9 ]
Hartel, Gunter [10 ,11 ,12 ]
Barrero, Roberto A. [13 ]
Taheri, Touraj [14 ,15 ]
Kenny, Liz [15 ,16 ]
Vasani, Sarju [1 ,16 ,17 ]
Batstone, Martin [18 ]
Breik, Omar [16 ,18 ]
Punyadeera, Chamindie [1 ,3 ]
机构
[1] Griffith Univ, Griffith Inst Drug Discovery, Saliva & Liquid Biopsy Translat Lab, Nathan, Qld, Australia
[2] Univ Jaffna, Fac Allied Hlth Sci, Dept Med Lab Sci, Jaffna, Sri Lanka
[3] Griffith Univ, Menzies Hlth Inst, Gold Coast, Qld, Australia
[4] Queensland Univ Technol, Fac Hlth, Sch Biomed Sci, Brisbane, Qld, Australia
[5] Univ South Australia, Ctr Canc Biol Clin & Hlth Sci, Adelaide, SA, Australia
[6] SA Pathol, Adelaide, SA, Australia
[7] Univ Oslo, Inst Clin Med, Fac Med, Oslo, Norway
[8] Oslo Univ Hosp, Dept Med Genet, Oslo, Norway
[9] Griffith Univ, Griffith Inst Drug Discovery, Nathan, Qld, Australia
[10] QIMR Berghofer Med Res Inst, Stat Unit, Brisbane, Qld, Australia
[11] Univ Queensland, Sch Publ Hlth, Brisbane, Qld, Australia
[12] Queensland Univ Technol, Sch Nursing, Brisbane, Qld, Australia
[13] Queensland Univ Technol, Acad Div, eres, Res Infrastruct, Brisbane, Qld, Australia
[14] Royal Brisbane & Womens Hosp, Dept Anat Pathol, Herston, Qld, Australia
[15] Univ Queensland, Fac Med, Brisbane, Qld, Australia
[16] Royal Brisbane & Womens Hosp, Canc Care Serv, Herston, Qld, Australia
[17] Royal Brisbane & Womens Hosp, Dept Otolaryngol, Herston, Qld, Australia
[18] Royal Brisbane & Womens Hosp, Dept Oral & Maxillofacial Surg, Herston, Qld, Australia
基金
英国医学研究理事会;
关键词
SQUAMOUS-CELL CARCINOMA; MICRORNAS; BIOMARKER;
D O I
10.1038/s41368-023-00273-w
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
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.
引用
收藏
页数:13
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