Differential expression levels of plasma microRNA in Hashimoto's disease

被引:13
|
作者
Zhao, Lijuan [1 ,2 ]
Zhou, Xin [3 ]
Shan, Xia [4 ]
Qi, Lian-wen [5 ,6 ]
Wang, Tongshan [3 ]
Zhu, Jun [7 ]
Zhu, Danxia [8 ]
Huan, Zebo [3 ]
Zhang, Lan [3 ]
Zhang, Huo [3 ]
Yin, Yin [9 ]
Wang, Zhiyan [1 ]
Zhu, Wei [3 ]
Cheng, Wenfang [10 ]
Jiang, Lin [1 ]
机构
[1] Nanjing Med Univ, Dept Endocrinol & Metab, Affiliated Hosp 1, 300 Guangzhou Rd, Nanjing 210029, Jiangsu, Peoples R China
[2] Puyang Municipal Anyang Area Hosp, Dept Endocrinol & Metab, 260 Dengta Rd, Anyang 455000, Henan, Peoples R China
[3] Nanjing Med Univ, Dept Oncol, Affiliated Hosp 1, 300 Guangzhou Rd, Nanjing 210029, Jiangsu, Peoples R China
[4] Nanjing Med Univ, Affiliated Jiangning Hosp, Dept Resp, Nanjing 210000, Jiangsu, Peoples R China
[5] China Pharmaceut Univ, State Key Lab Nat Med, 24 Tongjia Lane, Nanjing 210009, Jiangsu, Peoples R China
[6] China Pharmaceut Univ, Dept Pharmacognosy, 24 Tongjia Lane, Nanjing 210009, Jiangsu, Peoples R China
[7] Jiangsu Canc Hosp, Dept Radiat Oncol, 42 Bai Zi Ting, Nanjing 210009, Jiangsu, Peoples R China
[8] Soochow Univ, Dept Oncol, Affiliated Hosp 3, Changzhou 213003, Peoples R China
[9] Nanjing Med Univ, Dept Obstet & Gynecol, Affiliated Hosp 1, 300 Guangzhou Rd, Nanjing 210029, Jiangsu, Peoples R China
[10] Nanjing Med Univ, Dept Gastroenterol, Affiliated Hosp 1, 300 Guangzhou Rd, Nanjing 210029, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Circulating miRNA; Plasma microRNA; miRNA; Hashimoto's disease; Hashimoto's thyroiditis; HT; Diagnostic; Autoimmune; Thyroid; CIRCULATING MICRORNAS; THYROID-GLAND; IDENTIFICATION; CARCINOMA; CANCER; QUANTIFICATION; APOPTOSIS; OPERATION; BIOMARKER; SURVIVIN;
D O I
10.1016/j.gene.2017.10.053
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background: The altered expression of circulating miRNAs has been discovered in many autoimmune diseases (ADs). With rare existing research, it is still unclear in Hashimoto's thyroiditis (HT). We detected plasma miRNA expression of HT patients in this three-stage designed study. Methods: Differently expressed miRNAs (4 HT pools vs. 1 normal control pool) were identified using quantitative reverse transcription polymerase chain reaction (qRT-PCR) based Exiqon panel (miRCURY-Ready-to-Use- PCR-Human-panel-I + II-V1.M) in the initial discovery stage. These miRNAs were then confirmed in the training stage and further validated in the testing stage using qRT-PCR with 64 (32 HT vs. 32 NCs) and 136 samples (68 HT vs. 68 NCs), respectively. Results: A total of 10 miRNAs showed differential expression through the training stage. For further validation in the testing stage, expression of 6 miRNAs (miR-205, miR-20a-3p, miR-375, miR-296, miR-451, miR-500a) were consistent with those in the training stage. Combination results showed that these 6 miRNAs were significantly up-regulated in peripheral plasma of HT patients compared with normal controls (P < 0.05). In addition, the six-miRNA signature was evaluated to be a potential diagnostic marker of HT. The areas under the receiver operating characteristic curve of the signature were 0.80, 0.75 and 0.69 for the training, testing and the combined stages, respectively. Three miRNAs were associated with TSH levels in HT patients (miR-451, P = 0.043; naR-375, P = 0.043; miR-500a, P = 0.043). Additionally, miR-20a-3p was related with TgAb level (P = 0.046). Conclusions: We identified a miRNA signature including six dysregulated plasma miRNAs which could act as a diagnostic marker in plasma of HT, providing more evidence and better understanding for the association between circulating miRNAs and autoimmune diseases.
引用
收藏
页码:152 / 158
页数:7
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