A three-microRNA panel in serum as novel biomarker for papillary thyroid carcinoma diagnosis

被引:14
作者
Zou, Xuan [1 ]
Gao, Feng [2 ]
Wang, Zhi-Yan [3 ]
Zhang, Huo [4 ]
Liu, Qing-Xie [4 ]
Jiang, Lin [3 ]
Zhou, Xin [4 ]
Zhu, Wei [4 ]
机构
[1] Nanjing Med Univ, Clin Coll 1, Nanjing 210029, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Dept Orthoped, Affiliated Hosp 1, Nanjing 210029, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Dept Endocrinol & Metab, Affiliated Hosp 1, Nanjing 210029, Jiangsu, Peoples R China
[4] Nanjing Med Univ, Dept Oncol, Affiliated Hosp 1, Nanjing 210029, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
MicroRNA; Serum; Papillary thyroid carcinoma; Diagnosis; Biomarkers; FINE-NEEDLE-ASPIRATION; MIRNAS; MICRORNAS; MANAGEMENT; EXPRESSION; MECHANISM; PROFILES; NODULES; CANCER; MIR-25;
D O I
10.1097/CM9.0000000000001107
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Accumulating evidence has revealed that circulating microRNAs (miRNAs) can serve as non-invasive biomarkers for cancer diagnosis. This study aimed to identify differentially expressed miRNAs in serum which might become potential biomarkers for non-invasive diagnosis of papillary thyroid carcinoma (PTC). Methods The experiment was carried out between 2015 and 2017. In the screening stage, the Exiqon miRNA quantitative real-time polymerase chain reaction (qPCR) panel was applied to select candidate miRNAs. In the following training, testing, and external validation stages, the serum samples of 100 patients and 96 healthy controls (HCs) were analyzed to compare the expression levels of the identified miRNAs. The areas under the receiver operating characteristic curves (AUCs) were calculated to assess the diagnostic value of the identified signature. Results Three miRNAs (miR-25-3p, miR-296-5p, and miR-92a-3p) in serum were consistently up-regulated in PTC patients compared with HCs. A three-miRNA panel was constructed by logistic regression analysis and showed better diagnostic performance than a single miRNA for PTC detection. The AUCs of the panel were 0.727, 0.771, and 0.862 for the training, testing, and external validation stage, respectively. Meanwhile, the panel showed stable capability in differentiating PTC patients from patients with benign goiters, with an AUC as high as 0.969. For further exploration, the three identified miRNAs were analyzed in tissue samples (23 PTC vs. 23 HCs) and serum-derived exosomes samples (24 PTC vs. 24 HCs), and the altered expression in the tumor also indicated their close relationship with PTC disease. Conclusion We identify a three-miRNA panel in serum which might serve as a promising biomarker for PTC diagnosis.
引用
收藏
页码:2543 / 2551
页数:9
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